Title of Invention	OXAZOLIDINONE DERIVATIVES WITH ANTIBIOTIC ACTIVITY
Abstract	Compounds of the formula (I), or a pharmaceutically accept-able salt, or an in-vivo-hydrolysable ester thereof, (1) wherein HET is an N-linked 5-membered heteroaryl ring, optionally substituted on a C atom by an oxo or thioxo group; and/or by 1 or 2 (l-4C)alkyl groups; and/or on an available nitrogen atom by (l-4C)alkyl; or HET is an N-linked 6-membered heteroaryl ring containing up to three nitrogen heteroatoms in total, optionally substituted on a C atom as above; Q is selected from, for example, Ql 01 R2 and R3 are independently hydrogen or fluoro; Tis selected from a range of groups, for example, of formula (TC5) (TC5) wherein Re is, for example, R13CO—, R13S02— or R13CS—; wherein R13 is, for example, optionally substituted (MOQalkyl or R14C(0)0(l-6C)alkyl wherein RJ4 is optionally substituted (l-10C)alkyl; are useful as antibacte-rial agents; and processes for their manufacture and phar-maceutical compositions containing them are described.

Title of Invention

OXAZOLIDINONE DERIVATIVES WITH ANTIBIOTIC ACTIVITY

Abstract

Compounds of the formula (I), or a pharmaceutically accept-able salt, or an in-vivo-hydrolysable ester thereof, (1) wherein HET is an N-linked 5-membered heteroaryl ring, optionally substituted on a C atom by an oxo or thioxo group; and/or by 1 or 2 (l-4C)alkyl groups; and/or on an available nitrogen atom by (l-4C)alkyl; or HET is an N-linked 6-membered heteroaryl ring containing up to three nitrogen heteroatoms in total, optionally substituted on a C atom as above; Q is selected from, for example, Ql 01 R2 and R3 are independently hydrogen or fluoro; Tis selected from a range of groups, for example, of formula (TC5) (TC5) wherein Re is, for example, R13CO—, R13S02— or R13CS—; wherein R13 is, for example, optionally substituted (MOQalkyl or R14C(0)0(l-6C)alkyl wherein RJ4 is optionally substituted (l-10C)alkyl; are useful as antibacte-rial agents; and processes for their manufacture and phar-maceutical compositions containing them are described.

Full Text	FORM 2 THE PATENTS ACT 1970 [39 OF 1970] COMPLETE SPECIFICATION [See Section 10, Rule 13] "OXAZOLIDINONE DERIVATIVES WITH ANTIBIOTIC ACTIVITY" ASTRAZENECA AB, a Swedish company of S-151 85 Sodertalje, Sweden, The following specification particularly describes the nature of the invention and the manner in which it is to be performed:- The present invention relates to antibiotic compounds and in particular to antibiotic compounds containing a substituted oxazolidmone ring. This invention further relates to processes for their preparation, to intermediates useful in their preparation, to their use as therapeutic agents and to pharmaceutical compositions containing them. The international microbiological community continues to express serious concern that the evolution of antibiotic resistance could result in strains against which currently available antibacterial agents will be ineffective. In general, bacterial pathogens may be classified as either Gram-positive or Gram-negative pathogens. Antibiotic compounds with effective activity against both Gram-positive and Gram-negative pathogens are generally regarded as having a broad spectrum of activity. The compounds of the present invention are regarded primarily as effective against Gram-positive pathogens because of their particularly good activity against such pathogens, but are also regarded as effective against certain Gram-negative pathogens. Gram-positive pathogens, for example Staphylococci, Enterococci, Streptococci and mycobacteria, are particularly important because of the development of resistant strains which are both difficult to treat and difficult to eradicate from the hospital environment once established. Examples of such strains are methicillin resistant staphylococcus (MRS A), methicillin resistant coagulase negative staphylococci (MRCNS), penicillin resistant Streptococcus pneumoniae and multiply resistant Enterococcus faecium. The major clinically effective antibiotic for treatment of such resistant Gram-positive pathogens is vancomycin. Vancomycin is a glycopeptide and is associated with nephrotoxicity and ototoxicity. Furthermore, and most importantly, antibacterial resistance to vancomycin and other glycopeptides is also appearing. This resistance is increasing at a steady rate rendering these agents less and less effective in the treatment of Gram-positive pathogens. There is also now increasing resistance appearing towards agents such as p -lactams, quinolones and macrolides used for the treatment of certain Gram negative strains responsible for upper respiratory tract infections. These strains include H.influenzae and M.catarrhalis. Certain antibacterial compounds containing an oxazolidinone ring have been described in the art (for example, Walter A. Gregory et al in J.Med.Chem. 1990, 33,2569-2578 and 1989, 32(8), 1673-81; Chung-Ho Park et al in J.Med.Chem. 1992, 35, 1156-1165). Such antibacterial oxazolidinone compounds with a 5-methylacetamide sidechain may be subject to mammalian peptidase metabolism. Furthermore, bacterial resistance to known antibacterial agents may develop, for example, by (i) the evolution of active binding sites in the bacteria rendering a previously active pharmacophore less effective or redundant, and/or (ii) the evolution of means to chemically deactivate a given pharmacophore. Therefore, there remains an ongoing need to find new antibacterial agents with a favourable pharmacological profile, in particular for compounds containing new pharmacophores. We have discovered a class of antibiotic compounds containing a new class of substituted oxazolidinone ring which has useful activity against Gram-positive pathogens including MRSA and MR.CNS and, in particular, against various strains exhibiting resistance to vancomycin and against E. faecium strains resistant to both aminoglycosides and clinically used pMactams, but also to fastidious Gram negative strains such as H.influenzae and Mxatarrhalis. Accordingly the present invention provides a compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, wherein HET is an N-linked 5-membered heteroaiyl ring, containing either (i) 1 to 3 further nitrogen heteroatoms or (ii) a further heteroatom selected from O and S together with an optional further nitrogen heteroatom; which ring is optionally substituted on a C atom by an oxo or thioxo group; and/or the ring is optionally substituted on a C atom by 1 or 2 (l-4C)alkyl groups; and/or on an available nitrogen atom (provided that the ring is not thereby quaternised) by (l-4C)aIkyl; or HET is an N-linked 6-membered heteroaryl ring containing up to three nitrogen heteroatoms in total (including the linking heteroatom), which ring is substituted on a suitable C atom by oxo or thioxo and optionally substituted on any available C atom by 1 or 2 (l-4C)alkyl substituents; Q is selected from Ql to Q9 :- wherein R2 and R3 are independently hydrogen or fluoro; wherein A1 is carbon or nitrogen; B1 is 0 or S (or, in Q9 only, NH); Xq is 0, S or N-R1 (wherein R1 is hydrogen, (l-4C)alkyl or hydroxy-(l-4C)alkyl); and wherein in Q7 each A1 is independently selected from carbon or nitrogen, with amaxirnum of 2 nitrogen heteroatoms in the 6-membered ring, and Q7 is linked to T via any of the A1 atoms (when A1 is carbon), and linked in the 5-membered ring via the specified carbon atom, or via Al when A, is carbon; Q8 is linked to T via either of the specified carbon atoms in the 5- membered ring, and linked in the benzo-ring via either of the two specified carbon atoms on either side of the linking bond shown; and Q9 is linked via either of the two specified carbon atoms on either side of the linking bond shown; wherein T is selected from the groups in (TA) to (TD) below (wherein AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 are defined hereinbelow); (TA) T is selected from the following groups :- (TAa) AR1, ARl-(l-4C)alkyl-, AR2 (carbon linked), AR3; (TAb) ARl-CH(OH),AR2-CH(OH)-,AR3-CH(OH)s (TAc) AR1 -CO-, AR2-CO-, AR3-CO-, AR4-CO-; (TAd) AR1-0-, AR2-0-, AR3-0-; (TAe) AR1-S(0)q-, AR2-S(0)q-, AR3-S(0)q- (q is 0,1 or 2); (TAf) an optionally substituted N-linked (fully unsaturated) 5-membered heteroaryl ring system containing 1,2 or 3 nitrogen atoms; (TAg) a carbon linked tropol-3-one or tropol-4-one, optionally substituted in a position not adjacent to the linking position; or (TB) T is selected from the following groups :- (TBa) halo or (l-4C)alkyl {optionally substituted by one or more groups each independently selected from hydroxy, (1- 4C)alkoxy, (l-4C)alkanoyl, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, -NRvRw, (1- 6C)alkanoylamino, (l-4C)alkoxycarbonylamino, N-(l-4C)aIkyl-N-(l-6C)aUcanoylarnino, (1- 4C)alkylS(0)q- (q is 0,1 or 2), CY1, CY2 or AR1}; (TBb) -NRv'Rw1; (TBc) ethenyl, 2-(l-4C)alkylethenyL 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2- nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-((l-4C)alkylarninocarbonyl)ethenyl, 2-((l- 4C)allcoxycarbonyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl; (TBd) R10CO-, R10S(O)q- (q is 0,1 or 2) or RI0CS- wherein R10 is selected from the following groups :- (TBda) CYl or CY2; (TBdb) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw, ethenyl, 2-(l- 4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyl, 2-nitro-2- ((l-4C)alkyl)ethenyl, 2-((l-4C)alkylammocarbonyl)ethenyl, 2-((l- 4C)alkoxycarbonyl)etlienyl) 2-(ARl)ethenyl or 2-(AR2)ethenyl; or (TBdc) (l-4C)alkyl {optionally substituted as defined in (TBa) above, or by (1- 4C)alkylS(0)pNH- or (l-4C)alkylS(0)p.((l-4C)alkyl)N- (p is 1 or 2)}; wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl; Rv' is hydrogen, (1- 4C)alkyl or (3-8C)cycloalkyl; Rw1 is hydrogen, (l-4C)alkyi, (3-8C)cycloalkyl, (l-4C)alkyl- CO-or (l-4C)alkylS(0)q-(q is 1 or 2); or (TC) T is selected from the following groups :- (TCa) an optionally substituted, fully saturated 4-membered monocyclic ring containing 1 heteroatom selected from O, N and S (optionally oxidised), and linked via a ring nitrogen or sp3 carbon atom; (TCb) an optionally substituted 5-membered monocyclic ring containing 1 heteroatom selected from O, N and S (optionally oxidised), and linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom, which monocyclic ring is fully saturated other than (where appropriate) at a linking sp2 carbon atom; (TCc) an optionally substituted 6- or 7-membered monocyclic ring containing 1 or 2 heteroatoms independently selected from O, N and S (optionally oxidised), and linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom, which monocyclic ring is fully saturated other than (where appropriate) at a linking sp2 carbon atom; or (TD) T is selected from the following groups :- (TDa) a bicyclic spiro-ring system containing 0,1 or 2 ring nitrogen atoms as the only ring heteroatoms, the structure consisting of a 5- or 6-membered ring system (linked via a ring mtrogen atom or a ring sp3 or sp2 carbon atom) substituted (but not adjacent to the linking position) by a 3-, 4- or 5-membered spiro-carbon-linked ring; which bicyclic ring system is (i) fully saturated other than (where appropriate) at a linking sp2 carbon atom; (ii) contains one -N(Rc)- group in the ring system (at least two carbon atoms away from the linking position when the link is via a nitrogen atom or an sp2 carbon atom) or one -N(Rc)- group in an optional substituent (not adjacent to the linking position) and is (iii) optionally further substituted on an available ring carbon atom; or (TDb) a 7-, 8- or 9-membered bicyclic ring system (linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom) containing 0,1 or 2 ring nitrogen atoms (and optionally a further 0 or S ring heteroatom), the structure containing a bridge of 1, 2 or 3 carbon atoms; which bicyclic ring system is (i) fully saturated other than (where appropriate) at a linking sp2 carbon atom; (ii) contains one O or S heteroatom, or one -N(Rc)- group in the ring (at least two carbon atoms away from the linking position when the link is via a nitrogen atom or an sp2 carbon atom) or one -N(Rc)- group in an. optional substituent (not adjacent to the linking position) and is (iii) optionally further substituted on an available ring carbon atom; wherein Re is selected from groups (Rcl) to (Rc5) :- (Rcl) (l-6C)alkyl {optionally substituted by one or more (l-4C)alkanoyl groups (including geminal disubstitution) and/or optionally monosubstituted by cyano, (l-4C)alkoxy, trifluoromethyl, (l-4C)alkoxycarbonyl, phenyl (optionally substituted as for AR defined hereinafter), (l-4C)alkylS(0)q- (q is 0,1 or 2); or, on any but the first carbon atom of the (1-6C)alkyl chain, optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy and fluoro, and/or optionally monosubstituted by oxo, -NRvRfy [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], (l-6C)alkanoylamino, (l-4C)antoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylamino, (l-4C)aIkylS(0)pNH- or (l-4C)alkylS(0)p-((l-4C)alkyl)N- (p is 1 or 2)}; (Rc2) R13CO- , R13S02- or Rl3CS-wherein R13 is selected from (Rc2a) to (Rc2e) :- (Rc2a) AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1, CY2; (Rc2b) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], ethenyl, 2-(l-4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)aJJcyi)ethenyl, 2-nitroethenyL 2-nitro-2-((l-4C)alkyI)ethenyL 2-((l-4C)alkylaminocarbonyl)ethenyl 2-((l-4C)alkoxycarbonyl)ethenyI, 2-(ARl)ethenyl, 2-(AR2)ethenyl, 2-(AR2a)ethenyl; (Rc2c) (l-lOC)alkyl {optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy, (l-lOC)alkoxy, (l-4C)alkoxy-(l-4C)alkoxy, (1-4C)aIkoxy-(l-4C)aIkoxy-(l-4C)alkoxy, (l-4C)aIkanoyl,phosphoryl [-0-P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphiryl [-0-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives thereof], and amino; and/or optionally substituted by one group selected from phosphonate [phosphono, -P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphinate [-P(OH), and mono- and di-(l-4C)alkoxy derivatives thereofj, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)aIkoxycarbonyl, (1 -4C)alkoxy-(l -4C)allcoxy-(l -4C)alkoxycarbonyl, (1 -4C)aUcylarnino, di((l-4C)all£yl)amino, (l-6C)aUcanoylamino, (l-4C)alkoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylamino, (l-4C)alkylaminocarbonyl, di((l-4C)alkyl)aminocarbonyl, (1-4C)alkylS(0)pNH-, (l-4C)alkylS(0)p-((l-4C)alkyl)N-, fluoro(l-4C)allcylS(0)pNH-, fluoro(l-4C)alkylS(0)p((l-4C)allcyl)N-, (l-4C)alkylS(0)q- [the (l-4C)alkyl group of (1-4C)alkylS(0)q- being optionally substituted by one substituent selected from hydroxy, (1-4C)alkoxy, (l-4C)allcanoyl, phosphoryl [-0-P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphiryl [-0-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives thereofj, amino, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxycarbonyl, carboxy, (1-4C)altylamino, di((l^C)alkyl)amino, (l-6C)alkanoylamino, (l-4C)alkoxycarbonylarnino, N-(l-4C)aUcyl-N-(l-6C)aIkanoylamino, (l-4C)alkylaminocarbonyl} di((l-4C)alkyl)aminocarbonyl, (l-4C)alkylS(0)pNH-, (l-4C)alkylS(0)p-((l-4C)alkyl)N-, (1-4C)alkylS(0)q-, AR1-S(0)q-, AR2-S(0)q-, AR3^S(0)q- and also AR2a, AR2b, AR3a and AR3b versions of AR2 and AR3 containing groups], CY1, CY2, AR1, AR2, AR3, AR1-0-, AR2-0-, AR3-0-, AR1-S(0)q-, AR2-S(0)q-, AR3-S(0)q-, AR1-NH-, AR2-NH-, AR3-NH-(p is 1 or 2 and q is 0,1 or 2), and also AR2a, AR2b, AR3a and APv3b versions of AR2 and AR3 containing groups}; (Rc2d) R14C(0)0(l-6C)alkyl wherein R14is AR1, AR2, (l-4C)alkylamino (the (1- 4C)alkyl group being optionally substituted by (l-4C)alkoxycarbonyl or by carboxy), benzyloxy-(l-4C)alkyl or (l-10C)alkyl {optionally substituted as defined for (Rc2c)}; (Rc2e) R150- wherein R15 is benzyl, (l-6C)alkyl {optionally substituted as defined for (Rc2c)}5 CY1, CY2 or AR2b; (Rc3) hydrogen, cyano, 2-cyanoelhenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-((l-4C)all^laminocarbonyl)ethenyl, 2-((l-4C)alkoxycarbonyl)ethenyL 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl, or of the formula (Rc3a) (Rc3a) wherein X00 is -OR17, -SR17, -NHR17and -N(R17)2; i wherein R17 is hydrogen (when X00 is -NHR,7and -N(R17)2), and R17 is (l-4C)alkyl, phenyl or AR2 (when X00 is -OR17, -SR17 and -NHR17); and R,e is cyano, nitro, (l-4C)alkylsulfonyl, (4-7C)cycloalkylsulfonyl, phenylsulfonyl, (l-4C)alkanoyl and (l-4C)alkoxycarbonyl; (Rc4) trityl,ARl,AR2,AR2a,AR2b,AR3,AR3a,AR3b; (Rc5) RdOC(Re)=CH(C=0)-, RfC(O)C(=0)-, RgN=C(Rh)C(=0)- or RiNHC(Rj)=CHC(=0)- wherein Rd is (l-6C)alkyl; Re is hydrogen or (l-6C)alkyl, or Rd and Re together form a (3-4C)alkylene chain; Rf is hydrogen, (l-6C)alkyl, hydroxy(l-6C)alkyl, (l-6C)alkoxy(l-6C)alkyl, -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], (l-6C)alkoxy, (l-6C)allcoxy(l-6C)alkoxy, hydroxy(2-6C)allcoxy, (1-4C)aUcylamino(2-6C)alkoxy1 di-(l-4C)a!kylammo(2-6C)an!:oxy; Rg is (l-6C)alkyl, hydroxy or (l-6C)aUcoxy; Rh is hydrogen or (l-6C)alkyl; Ri is hydrogen, (l-6C)alkyl, AR1, AR2, AR2a, AR2b and Rj is hydrogen or (l-6C)alkyl; wherein AR1 is an optionally substituted phenyl or optionally substituted naphthyl; AR2 is an optionally substituted 5- or 6-membered, fully unsaturated (i.e with the maximum degree of unsaturation) monocyclic heteroaryl ring containing up to four heteroatoms independently selected from O, N and S (but not containing any O-O, 0-S or S-S bonds), and linked via a ring carbon atom, or a ring nitrogen atom if the ring is not thereby quaternised; AR2a is a partially hydrogenated version of AR2 (i.e. AR2 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom or linked via a ring nitrogen itom if the ring is not thereby quatemised; AR2b is a fully hydrogenated version of AR2 (i.e. AR2 systems having no unsaturation), linked via a ring carbon atom or linked via a ring nitrogen atom; AB3 is an optionally substituted 8-, 9- or 10-membered, fully unsaturated (i.e with the maximum degree of unsaturation) bicyclic heteroaryl ring containing up to four heteroatoms independently selected from O, N and S (but not containing any O-O, 0-S or S-S bonds), and linked via a ring carbon atom in either of the rings comprising the bicyclic system; AR3a is a partially hydrogenated version of AR3 (i.e. AR3 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom if the ring is not thereby quatemised, in either of the rings comprising the bicyclic system; AR3b is a rally hydrogenated version of AR3 (i.e. AR3 systems having no unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom, in either of the rings comprising the bicyclic system; AR4 is an optionally substituted 13- or 14-membered, fully unsaturated (i.e with the maximum degree of unsaturation) tricyclic heteroaryl ring containing up to four heteroatoms independently selected from 0, N and S (but not containing any 0-0, 0-S or S-S bonds), and linked via a ring carbon atom in any of the rings comprising the tricyclic system; AR4a is a partially hydrogenated version of AR4 (i.e. AR4 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom if the ring is not thereby quatemised, in any of the rings comprising the tricyclic system; CY1 is an optionally substituted cyclobutyl, cyclopentyl or cyclohexyl ring; CY2 is an optionally substituted cyclopentenyl or cyclohexenyl ring. In this specification, where it is stated that a ring may be linked via an sp2 carbon atom, which ring is fully saturated other than (where appropriate) at a linking sp2 carbon atom, it is to be understood that the ring is linked via one of the carbon atoms in a C=C double bond. In another embodiment, (Rcl) is as defined above other than the optional phenyl substituent on (l-6C)alkyl is optionally substituted as for AR1 defined hereinafter; and (Rc2c), is as defined above and further includes carboxy as an optional substituent on R13 as (l-lOC)alkyl. (TAf) When T is an optionally substituted N-linked (fully unsaturated) 5-membered heteroaryl ring system containing 1,2 or 3 nitrogen atoms, it is preferably selected from a group of formula (TAfl) to (TAf6) below (particularly (TAfl), (TA£2), (TAf4) and (TAf5), and especially (TAfl) and/or (TA£2)). The above preferred values of (TAf) are particularly preferred when present in Ql or Q2, especially Ql. (TAf4) (TAfS) (TAf6) wherein: R6 is selected (independently where appropriate) from hydrogen, (l-4C)alkyl, (1- 4C)alkoxycarbonyl, (l-4C)alkanoyl, carbamoyl and cyano; R4 and R5 are independently selected from hydrogen, halo, trifluoromethyl, cyano, nitro, (1- 4C)alkoxy, (l-4C)alkylS(0)q- (q is 0,1 or 2), (l-4C)alkanoyl, (l-4C)alkoxycarbonyl, (2- 4C)alkanoyloxy-(l-4C)alkyL benzoxy-(l-4C)alkyl, (2-4C)allcanoylamino, -CONRvRw, - NRvRw and (l-4C)alkyl {optionally substituted by hydroxy, trifluoromethyl, cyano, nitro, (1- 4C)alkoxy, (l-4C)alkylS(0)q- (qis 0,1 or 2), (l-4C)allcoxycarbonyl, (MC)alkanoylamino; -CONRvRw, -NRvRw; wherein RvRw is hydrogen or (l-4C)aIkyl; Rw is hydrogen or (1- 4C)alkyl}; or R4 is selected from one of the groups in (TAfa) to (TAfc) below, or (where appropriate) one of R4 and R5 is selected from the above list of R4 and R5 values, and the other is selected from one of the groups in (TAfa) to (TAfc) below :-(TAfa) a group of the formula (TAfal) wherein Z° is hydrogen or (l-4C)alkyl; X° and Y° are independently selected from hydrogen, (l-4C)alkyl, (l-4C)alkoxycarbonyl, halo, cyano, nitro, (l-4C)alkylS(0)q- (q is 0,1 or 2), RvRwNS02-, trifluoromethyl, pentafluoroethyl, (l-4C)alkanoyl and -CONRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl]; or one of X° and Y° is selected from the above list of X° and Y° values, and the other is selected from phenyl, phenylcarbonyL, -S(0)q-phenyl (q is 0,1 or 2), H- (phenyl)carbamoyl, phenylaminosulfonyl, AR2, (AR2)-CO-, (AR2)-S(0)q- (q is 0,1 or 2), N-(AR2)carbamoyl and (AR2)aminosulfonyl; wherein any phenyl group in (TAfa) may be optionally substituted by up to three substituents independently selected from (l-4C)alkyl, cyano, trifluoromethyl, nitro, halo and (l-4C)alkylsulfonyl; (TAfb) an acetylene of the formula -=-H or -=-(l-4C)alkyl; (TAfc) -X1-Y,-AR2, -X'-Y'-ARZa, -X'-Y,-AR2b, -X'-Y'-ARS, -X'-Y'-ARSa or -X'-Y1- AR3b; wherein X1 is a direct bond or -CH(OH)- and Y1 is -(CH^-, -(CH2)n-NH-(CH2)m-, -C0-(CH2)m-, -CONH-(CH2)m-, -C(=S)NH-(CH2)m- or - C(O)0-(CH2)m-; or wherein X1 is -(CH2)n- or -CH.(M.€)-(CE^m- and Y1 is -(CH^-NH^CH^-, -CO-(CH2)m-, -CONH-fCH^-, -C(=S)NH-(CH2)m-, -CKOCMCH^- or -S(0)q-(CH2)M-; or wherein X1 is -CH20, -CH2NH- or -OS2N((l-4C)aliyl)- and Y1 is -CO-(CH2)M- -CONH-(CH2)m- or -C(=S)NB-(CH2)m- ; and additionally Y1 is -S02- when X1 is -CH2NH- or -CH2N((l-4C)alkyl)-, and Y1 is -(CH2)M- when X1 is -CH20- or -CH2N((l-4C)alkyl)-; wherein n is 1,2 or 3; m is 0,1,2 or 3 and q is 0,1 or 2; and when Y1. is -(CH2)m-NH-(CH2)m- each m is independently selected from 0, 1, 2 or 3. It is to be understood that when a value for -X1- is a two-atom link and is written, for example, as -CH2NH- it is the left hand part (-CH2- here) which is bonded to the group of formula (TAfl) to (TAf6) and the right hand part (-NH- here) which is bonded to -Y1- in the definition in (TAfc). Similarly, when -Y1- is a two-atom link and is written, for example, as -CONH- it is the left hand part of -Y1- (-CO- here) which is bonded to the right hand part of-X1-, and the right hand part of-Y1- (-NH- here) which is bonded to the AR2, AR2a, AR2b, AR3, AR3a or AR3b moiety in the definition in (TAfc). Preferably R6 is hydrogen or (l-4C)alkyl, and R4 and R5 are independently selected from hydrogen, (l-4C)alkyl or one of R4 and R5 is selected from group (TAfa). Other preferable substituents on the (TAfl) to (TAf6) are illustrated in the accompanying Examples. Most preferable is (TAf2) with such preferable substituents. (TAg) When T is a carbon linked tropol-3-one or tropol-4-one, optionally substituted in a position not adjacent to the linkitig position (TAg), it is preferably selected from a group of formula (TAgl), (TAg2) or (TAg3). The above preferred values of (TAg) are particularly preferred when present in Ql or QJ2, especially Ql. 0 R7 (TAgl) (TAg2) (TAg3) wherein R7 is selected from (TAga)hydrogen, (l-4C)alkyl {optionally substituted by one or two substituents (excluding geminal ^'substitution) independently selected from fluoro, hydroxy, (I-4C)aIfcoxy and - • NRvRw]}; or (TAgb)RE-0-, R8-S-, R8-NH- or R.8R8-N-; wherein R8 is selected (independently where appropriate) from hydrogen, (l-4C)alkyl or (3- 8C)cycloalkyl {both optionally substituted by one or two substituents (excluding geminal disubstitution) independently selected from hydroxy, (l-4C)alkoxy, (l-4C)alkoxycarbonyl and -NRvRw}, (2-4C)alkenyl {optionally substituted by one or two -NRvRw substituents}, (1 -4C)alkanoyl {optionally substituted by one or two substituents independently selected from -NRvRw and hydroxy}, phenyl-(l-4C)alkyl or pyridyl-(l-4C)alkyl {the phenyl and pyridyl (preferably pyridin-4-yl) rings being optionally substituted by one or two -NRvRw substituents}; or (T^g^morpholino, thiomorpholino, pyrrolidino {optionally independently substituted in the 3- and/or 4-positions by (l-4C)alkyl}, piperidino substituted in the 4-position by R9-, R9-0-, R9-S-, R9~NH- or R^'-N-; wherein R9 is selected (independently where appropriate) from hydrogen, (l-4C)alkyl {optionally substituted by one or two (excluding geminal disubstitution) hydroxy, (l-4C)alkoxy, (l-4C)alkoxycarbonyl or-NRvRw} and piperazino {optionally substituted in the 4-position by (l-4C)alkyl, (3-8C)cycloallcyl, (l-4C)allcanoyl, (l-4C)alkoxycarbonyl or (l-4C)aIkylsulfonyl, and optionally independently substituted in the 3- and/or 5-positions by (l-4C)alkyl}; wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl. (TC) Preferred values for the optional substituents and groups defined in (TCa) to (TCc) are defined by formulae (TCI) to (TC4) :- (TCI) (TC2) (TC3) (TC4) wherein in (TCI): >A3-B3- is >C(Rq)-CH(Rr)- and G is -Q-, -S-, -SO-, -S02- or >N(Rc); wherein in (TC2) : ml is 0,1 or 2; >A3-B3- is >C=C(Rr)- or >C(Rq)-CH(Rr)- and G is -0-, -S-, -SO-, -SO,- or >N(Rc); wherein in (TC3): ml is 0,1 or 2; >A3-B3- is >C(Rq)-CH(Rr)- (other than when Rq and Rr are both together hydrogen) and G is -0-, -S-, -SO-, -S02- or >N(Rc); wherein in (TC4): nl is 1 or 2; ol is 1 or 2 and nl + ol = 2 or 3; >A3-B3- is >C=C(Rr)- or >C(Rq)-CH(Rr)- or >N-CH2- and G is -0-, -S-, -SO-, -S02- or >N(Rc); Rp is hydrogen, (1- 4C)aIkyl (other than when such substitution is defined by >A3-B3-), hydroxy, (l-4C)alkoxy or (l-4C)aLkanoyloxy; wherein in (TCI), (TC2) and (TC4); ml, nl and ol are as defined hereinbefore: >A3-B3- is >N-CHr and G is >C(R")(R12), >C=0, >C-OH, >C-(l-4C)alkoxy, >C=N-OH, >C=N-(l-4C)alkoxy, >C=N-NH-(l-4C)alkyl, >C=N-N((l-4C)alkyl)2 (the last two (1- 4C)alkyl groups above in G being optionally substituted by hydroxy) or >C=N-N-CO-(l- 4C)allcoxy; wherein > represents two single bonds; Rqis hydrogen, hydroxy, halo, (l-4C)alkyl or (l-4C)alkanoyloxy; Rr is (independently where appropriate) hydrogen or (l-4C)alkyl; R" is hydrogen, (l-4C)alkyl, fluoro(l-4C)aIkyl, (l-4C)allcyl-thio-(l-4C)alkyl or hydroxy-(l- 4C)alkyl and R12 is -[C(Rr)(Rr)]^-N(Rr)(Rc) wherein m2 is 0,1 or 2; and, other than the ring substitution defined by G, >A3-B3- and Rp, each ring system may be optionally further substituted on a carbon atom not adjacent to the link at >A3- by up to two substituents independently selected from (l~4C)alkyl, fluoro(l-4C)alkyl (including trifluoromethyl), (l-4C)alkyl-thio-(l-4C)alkyl, hydroxy-(l-4C)alkyl, amino, amino-(l- 4C)alxyl, (l^C)alkanoylamino, (l-4C)alkanoylamino-(l-4C)alkyl, carboxy, (1- 4C)alkoxycarbonyl, AR-oxymethyl, AR-thiomethyl, oxo (=0) (other than when G is >N-Rc and Re is group (Rc2) defined hereinbefore) or independently selected from Re; and also hydroxy or halo (the last two optional substituents only when G is -0- or -S-); wherein AR (or ARp) is as defined for formula (IP) hereinafter; Re is selected from groups (Rcl) to (Rc5) defined hereinbefore. For the avoidance of doubt, ( )rai, ( )ni and ()0l indicate (-CH2-)mi, (-CH2-)„i and (-CH,-)0l respectively (optionally substituted as described above). In the above definition of (TCI) to (TC4) and of the further optional substituents, AR is preferably AR2, and the further optional substituents are preferably not selected from the values listed for Re. A preferred value for G is >N(Rc) or >C(Rn)(R12). Particularly preferred values for the optional substituents and groups defined in (TCa) to (TCc), and (TCI) to (TC4) are contained in the following definitions (TC5) to (TCI 1):- (TC5) (TC6) (TC7) wherein Rc has any of the values listed hereinbefore or hereinafter. Especially preferred are (TC5), (TC6), (TC7) and (TC9), most especially (TC5) in which Re has any of the values listed hereinbefore or hereinafter (especially R13CO- with the preferable R13 values given hereinafter). In (TC5) Rc is preferably selected from the group (Rc2), especially R13CO with the preferable R13 values given hereinafter. In (TC7) Rc is preferably selected from group (Rc3) or (Rc4). The above preferred values of (TCa) to (TCc) are particularly preferred when present in Ql or Q2, especially Ql (especially when HET is isoxazole). (TDa) When T is a bicyclic spiro-ring system as defined in (TDa), it is preferably selected from a group of formula (TDal) to (TDa9). The above preferred values of (TDa) are particularly preferred when present in Ql or Q2, especially Ql. wherein; (i) the A4 linking group is a nitrogen atom or an sp3 or sp2 carbon atom (with the double bond, where appropriate, orientated in either direction); and (ii) one of the ring carbon atoms at positions marked * and ** is replaced by one of the following groups -NRc-, >CH-NHRc, >CH~NRc-(l-4C)alkyl, >CH-CH2-NHRc, >CH-CH2- NRc-(l-4C)alkyl [wherein a central -CH2- chain link is optionally mono- or di-substituted by (l-4C)alkyl]; with the provisos that positions marked * are not replaced by -NH- in the ring containing the A, link when A4 is a nitrogen atom or an sp2 carbon atom, and that positions . marked * are not replaced by -NH- in the three membered ring in (TDal), (TDa4) and (TDa5); and (iii) the ring system is optionally (further) substituted on an available ring carbon atom by up to two substituents independently selected from (l-4C)alkyl, fluoro(l-4C)aIkyl (including trifluoromethyl), (l-4C)aIkyl-thio-(l-4C)aIkyl, hydroxy-(l-4C)alkyl, amino, amino-(l- 4C)alkyl, (l-4C)a!kanoylamino,, (l-4C)alkanoylarnino-(l-4C)alkyl, cafboxy, (1- 4C)alkoxycarbonyl, AR2-oxymethyl, AR2-thiomethyl, oxo (=0) (other than when the ring contains an >N-Rc and Re is group (Rc2)) and also hydroxy or halo; wherein Re has any of the values listed hereinbefore or hereinafter. (TDb) When T is a 7-, 8- or 9-membered bicyclic ring system containing a bridge of 1, 2 or 3 carbon atoms as defined in (TDb), it is preferably selected from a group defined by the ring skeletons shown in formulae (TDbl) to (TDb 14) :- wherein; (i) the ring system contains 0,1 or 2 ring nitrogen atoms (and optionally a further O or S ring heteroatom),and when present the ring nitrogen, O or S heteroatom/s are at any position other than as part of the 3-membered ring in (TDbl); (ii) the ring system is linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom (with the double bond, where appropriate, orientated in either direction) from any position in either ring [other than from a bridgehead position or from an sp2 carbon atom in the 4- membered ring in (TDb2), (TDb6) and (TDbl 1)]; (iii) one of the ring carbon atoms at a position not adjacent to the linking position, is replaced (other than when the ring contains an 0 or S heteroatom) by one of the following groups -NR.c- [not at a bridgehead position], >C(H)-NHRc, >C(H)-NRc-(l-4C)alkyl, >C(H)-CH2-NHRc, >C(H)-CH2-NRc-(l-4C)alkyl [wherein the hydrogen atom shown in brackets is not present when the replacement is made at a bridgehead position and wherein a central -CH2- chain link is optionally mono- or di-substituted by (l-4C)alkylJ; with the proviso that when the ring system is linked via a ring nitrogen atom or an sp2 carbon atom any replacement of a ring carbon atom by -NRc-, 0 or S is at least two carbon atoms away from the linking position; and (iv) the ring system is optionally (further) substituted on an available ring carbon atom as for the bicyclic spiro-ring systems described in (TDa); wherein Re has any of the values listed hereinbefore or hereinafter. It will be appreciated that unstable anti-Bredt compounds are not contemplated in this definition (i.e. compounds with stuctures (TDb3), (TDb4), (TDb7), (XDb8), (TDb9), (TDM2), (TDbl3) and (TDbl4) in which an sp2 carbon atom is directed towards a bridgehead position). Particularly preferred values of (TDb) are the following structures of formula (TDb4), (TDb8) and/or (TDb9); wherein Re has any of the values listed hereinbefore or hereinafter. The above preferred values of (TDb) are particularly preferred when present in Ql or Q2, In another embodiment there is provided a compound of formula (3) as defined by formula (IP) below: especially Ql. wherein HET is an N-linked 5-membered heteroaryl ring, containing either (i) 1 to 3 farther nitrogen heteroatoms or (ii) a further heteroatom selected from O and S together with an optional further nitrogen heteroatom; which ring is optionally substituted on a C atom by an oxo or thioxo group; and/or the ring is optionally substituted on a C atom by 1 or 2 (l-4C)alkyl groups; and/or on an available nitrogen atom (provided that the ring is not thereby quaternised) by (l-4C)aUcyl; Qis wherein: R2 and R3 are independently hydrogen or fluoro; R6p is hydrogen, (1^4C)alkylJ hydroxy, (l-4C)alkoxy or (2-4C)alkanoyloxy; >A-B- is of the formula >OC(Ra)- , >CHCHRa-, >C(OH)CHRa- or >N-CH2- (> represents two single bonds) wherein Ra is hydrogen or (1 -4C)alkyl; DisO,S,SO, S02orNR7p; R4p and R5p are independently oxo (=0) [but not when R7p is group (PC) below], (l-4C)allcylJ (l-4C)alkanoylamino-(l-4C)alkyl, hydroxy-(l-4C)alkyl, carboxy, (l-4C)alkoxycarbonyl, ARp-oxymethyl, ARp-thiomethyl (wherein ARp is as defined hereinbelow) or independently as defined for R7p hereinbelow with the proviso that R4p and RSp are not phenyl, benzyl, ARp (as defined hereinbelow), a tetraaole ring system, cyclopentyl or cyclohexyl; and when D is 0 or S, R4p and Rsp are additionally independently hydroxy or bromo; wherein R7p is selected from (PA) to (PE) :- (PA) hydrogen, cyano, 2-((l-4C)alkoxycarbonyl)ethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-((1^4C)aIkylammocarbonyl)ethenyl; . (PB) phenyl, benzyl, ARp (as defined hereinbelow) or a tetrazole ring system [optionally mono-substituted in the 1- or 2- position of the tetrazole ring by (l-4C)alkyl, (2-4C)allcenyl, (2-4C)alkynyl or (l-4C)alkanoyl] wherein the tetrazole ring system is joined to the nitrogen in NR7p by a ring carbon atom; (PC) R1CpCO-,R10pSO2-orR10pCS- wherein R10p is selected from (PCa) to (PCf) :- (PCa) ARp (as defined hereinbelow); (PCb) cyclopentyl or cyclohexyl or l,3-dioxolan-4-yl or l,4-dioxan-2-yl or l,3-dioxan"4-yl [optionally mono- or disubstituted by substituents independently selected from (l-4C)alkyl (including geminal disubstitution), hydroxy (but excluding l,3-dioxolan-4-yl, l,4-dioxan-2-yl and l,3-dioxan-4-yl substituted by hydroxy), (l-4C)alkoxy, (l-4C)alkylthio, acetamido, (l-4C)alkanoyl, cyano and trifluoromethyl]; (PCc) hydrogen, (l«4C)alkoxycarbonyl, trifluoromethyl, amino, (l-4C)aU di((l-4C)altyl)arriino, 2-(5- or 6-membered heteroaryl)ethenyl, 2-(5- or 6-membered (partially) hydrogenated heteroaryl)ethenyl, 2-phenylethenyl [wherein the heteroaryl or phenyl substituent is optionally substituted on an available carbon atom by up to three substituents independently selected from (l-4C)alkoxy, halo, cyano and (for the phenyl substituent only) (l-4C)alkylsulfonylj; (PCd) (l-10C)aIkyl [optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy and amino, or optionally monosubstituted by cyano, halo, (MOQalkoxy, trifluoromethyl, (l-4C)alkoxy-(l-4C)alkoxy, (l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxy,(l-4C)aUcanoyl,(l-4C)alkoxycarbonyl, (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-6C0alkanoylamino, (l-4C)aIkoxycarbonylamino, HKl-4C)allkyl-N-(2-6C)alkanoylarnino, (l-4C)alkylS(0)pNH-, (l-4C)alkylS(0)p((l-4C)alkyl)N-, fluoro(l-4C)alkylS(0)pNH-, fluoro(l-4C)alkylS(0)p((l-4C)alkyl)N-,phosphono, (l-4C)alkoxy(hydroxy)phosphoryl, di-(l-4C)alkoxyphosphoryl, (l-4C)alkylS(0)q-, phenyl, naphthyl, phenoxy, naphthoxy, phenylamino, naphmylamino, phenylS(0)q-, naphthylS(0)q- [wherein said phenyl and naphthyl groups are optionally substituted by up to three substituents independently selected from (l-4C)alkoxy, halo and cyano], or CYp (as defined hereinbelow), wherein (where appropriate) p is 1 or 2 and q is 0,1 or 2]; (PCe) RUpC(0)0(l-6C)alkyl wherein Rup is an optionally substituted 5- or 6-membered heteroaryl, optionally substituted phenyl, (l-4C)a!kylamino, benzyloxy-(l-4C)alkyl or optionally substituted (l-10C)alkyl; (PCI) R12pO- wherein R12 p is benzyl or optionally substituted (1 -6C)alkyl; (PD) RdOC(Re)=€H(C=0)-, RfC(=0)C(=0)-, REN==C(Rh)C(=0)- or RiNHC(Rj)=CHC(==0)- wherein Rd is (l-6C)aIkyl, Re is hydrogen or (l-6C)alkyl, or Rd and Re together form a (3-4C)alkylene chain, Rfis hydrogen, (l-6C)aIkyl, hydroxy(l-6C)alkyl, (l-6C)alkoxy(l-6C)alkyl, amino, (l-4C)alkylamino, di-(l-4C)alkylarnino, (l-6C)alkoxy, (l-6C)alkoxy(l-6C)alkoxy, hydroxy(2-6C)alkoxy, (l-4C)alkylammo(2~6C)alkoxy, mXl-4C)alkylamino(2-6C)a]koxy, Rg is (l-6C)alkyl, hydroxy or (l-6C)alkoxy, Rh is hydrogen or (l-6C)aIkyl, R is hydrogen, (l-6C)alkyl, optionally substituted phenyl or an optionally substituted 5- or 6-membered heteroaryl [and (partially) hydrogenated versions thereof] and RJ is hydrogen or (l-6Qalkyl; (PE) R14PCH(R13P)(CH2)M wherein m is 0 or 1, R13p is fluoro, cyano, (l-4C)alkoxy, (l-4C)alkylsulfonyl, (l-4C)alkoxycarbonyl or hydroxy, (provided that when m is 0, RI3p is not fluoro or hydroxy) and R,4p is hydrogen or (l-4C)alkyl; wherein ARp is optionally substituted phenyl, optionally substituted phenyl(l-4C)alkyl, optionally substituted naphthyl, optionally substituted 5- or 6-membered heteroaryl; wherein ARp is also an optionally substituted 5/6 or 6/6 bicyclic heteroaryl ring system, in which the bicyclic heteroaryl ring systems may be linked via an atom in either of the rings comprising the bicyclic system, and wherein botii the mono- and bicyclic heteroaryl ring systems are linked via a ring carbon atom and may be (partially) hydrogenated; wherein CYp is selected from:- (i) 4-, 5- or 6-membered cycloalkyl ring; (ii) 5- or 6-membered cycloalkenyl ring; (iii) 5- or 6-membered heteroaryl, 5- or 6-membered heteroaryloxy, 5- or 6-membered heteroaryl-S(0)q-, 5- or 6-membered heteroarylamino [and (partially) hydrogenated versions thereof] and (iv) 5/6 or 6/6 bicychc heteroaryl, 5/6 or 6/6 bicyclic heteroaryloxy, 5/6 or 6/6 bicychc heteroaryl-S(0)q-, 5/6 or 6/6 bicychc heteroarylarnino [and (partially) hydrogenated versions thereof]; wherein q is 0,1 or 2 and any of the aforementioned ring systems in CYp may be optionally substituted by up to three substituents independently selected from halo, (l-4C)alkyl [including geminal disubstitution when CYp is a cycloalkyl or cycloalkenyl ring], acyl, oxo andnitro-(l-4C)alkyl; and pharmaceutically-acceptable salts thereof. In this embodiment (IP) of the specification the term 'alkyl' includes straight chained and branched structures. For example,' (l-6C)alkyI includes propyl, isopropyl and tert-butyl. However, references to individual alkyl groups such as "propyl" are specific for the straight chained version only, and references to individual branched chain alkyl groups such as "isopropyl" are specific for the branched chain version only. A similar convention applies to other radicals, for example halo(l-4C)alkyl includes 1-bromoethyl and 2-bromoethyl. In this embodiment (IP) of the specification a '5- or 6-membered heteroaryl' and 'heteroaryl (monocyclic) ring' means a 5- or 6-membered aryl ring wherein (unless stated otherwise) 1,2 or 3 of the ring atoms are selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5- or 6-membered heteroaryl ring systems are furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole and thiophene. In this embodiment (IP) of the specification a l5/6 or 6/6 bicychc heteroaryl ring system' and 'heteroaryl (bicychc) ring' means an aromatic bicychc ring system comprising a 6-membered ring fused to either a 5 membered ring or another 6 membered ring, the bicychc ring system containing 1 to 4 heteroatoms selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5/6 and 6/6 bicychc ring systems are indole, benzofuran, benzoimidazole, benzothiophene, benzisothiazole, benzoxazole, benzisoxazole, pyridoimidazole, pyrimidoimidazole, quinoline, quinoxaline, quinazoline, phthalazine, cinnoline and naphthyridine. In this embodiment (IP) of the specification a '4-, 5- or 6-membered cycloalkyl ring' means a cyclobutyl, cyclopentyl or cyclohexyl ring; and a '5- or 6-membered cycloalkenyl ring' a means cyclopentenyl or cyclohexenyl ring. Particular optional substituents for alkyl, phenyl (and phenyl containing moieties) and naphthyl groups and ring carbon atoms in heteroaryl (mono or bicyclic) rings in Rllp, RI2p, R and ARp include halo, (l-4C)alkyl, hydroxy, nitro, carbamoyl, (l-4C)alkylcarbamoyl, di-((l-4C)alkyl)carbamoyl, cyano, trifluoromethyl, trifluoromethoxy, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-4C)alkylS(0)q-, (wherein q is 0,1 or 2), carboxy, (l-4Qalkoxycarbony}, (2-4C)alkenyl, (2-4C)alkynyl, (l-4C)aJkmoyl, (l-4C)alkoxy, (l-4C)alkylS(0)2amino, (l-4C)alkanoylamino, benzoylamino, benzoyl, phenyl (optionally substituted by up to three substituents selected from halo, (l-4C)alkoxy or cyano), furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene, hydroxyimino(l-4C)alkyl, (l-4C)alkoxyimmo(l-4C)alkyl, hydroxy-(l-4C)alkyl, halo-(l-4C)alkyl, nitro(l-4C)alkyl, amino(l-4C)aU bicyclic) rings in Rllp, R1 and ARp may be mono- or disubstituted on ring carbon atoms with substituents independently selected from the above list of particular optional substituents. For the avoidance of doubt, phosphono is -P(0)(OH)2; (l-4C)alkoxy(hydroxy)-phosphoryl is amono-(l-4C)aIkoxy derivative of -0-P(0)(OH)2; and di-(l-4C)alkoxyphosphoryl is a di-(l-4C)alkoxy derivative of-O-P(0)(OH)2. In this embodiment of formula (IP) a '5- or 6-membered heteroaryl' and 'heteroaryl (monocyclic) ring' means a 5- or 6-membered aryl ring wherein (unless stated otherwise) 1,2 or 3 of the ring atoms are selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5- or 6-membered heteroaryl ring systems are furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole and thiophene. Particular examples of 5-membered heteroaryl rings containing 2 or 3 heteroatoms independently selected from N, 0 and S (with the proviso that there are no O-O, 0-S or S-S bonds; and in an alternative embodiment, also no N-S bonds) are pyrazole, imidazole, 1,2,3-triazole, 1,2,4-triazole, oxazole, isoxazole, thiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole; and also in an alternative embodiment, isothiazole, 1,2,5-thiadiazole, 1,2,4-thiadiazole or 1,2,3-thiadiazole. In this embodiment of formula (IP) a '5/6 or 6/6 bicyclic heteroaryl ring system' and 'heteroaryl (bicychc) ring' means an aromatic bicyclic ring system comprising a 6-membered ring fused to either a 5 membered ring or another 6 membered ring, the bicyclic ring system containing 1 to 4 heteroatoms selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5/6 and 6/6 bicyclic ring systems arc indole, benzofiiran, benzhmdazole, benzothiopheiie, benzisothiazole, benzoxazole, benzisoxazole, pytidoimidazole, pyrimidoimidazole, quinoline, quinoxaline, quinazoline, phthalazine, cinnoline and naphthyridine. Particular optional substituents for alkyl, phenyl (and phenyl containing moieties) and naphthyl groups and ring carbon atoms in heteroaryl (mono or bicyclic) rings in R14p, R,5p, Ri and ARp include halo, (l-4C)alltyl, hydroxy, nitro, carbamoyl, (l-4C)alkylcarbamoyl, di-((l-4C)alkyl)carbamoyl, cyano, trifluoromethyl, trifluoromethoxy, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-4C)alkyl S(O) - (q is 0,1 or 2), carboxy, (l-4C)alkoxycarbonyl, (2- 4C)alkenyl, (2-4C)alkynyl, (l-4Qalkanoyl, (l-4C)alkoxy, (l-4C)alkylS(0)2amino, (1-4C)alkanoylarnino, benzoylamino, benzoyl, phenyl (optionally substituted by up to three substituents selected from halo, (l-4C)alkoxy or cyano), furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene, hydroxyirriino(l-4C)aIkyl, (MC)aUcoxyirnino(l-4C)alkyl, hydroxy-(l-4C)alkyl, halo-(l-4C)alkyl, nitro(l-4C)alkyl, amino(l-4C)alkyl, cyano(l-4C)alkyl, (l-4C)alkanesulfonamido, aminosulfonyl, (l-4C)alkylaminosulfonyl anddi-((l-4C)aHcyl)ammosulfonyl. The phenyl and naphthyl groups and heteroaryl (mono- or bicyclic) rings in R,4p, Ri and ARp may be mono- or di-substituted on ring carbon atoms with substituents independently selected from the above list of particular optional substituents. In this specification the term 'alkyl' includes straight chained and branched structures. For example, (l-6C)alkyl includes propyl, isopropyl and tert-butyl. However, references to individual alkyl groups such as "propyl" are specific for the straight chained version only, and references to individual branched chain alkyl groups such as "isopropyl" are specific for the branched chain version only. A similar convention applies to other radicals, for example halo(l-4C)alkyl includes 1-bromoethyl and 2-bromoethyl. There follow particular and suitable values for certain substituents and groups referred to in this specification. These values may be used where appropriate with any of the definitions and embodiments disclosed hereinbefore, or hereinafter. Examples of (l-4C)alkyl and (l-5C)alkyl include methyl, ethyl, propyl, isopropyl and t-butyl; examples of (l-6C)aIkyI include methyl, ethyl, propyl, isopropyl, t-butyl, pentyl and hexyl; examples of (l-lOC)alkyl include methyl, ethyl, propyl, isopropyl, pentyl, hexyl, heptyl, octyl andnonyl; examples of (l-4C)alkaiioyIamino-(l-4c) alkyl include formamidomethyl, acetamidomethyl and acetamidoethyl; examples of hydroxy(l-4C)alkyl and hydroxy(l-6C)aIkyI include hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl and 3-hydroxypropyl; examples of (l-4C)alkoxycarbonyl include methoxycarbonyl, ethoxycarbonyl and propoxycarbonyl; examples of 2-((l-4C)aIkoxycarbonyl)ethenyl include 2-(methoxycarbonyl)ethenyl and 2-(ethoxycarbonyl)ethenyl; examples of 2-cyano-2-((l-4C)alkyl)ethenyI include 2-cyano-2-methylethenyl and 2-cyano-2-ethylethenyl; examples of 2-nitro-2-((l-4C)aIkyl)ethenyl include 2-nitro-2-methylethenyl and 2-nitro-2-ethylethenyl; examples of 2-((l-4C)aIkylammocarbonyl)ethenyl include 2-(memylaminocarbonyl)ethenyl and2-(emylaminocarbonyl)ethenyl; examples of (2-4C)aIkenyI include allyl and vinyl; examples of (2-4C)aIkynyI include ethynyl and 2-propynyl; examples of (l-4C)aIkanoyl include formyl, acetyl and propionyl; examples of (1-4C)alkoxy include methoxy, ethoxy and propoxy; examples of (l-6C)aIkoxy and (1-lOQalkoxy include methoxy, ethoxy, propoxy and pentoxy; examples of (l-4C)aIkylthio include methylthio and ethylthio; examples of (l-4C)aIkylamino include methylamino, emylarnino and propylamino; examples of di-((l-4C)alkyl)amino include dimemylamino, N-ethyl-N-memylamino, diethylamino, N-memyl-N-propylamino and dipropylamino; examples of halo groups include fluoro, chloro andbromo; examples of (l-4C)alkylsulfonyl include methylsulfonyl and ethylsulfonyl; examples of (l-4C)allcoxy-(l-4Qalkoxy and (1-6C)alkoxy-(l-6C)aIkoxy include methoxymethoxy, 2-methoxyethoxy, 2-ethoxyethoxy and 3-methoxypropoxy; examples of (l»4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxy include 2-(methoxymethoxy)ethoxy, 2-(2-methoxyethoxy)ethoxy; 3-(2-methoxyethoxy)propoxy and 2-(2-ethoxyethoxy)ethoxy; examples of (l-4C)aIkyIS(0)2amino include methylsulfonylamino and ethylsulfonylamino; examples of (l-4C)alkanoylamino and (l-6C)aIkanoylamrao include formamido, acetamido andpropionylamino; examples of (l-4C)alkoxycarbonyIamino include memoxycarbonylamino and emoxycarbonylamino; examples of N-(l-4C)aIkyl-N-(l- oC)aiKanoyiamino include N-methylacetamido, N-ethylacetamido and N-methylpropionamido; examples of (l-4C)aIkylS(0)pNH- wherein p is 1 or 2 include memylsulfinylamino, methylsulfonylamino, emylsulfmylamino and ethylsulfonylamino; examples of (l-4C)alkylS(0)p((l-4C)aIkyl)N- wherein p is 1 or 2 include > melnylsulfinylmemylamino, memylsulfonylmethylamino, 2-(ethylsulfinyl)ethylamino and 2-(ethylsulfonyl)ethylamino; examples of fluoro(l-4C)aIkyIS(0)pNH- wherein p is 1 or 2 include trifluoromemylsulfmylamino and trifluoromethylsulfonylamino; examples of fluoro(l-4QaIkylS(0)p((l-4C)alkyI)NH- wherein p is 1 or 2 include trifluoromemylsuMnylmethylamino andtrifluoromemylsulfonylmemylamino examples of (1-4C)aIkoxy(hydroxy)phosphoryl include methoxy(hydroxy)phosphoryl and ethoxy(hydroxy)phosphoryl; examples of di-(l-4Qalkoxyphosphoryl include di-methoxyphosphoryl, di-ethoxyphosphoryl and ethoxy(methoxy)phosphoryl; examples of (1-4C)aIkylS(0)q- wherein q is 0,1 or 2 include methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl and ethylsulfonyl; examples of phenylS(0)q and naphthyIS(0)q- wherein q is 0, l or 2 are phenylthio, phenylsulflnyl, phenylsulfonyl and naphthylthio, naphthylsulBnyl and naphthylsulfonyl respectively; examples of benzyloxy-(l-4QalkyI include benzyloxymethyl and benzyloxyethyl; examples of a (3-4C)aIkyIene chain are trimethylene or tetramethylene; examples of (l-6C)alkoxy-(l-6C)alkyI include methoxymethyl, ethoxymethyl and 2-methoxyethyl; examples of hydroxy-(2-6C)aIkoxy include 2-hydroxyethoxy and 3-hydroxypropoxy; examples of (l-4C)aIkylamino-(2-6C)alkoxy include 2-methylaminoethoxy and 2-ethylaminoethoxy; examples of di-(l-4C)aIkylamino-(2-6C)aIkoxy include 2-dimethylaminoethoxy and 2-diemylaminoethoxy; examples of phenyI(l-4C)alkyl include benzyl and phenethyl; examples of (1-4C)alkylcarbamoyl include memylcarbamoyl and ethylcarbamoyl; examples of di((l-4QaIkyl)carbamoyI include di(methyl)carbamoyl and di(ethyl)carbamoyl; examples of nydroxyimino(l-4C)aIkyl include hydroxyiminomethyl, 2-(hydroxyimino)ethyl and 1-(hydroxyimino)ethyl; examples of (l-4Qalkoxyimino-(l-4C)alkyl include memoxyiminomethyl, emoxyiminomethyl, l-(methoxyimino)ethyl and 2-(memoxyimino)ethyl; examples of halo(l-4C)alkyl include, halomethyl, 1-haloethyl, 2-haloethyl, and 3-halopropyl; examples of nitro(l-4C)aIkyI include nitromethyl, 1-nitroethyl, 2-nitroethyl and 3-nitropropyl; examples of ammo(l-4C)alkyl include aminomethyl, 1- aminoethyl, 2-aminoethyl and 3~aminopropyl; examples of cyano(l-4C)alkyl include cyanomethyl, 1-cyanoethyl, 2-cyanoethyl and 3-cyanopropyl; examples of (1-4C)alkanesuIfonamido include methanesulfonamido and ethanesulfonamido; examples of (l-4C)alkylaininosuIfonyl include memylaminosulfonyl and emylarninosulfonyl; and examples of di-(l-4C)alkylaminosuIfonyl include dimemylaminosulfonyL diethylaminosulfonyl and N-methyl-N-ethylaminosulfonyl; examples of (1-4C)alkanesntfonyloxy include methylsulfonyloxy, ethylsulfonyloxy and propylsulfonyloxy; examples of (l-4C)alkanoyIoxy include acetoxy; examples of (l-4C)alkylaminocarbonyl include methylaminocarbonyl and ethylaminocarbonyl; examples of di((l-4C)alkyl)aminocarbonyl include dimemylaminocarbonyl and diemylaminocarbonyl; examples of (3-8C)cycIoalkyl include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl; examples of (4-7C)cycIoalkyl include cyclobutyl, cyclopentyl and cyclohexyl; examples of di(N-(l~4C)alkyl)aminomethylimino include dimethylarmnomethylimino and diethylammomemylimino. Particular values for AR2 include, for example, for those AR2 containing one heteroatom, furan, pyrrole, thiophene; for those AR2 containing one to four N atoms, pyrazole, imidazole, pyridine, pyrimidine, pyrazine, pyridazine, 1,2,3- & 1,2,4-triazole and tetrazole; for those AR2 containing one N and one O atom, oxazole, isoxazole and oxazine; for those AR2 containing one N and one S atom, tbiazole and isothiazole; for those AR2 containing two N atoms and one S atom, 1,2,4- and 1,3,4-thiadiazole. Particular examples of AR2a include, for example, dihydropyrrole (especially 2,5-dihydropyrrol-4-yl) and tetrahydropyridine (especially l,2,5,6-tetrahydropyrid-4-yl). Particular examples of AR2b include, for example, tetrahydrofuran, pyrrolidine, morpholine (preferably morpholino), thiomorpholine (preferably thiomorpholino), piperazine (preferably piperazmo), imidazoline and piperidine, l,3-dioxolan-4-yl, l,3-dioxan-4-yl, 1,3-dioxan-5-yl and l,4-dioxan-2-yl. Particular values for AR3 include, for example, bicyclic benzo-fused systems containing a 5- or 6-membered heteroaryl ring containing one nitrogen atom and optionally 1-3 further heteroatoms chosen from oxygen, sulfur and nitrogen. Specific examples of such ring systems include, for example, indole, benzofuran, benzothiophene, benzimidazole, benzothiazole, benzisothiazole, benzoxazole, benzisoxazole, quinoline, quinoxaline, quinazoline, phthalazine and cinnoline. Other particular examples of AR3 include 5/5-, 5/6 and 6/6 bicyclic ring systems containing heteroatoms in both of the rings. Specific examples of such ring systems include, for example, purine and naphthyridine. Further particular examples of AR3 include bicyclic heteroaryl ring systems with at least one bridgehead nitrogen and optionally a further 1-3 heteroatoms chosen from oxygen, sulfur and nitrogen. Specific examples of such ring systems include, for example, 3H-pyrrolo[l,2-a]pyrrole, pyrrolo[2,l-b]thiazole, lH-imidazo[l,2-a]pyrroleJ lH-imidazo[l,2-a]imidazole5 lH,3H-pyrrolo[l,2-c]oxazole, lH-imidazo[l,5-a]pyrrole, pyrrolo[l,2-b]isoxazole, imidazo[5,l-b]thiazole, imidazo[2,l-b]thiazole, indolizine, imidazo[l,2-a]pyridine, imidazo[1,5-ajpyridine, pyrazolo[l,5-a]pyridine, pyrrolo[l,2-b]pyridazine, pyrrolo[l,2-c]pyrimidine, pyrrolo[l,2-a]pyrazme} pyirolo[l,2-a]pyrimidine, pyrido[2,l-c]-s-triazole, s-triazole[l,5-a]pyridine, inu^azo[l52-c]pyrimidine, imidazo[l,2-a]pyrazine, imidazo[l,2-a]pyrirnidine, imidazo[l,5-a]pyrazine, inn^azo[l,5-a]pyrimidine, imidazo[l,2-b]-pyridazine, s-triazolo[4}3-a]pyrimidine, imidazo[5,l-b]oxazole and imidazo[2,l-b]oxazole. Other specific examples of such ring systems include, for example, [lH]-pyrrolo[2,l-c]oxazine, [3H]-oxazolo[3,4-ajpyridine, [6H]-pyrrolo[2,l-c]oxazine andpyrido[2,l-c][l,4]oxazine. Other specific examples of 5/5- bicychc ring systems are imidazooxazole or imidazothiazole, in particular imidazo[5,l-b]thiazole, imidazo[2,l-b]thiazole, imidazo[5,l-b]oxazole or imidazo[2,l-b]oxazole. Particular examples of AR3a and AR3b include, for example, indoline, l,3,4,6,9,9a-hexahydropyrido[2,lc][l,4]oxazin-8-yl, 1,2,3,5,8,8a-hexahydroimidazo[l,5a]pyridin-7-yl, l,5,8,8a-tetrahydrooxazolo[3,4a]pyridin-7-yl, l,5,6,7,8,8a-hexahydiooxazolo[3,4a]pyridm-7-yl,(7aS)[3H,5H]-l,7a-dihydropyrrolo[l,2c]oxazol-6-yl, (7aS)[5H]-l,2,3,7a-tetrahydropyrrolo[l,2c]imidazol-6-yl (7aR)[3H,5H]-l,7a-dihyd^opyrrolo[l,2c]oxazol-6-yl,t3H,5Hl-pyrrolo[l,2-c]oxazol-6-yl, [5H]-2,3-dmydropyrrolo[l,2-c]iniidazol-6-yl,[3H,5H]-pyrrolo[l,2-c]una2ol-6-yl, [3H,5H]-l,7a-dmydropyrrolo[l,2-c]thiazol-6-yl, [5H]-pyrrolo[l,2-c]imidazol-6-yl, [lH]-3,4,8,8a- tetrahydropyrrolo[2,l-c]oxazm-7-yl, [3HJ-1,5,8a-tetrahydrooxazolo[3,4-a]pyrid-7yl,[3H]-5,8-dlhydroxazolo[3,4-a]pyrid-7-yl and5,8-dmydroiim\iazo[l,5-a]pyrid-7-yl. Particular values for AR.4 include, for example, pyrrolo[a]quinoline, 2,3-pyrroloisoquinoline, pyrrolo[a]isoquinoline, lH-pyrrolo[l ,2-a]benzhrridazole, 9H-inudazo[l,2-a]indole, 5H-iinidazo[2,l-a]isoindole, lH-imidazo[3,4-a]indole, imidazo[l,2-a)quinoline, imdazo[2,l-a]isoqumolme, imidazollj-ajqumoline and imidazo[5,1 -a]isoquinoline. Particular values of AR4a include partially hydrogenated version of those AR4 values listed immediately above. The nomenclature used is that found in, for example, "Heterocyclic Compounds (Systems with bridgehead nitrogen), WX.Mosby (Ihtercsience Publishers Inc., New York), 1961, Parts 1 and 2. Where optional substituents are listed such substitution is preferably not geminal disubstitution unless stated otherwise. If not stated elsewhere suitable optional substituents for a particular group are those as stated for similar groups herein. Suitable substituents on AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 are (on ah available carbon atom) up to three substituents independently selected from (l-4C)alkyl {optionally substituted by (preferably one) substituents selected independently from hydroxy, trifluoromethyl, (l-4C)aIkyl S(0)q- (q is 0,1 or 2) (this last substituent preferably on AR1 only), (l-4C)alkoxy, (l-4C)alkoxycarbonyl, cyano, nitro, (1-4C)alkanoylamino, -CONRvRw or -NRvRw}, trifluoromethyl, hydroxy, halo, nitro, cyano, thiol, (l-4C)alkoxy, (l-4C)alkanoyloxy, d^ethylarmnomethyleneaminocarbonyl, di(N-(l-4C)allsyl)aminomemylimino, carboxy, (l-4C)alkoxycarbonyl, (l-4C)alkanoyl, (1-4C)alfylS02amino, (2-4C)alkenyl {optionally substituted by carboxy or (1-4C)alkoxycarbonyl}, (2-4C)alkynyl, (l-4C)alkanoylamino3 oxo (=0), thioxo (=S), (1-4C)alkanoylamino {the (l-4C)alkanoyl group being optionally substituted by hydroxy}, (1-4C)alkyl S(0)q- (q is 0, 1 or 2) (the (l-4C)alkyl group being optionally substituted by one or more groups independently selected from cyano, hydroxy and (l-4C)alkoxy}, -CONRvRw or -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl]. Further suitable substituents on AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 (on an available carbon atom), and also on alkyl groups (unless indicated otherwise) are up to three substituents independently selected from trifluoromethoxy, benzoylamino, benzoyl, phenyl {optionally substituted by up to three substituents independently selected from halo, (l-4C)alkoxy or cyano}, ruran, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene, hydroxyimino(l-4C)alkyl, (l-4C)alkoxyimhio(l-4C)alkyl3 halo-(l-4C)alkyl, (l-4C)alkanesulfonamido, -S02NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkylj. Preferable optional substituents on Ar2b as l,3-dioxolan-4-yl, l,3-dioxan-4-yl, 1,3-dioxan-5-yl or l,4-dioxan-2-yl are mono- or disubstitution by substituents independently selected from (l-4C)alkyl (including geminal disubstitution), (l-4C)alkoxy, (l-4C)alkylthio, acetamido, (l-4C)alkanoyl, cyano, trifluoromethyl and phenyl]. Preferable optional substituents on CY1 & CY2 are mono- or disubstitution by substituents independently selected from (l-4C)alkyl (including geminal disubstitution), hydroxy, (l-4C)alkoxy, (l-4C)alkylthio, acetamido, (l-4C)alkanoyl, cyano, and trifluoromethyl. Suitable substituents on AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4 and AR4a are (on an available nitrogen atom, where such substitution does not result in quaternization) (1-4C)alkyl, (l-4C)alkanoyl {wherein the (l-4C)alkyl and (l-4C)alkanoyl groups are optionally substituted by (preferably one) substituents independently selected from cyano, hydroxy, nitro, trifluoromethyl, (l-4C)alkyl S(0)q- (q is 0,1 or 2), (l-4C)alkoxy, (1-4C)alkoxycarbonyL, (l-4C)alkanoylamino, -CONRvRw or -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl]}, (2-4C)alkenyl, (2-4C)alkynyl, (1-4C)alkoxycarbonyl or oxo (to form an N-oxide). Suitable pharmaceutically-acceptable salts include acid addition salts such as methanesulfonate, furnarate, hydrochloride, citrate, maleate, tartrate and (less preferably) hydrobromide. Also suitable are salts formed with phosphoric and sulfuric acid. In another aspect suitable salts are base salts such as an alkali metal salt for example sodium, an alkaline earth metal salt for example calcium or magnesium, an organic amine salt for example triethylamine, morpholine, N-methylpiperidine, N-ethylpiperidine, procaine, dibenzylamine, N,N-diben2ylemylamine, tris-(2-hydVoxyemyl)amineJ N-methyl d-glucamine and amino acids such as lysine. There may be more than one cation or anion depending on the number of charged functions and the valency of the cations or anions. A preferred pharmaceutically-acceptable salt is the sodium salt. However, to facilitate isolation of the salt during preparation, salts which are less soluble in the chosen solvent may be preferred whether pharmaceutically-acceptable or not. The compounds of the formula (I) may be administered in title form of a pro-drug which is broken down in the human or animal body to give a compound of the formula (I). A prodrug may be used to alter or improve the physical and/or pharmacokinetic profile of the parent compound and can be formed when the parent compound contains a suitable group or substituent which can be derivatised to form a prodrug. Examples of pro-drugs include in-vivo hydrolysable esters of a compound of the formula (J) or a pharmaceutically-acceptable salt thereof. Various forms of prodrugs are known in the art, for examples see: a) Design of Prodrugs, edited by H. Bundgaard, (Elsevier, 1985) and Methods in Enzymology, Vol. 42, p. 309-396, edited by K. Widder, et al (Academic Press, 1985); b) A Textbook of Drug Design and Development, edited by Krogsgaard-Larsen and H. Bundgaard, Chapter 5 "Design and Application of Prodrugs", by H. Bundgaard p. 113-191 (1991); c) H. Bundgaard, Advanced Drug Delivery Reviews, 8,1-38 (1992); d) H. Bundgaard, et al, Journal of Pharmaceutical Sciences, 22,285 (1988); and e) N.Kalceya,et al., Chem Pharm Bull, 32, 692(1984). An in-vivo hydrolysable ester of a compound of the formula (I) or a pharmaceutically-acceptable salt thereof containing carboxy or hydroxy group is, for example, a pharmaceutically-acceptable ester which is hydrolysed in the human or animal body to produce the parent acid or alcohol. Suitable pharmaceutically-acceptable esters for carboxy include (l-6C)alkoxymethyl esters for example methoxymethyl, (l-6C)allcanoyloxymethyl esters for example pivaloyloxymethyl, phthalidyl esters, (3-8C)cycloalkoxycarbonyloxy(l-6C)alkyl esters for example 1-cyclohexylcarbonyloxyethyl; l,3-dioxolan-2-onylmethyl esters for example 5-methyl-l,3-dioxolan-2-ylmethyl; and (l-6C)alkoxycarbonyloxyethyl esters for example 1-methoxycarbonyloxyethyl and may be formed at any carboxy group in the compounds of this invention. An in-vivo iiydrolysable ester of a compound of the formula (I) or a pharmaceutically-acceptable salt thereof containing a hydroxy group or groups includes inorganic esters such as phosphate esters (including phosphoramidic cyclic esters) and a-acyloxyalkyl ethers and related compounds which as a result of the in-vivo hydrolysis of the ester breakdown to give the parent hydroxy group/s. Examples of a-acyloxyalkyl ethers include acetoxymethoxy and 2,2-dimethylpropionyloxymethoxy. A selection of in-vivo hydrolysable ester forming groups for hydroxy include (l-10C)alkanoyl, benzoyl, phenylacetyl and substituted benzoyl and phenylacetyl, (l-lOC)alkoxycafhonyl (to give alkyl carbonate esters), di-(l-4C)alkylcarbamoyl andH-(di-(K4C)aUcylan3inoethyl)-H-(l-4C)alkylcarbamoyl (to give carbamates), di-(l-4C)alkylamin0acetyl and carboxyacetyl. Examples of ring substituents on phenylacetyl and benzoyl include chloroniethyl or aminomethyl, (l-4C)alkylaminomethyl and di-((l-4C)alkyl)aminomethyl, and morpholino or piperazino linked from a ring nitrogen atom via a methylene linking group to the 3- or 4-position of the benzoyl ring. Certain suitable in-vivo hydrolysable esters of a compound of the formula (T) are described within the definitions listed in this specification, for example esters described by the definition (Rc2d), and some groups within (Rc2c). Suitable in-vivo hydrolysable esters of a compound of the formula (T) are described as follows. For example, a 1,2-diol may be cyclised to form a cyclic ester of formula (PD1) or a pyrophosphate of formula (PD2) : (fcDl) (PP2) Particularly interesting ar^ such cyclised pro-drugs when the 1,2-diol is on a (1-4C)alkyl chain linked to a carbonyl group in a substituent of formula Re borne by a nitrogen atom in (TC4). Esters of compounds of formula (T) wherein the HO- function/s in (PD1) and (F&2) are protected? by (l~4C)allkyl) phenyl ar benzyl are useM intermediates for &e preparation of such pro-drugs. Further in-vivo hydrolysable esters include phosphoramidic esters, and also compounds of formula (T) in which any free hydroxy group independently forms aphosphoryl (npd is 1) or phosphiryl (npd is 0) ester of the formula (PD3): Useful intermediates for the preparation of such esters include compounds containing a group/s of formula (PD3) in which either or both of the -OH groups in (PD3) is independently protected by (l-4C)alkyl (such compounds also being interesting compounds in their own right), phenyl or phenyl-(l-4C)alkyl (such phenyl groups being optionally substituted by 1 or 2 groups independently selected from (l-4C)alkyl, nitro, halo and (1-4C)alkoxy). Thus, prodrugs containing groups such as (PD1), (PD2) and (PD3) may be prepared by reaction of a compound of formula (I) containing suitable hydroxy group/s with a suitably protected phosphorylating agent (for example, containing a chloro or dialtylamino leaving group), followed by oxidation (if necessary) and deprotection. When a compound of formula (I) contains a number of free hydroxy group, those groups not being converted into a prodrug functionality may be protected (for example, using a t-butyl-dimethylsilyl group), and later deprotected. Also, enzymatic methods may be used to selectively phosphorylate or dephosphorylate alcohol functionalities. Other interesting in-vivo hydrolysable esters include, for example, those in which Re is defined by, for example, R14C(0)0(l-6C)alkyI-CO- (wherein RI4is for example, benzyloxy-(l-4C)alkyl, or phenyl). Suitable substituents on a phenyl group in such esters include, for example, 4-(l-4C)piperazino-(l-4C)alkyl, piperazino-(l-4C)alkyl and morpholino-(l-4C)alkyl. Where pharrnaceutically-acceptable salts of an in-vivo hydrolysable ester may be formed this is achieved by conventional techniques. Thus, for example, compounds containing a group of formula (PD1), (PD2) and/or (PD3) may ionise (partially or fully) to form salts with an appropriate number of counter-ions. Thus, by way of example, if an in-vivo hydrolysable ester prodrug of a compound of formula (I) contains two (PD3) groups, there are four HO-P- functionalities present in the overall molecule, each of which may form an appropriate salt (i.e. the overall molecule may form, for example, a mono-, di-, tri- or tetra-sodium salt). The compounds of the present invention have a chiral centre at the C-5 position of the oxazolidinone ring. The pharmaceutically active enantiomer is of the formula (IA): The present invention includes the pure enantiomer depicted above or mixtures of the 5R and 5S enantiomers, for example a racemic mixture. If a mixture of enantiomers is used, a larger amount (depending upon the ratio of the enantiomers) will be required to achieve the same effect as the same weight of the pharmaceutically active enantiomer. For the avoidance of doubt the enantiomer depicted above is generally the 5(R) enantiomer, although certain compounds (such as HET as pyrid-2-one) are the 5(S) enantiomer. Examples of 5(S) compounds are illustrated in the accompanying non-limiting Examples. Furthermore, some compounds of the formula (I) may have other chiral centres. It is to be understood that the invention encompasses all such optical and diastereo-isomers, and racemic mixtures, that possess antibacterial activity. It is well known in the art how to prepare optically-active forms (for example by resolution of the racemic form by recrystallisation techniques, by chiral synthesis, by enzymatic resolution, by biotransformation or by chromatographic separation) and how to determine antibacterial activity as described hereinafter. The invention relates to all tautomeric forms of the compounds of the formula (I) that possess antibacterial activity. It is also to be understood that certain compounds of the formula (I) can exist in solvated as well as unsolvated forms such as, for example, hydrated forms. It is to be understood that the invention encompasses all such solvated forms which possess antibacterial activity. It is also to be understood that certain compounds of the formula (I) may exhibit polymorphism, and that the invention encompasses all such forms which possess antibacterial activity. As stated before, we have discovered a range of compounds that have good activity against a broad range of Gram-positive pathogens including organisms known to be resistant to most commonly used antibiotics. Physical and/or pharmacokinetic properties, for example increased stability to mammalian peptidase metabolism and a favourable toxicological profile are important features. Xhe following compounds possess favourable physical and/or pharmacokinetic properties and are preferred. Particularly preferred compounds of the invention comprise a compound of formula (I) or of formula (IP), or a pharmaceutically-acceptable salt or an in-vivo hydrolysable ester thereof, wherein the substituents Q, HEX, T and other substituents mentioned above have values disclosed hereinbefore, or any of the following values (which may be used where appropriate with any of the definitions and embodiments disclosed hereinbefore or hereinafter): Preferably Q is selected from Ql, Q2, Q4, Q6 and Q9; especially Ql, Q2 and Q9; more particularly Ql and Q2; and most preferably Q is Ql. Preferably X is selected from (XAf), (XDb) or (XC); especially groups (TAG), (XCb) and (XCc); more particularly (XC2), (XC3) and (XC4); and most preferably (XC5), (XC7) or (XC9), and most particularly (XC9) and (XC5). Especially preferred is each of these values of X when present in Ql and Q2, particularly in Ql. Preferable values for other substituents (which may be used where appropriate with any of the definitions and embodiments disclosed hereinbefore or hereinafter) are :-(aO) In. one embodiment HEX is a 6-membered heteroaryl ring as defined herein, and in another embodiment HEX is a 5-membered heteroaryl ring as defined herein. Preferably HEX is a 5-membered heteroaryl as defined herein. In this specification it will be appreciated that when HEX is a 5-membered heteroaryl ring, the ring must be aromatic and that when HEX is a 6-membered heteroaryl ring, the ring system (which contains the optimum number of double bonds) can necessarily only be pseudoaromatic. It will also be appreciated that when HEX as an N-linked 5-membered heteroaryl ring is optionally substituted on an available carbon atom by oxo or tbioxo then, when HEX contains 1 to 3 further nitrogen heteroatoms, one of the further nitrogen heteroatoms is present as NH or as N-(l-4C)alkyl. Similarly, when HEX as an N-linked 5-membered heteroaryl ring is optionally substituted on an available nitrogen atom by (1-4C)alkyl then the ring is substituted on an available carbon atom by oxo or thioxo. (a) When HEX is a 6-membered heteroaryl as defined herein, preferably HEX is pyridine or pyridazine; preferably with a 2-oxo substituent. (b) When HEX is a 5-membered heteroaryl as defined herein, preferably HEX contains only nitrogen heteroatoms or is thiadiazole or thiazole. > (c) Yet more preferably HEX is triazole, tetrazole or imidazole, especially triazole or tetrazole, and most especially triazole. (d) Further preferred as HEX is 1,2,3-triazole and 1,2,4-triazole, especially 1,2,3-triazole, and most especially 1,2,3-triazol-l-yl. (e) Further preferred as HEX is 1,2,3,4-tetrazole, especially l,2,3,4-tetrazol-2-yl. (f) Most preferred is HET as 1,2,3-triazol-l-yl. (g) Preferably HEX (when a 5-membered ring) is unsubstituted. (h) Preferably R6p is hydrogen; (i) Preferably R4p and R5p are independently selected from hydrogen, (l-4C)alkyl, carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (l-4C)alkoxymethyl or carbamoyl; (j) More preferably R4p and R5p are hydrogen; (k) Preferably R2 and R3 are hydrogen or fluoro; (1) In one aspect of the invention more preferably one of R2 and R3 is hydrogen and the other fluoro. In another aspect of the invention both R2 and R3 are fluoro; (m) Preferably >A-B- is of the formula >C=CH- (i.e. Ra is preferably hydrogen) or>N-CH2-; (n) Preferably D is 0 or NR7p; (o) Preferably R7p is ARp, R10pCO-, RI0pSO2-, R10pCS-; (p) More preferably R7p is ARp (most preferably benzyl, pyrimidyl, pyridinyl, pyridazinyl or pyrazinyl) or R10pCO-; (q) Particularly R7p is R10pCO-; (ql) Especially preferred is R10pCO- (or R13CO-) wherein R10p (or R13) is (l-lO)alkyl optionally substituted by hydroxy or (l-4C)alkylS(0)q- (wherein q is 0,1 or 2), wherein the (l-4C)alkyl group is optionally substituted as defined herein for this particular substituent; (r) Preferably ARp is 5- or 6-membered heteroaryl; more preferably ARp is 6-membered heteroaryl, such as pyridinyl; (s) Preferred substituents for phenyl and carbon atoms in heteroaryl (mono- and bicyclic) ring systems in ARp, Rllp and R1 include halo, (l-4C)alkyl, hydroxy, nitro, amino, cyano, (l-4C)alkylS(0)p- and (l-4C)alkoxy; (t) Preferably the optionally substituted ring systems in ARp, R1 lp and R1 are unsubstituted; (u) In another embodiment in the definition of R10p in (PC) of embodiment (IP), 1,3- dioxolan-4-yl and l,4-dioxan-2-yl are excluded. (v) In one aspect of the invention, preferably R10p is (l-4C)alkoxycarbonyl, hydroxy(l-4C)alkyl, (l-4C)alkyl (optionally substituted by one or two hydroxy groups, or by an (l-4C)alkanoyl group), (l-4C)alkylamino, dimemylamino(l-4C)allcyl, (L-4C)alkoxymethyl, (l-4C)alkanoylmethyl, (l-4C)alkanoyloxy(l-4C)alkyl, (l-5C)alkoxy or 2-cyanoethyl; (w) In one aspect of the invention, more preferably R10p is 1,2-dihydroxyethyl, l,3-dihydroxyprop-2-yl, 1,2,3-trihydroxyprop-l-yl, methoxycarbonyl, hydroxymethyl, methyl, memylamino, dimemylaminomethyl, methoxymethyl, acetoxymethyl, methoxy, methylthio, naphthyl, tert-butoxy or 2rcyanoethyl; (x) In one aspect of the invention, particularly R10p is 1,2-dihydroxyethyl, l,3-dihydroxyprop-2-yl or 1,2,3-trihydroxyprop-l-yl; (y) In another aspect of the invention preferably R10p is hydrogen, (1-1 OQalkyl [optionally substituted by one or more hydroxy] or RllpC(0)0(l-6C)alkyl. (z) In another aspect of the invention, more preferably R10p is hydrogen, hydroxymethyl, 1,2-dihydroxyethyl or acteoxyacetyl; and/or Rc2c is (l-10C)alkyl optionally substituted by (1- 4C)alkyl S(0)q-(q is 0-2), optionally substituted as in claim 1. (aa) Preferably Rup is (1-1 OQalkyl; . (ab) Preferred optional substituents for (1 -10C)aliyl in Rllp are hydroxy, cyano, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino9 (l-4C)alkylS(0)p (wherein p is 1 or 2), carboxy, (l-4C)alkoxycarbonyl, (l-4C)alkoxy, piperazino or morpholino; (m) Preferred optional substituents for (1 -6C)alkyl in R12p are hydroxy, (1 -4C)alkoxy, cyano, amino, (l-4C)all{ylamino, di((l-2C)alkyl)amino, (l-4C)alkylS(0)p- (wherein p is 1 or 2); (n) Preferably 5- or 6-membered heteroaryl in Rllp is pyridinyl or imidazoH-yl; (o) Preferably R12p is (l-6C)alkyl; most preferably R,2p is lert-butyl or methyl; (at) Preferably R13p is cyano or fluoro; (ag) Preferably R,4p is hydrogen; (ah) Preferably CYp is naphthoxy, especially naphth-1 -oxy or naphth-2-oxy. Where preferable values are given for substituents in a compound of formula (IP), the corresponding substituents in a compound of formula (I) have the same preferable values (thus, for example, Re and R13 in formula (I) correspond with R7p and R,0p in formula (DP), and similarly for groups D and G). The preferred values of R71, for example, defined with reference to (IP) are also preferred values of Re and may be used as preferred values of Re in any compound of formula (I). For compounds of formula (T) preferred values for Re are those in group (Rc2) when present in any of the definitions herein containing Re - for example when present in compounds in which there is a (TC5) or (TC9) ring system. The preferred values for R10p listed above for compounds of formula (D?) are also preferred values for R13 in compounds of formula (I). In the definition of (Rc2c) the AR2a, AR2b, AR3a and AR3b versions of AR2 and AR3 containing groups are preferably excluded. Particularly, HET (when substituted) is selected from the following 7 rings (HET-P1 to HET-P7) :- The above HET definitions are especially preferred in embodiment (IP). Especially preferred compounds of the present invention are of the formula (EB): wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fiuoro; and Rpl and Rp2 are independently hydrogen, hydroxy, bromo, (l-4C)alkyl, carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (1-4C)alkoxymethyl or carbamoyl; or pharmaceutically-acceptable salts thereof. Further especially preferred compounds of the invention are of the formula (IB) wherein HET is wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fiuoro; and Rpl and Rp2 are independently hydrogen, AR-oxymethyl or AR-thiomethyl (wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrirnidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene); or pharmaceutically-acceptable salts thereof. Of the above especially preferred compounds of the invention of the formula (IB), particularly preferred compounds are those wherein Rpl and Rp2 are hydrogen are particularly preferred. Further especially preferred compounds of the present invention are of the formula (T3-1): (IB-1) wherein HET is triazole or tetrazole, and most especially triazole (particularly 1,2,3-triazole, and especially 1,2,3-triazoI-l-yI); R2 and R3 are independently hydrogen or fluoro and p is 1 or 2. Further, especially preferred compounds of the invention are of the formula (IC): Rp1 R2 (IC) wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are independently hydrogen, AR-oxymethyl or AR-thiomethyl (wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene), (l-4C)allcyl, carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (1-4C)alkoxymethyl or carbamoyl and Rep is cyano, pyrimidin-2-yl, 2-cyanoethenyl, 2-cyano-2- ((l-4C)allcyl)ethenyl or Rep is of the formula R10pCO-, R10pSO2- or R,0pCS- (wherein R10p is hydrogen, (l-5C)alkyl [optionally substituted by one or more groups each independently selected from hydroxy and amino, or optionally monosubstituted by (l-4C)alkoxy, (1-4C)alkylS(0)q-, (l-4C)alkylarnino, (l-4C)alkanoyl, naphthoxy, (2-6C)aUcanoylamino or (1-4C)alkylS(0)pNH- wherein p is 1 or 2 and q is 0,1 or 2], imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, pyridoimidazole, pyrimidoimidazole, quinoxaline, quinazoline, phthalazine, cinnoline or naphthyridine, or R10p is of the formula RllpC(0)0(l-6C)alkyl wherein Rllp is (l-6C)allcyl), or Rep is of the formula RfC(=0)C(=0)- wherein Rf is (l-6C)alkoxy; orpharmaceutically-acceptable salts thereof. Of the above especially preferred compounds of the invention of the formula (IC), ' those wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are independently hydrogen, AR-oxymethyl or AR-thiomethyl (wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrirnidine, pyiidazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene), (l-4C)alkyl, carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (1-4C)aIkoxymethyl or carbamoyl and Rep is cyano, pyrirnidin-2-yl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl or Rep is of the formula R10pCO-, R,0pSO2- or R10pCS- (wherein R,10p is hydrogen, (l-5C)alkyl [optionally substituted by one or more groups each independently selected from hydroxy and amino, or optionally monosubstituted by (l-4C)alkoxy, (1-4C)alkylS(0)q, (l-4C)alkylarnino, (l-4C)alkanoyl, (2-6C)alkanoylamino or (1-4C)alkylS(0)pNH- wherein p is 1 or 2 and q is 0,1 or 2], pyridine, or R10p is of the formula RllpC(0)0(l-6C)allcyl wherein RUp is (l-6C)alkyl), or Rep is of the formula RfC(=0)C(=0)-whereinRf is (l-6C)alkoxy; or pharmaceutically-acceptable salts thereof are further preferred. Of the above especially preferred compounds of the invention of the formula (IC), particularly preferred compounds are those wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are hydrogen, and Rep is pyridin-2-yl (optionally substituted with cyano) or Rcp is of the formula R10pCO- (wherein R10p is hydrogen, l,3-dioxolan-4-yl (optionally disubstituted with (1-4C)alkyl) or (l-5C)allkyl [optionally substituted by one or more hydroxy groups] or R10p is of the formula RllpC(0)0(l-6C)alkyl wherein R11p is (l-6C)alkyl)); or pharmaceutically-acceptable salts thereof. Of the above especially preferred compounds of the invention of the formula (IC), particularly preferred compounds are those wherein Rep is of the formula R10pCO- (wherein R10p is hydrogen, l,3-dioxolan-4-yl (optionally disubstituted with (l-4C)alkyl) or (l-5C)alkyl [substituted by two hydroxy groups, e.g. 2,3-dihydroxypropanoyl or by one hydroxy group, e.g. hydroxyacetyl]; or pharmaceutically-acceptable salts thereof. In another aspect of the invention particularly preferred compounds of the invention are of the formula (IC) wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are hydrogen and Rep is R10pCO-(wherein R10p is hydrogen, (l-5C)alkyl [optionally substituted by one or two hydroxy groups], or Rl0p is of the formula RllpC(0)0(l-6C)alkyl (wherein RUp is (l-6C)alkyl)); and pharmaceutically-acceptable salts thereof. In another aspect of the invention all of the compounds of formula (IB) or (IC) described above are further preferred when HET is triazole. In yet another aspect the invention relates to all of the compounds of formula (IB) or (IC) described above wherein HET is 1,2,3-triazoM-yl. In another aspect of the invention there are provided preferred compounds of the formula (IP) wherein HET is triazole or tetrazole, and most especially triazole; >A-B- is >N-CH2- and D is NR7p (or D is O) wherein Rep is a 6-membered heteroaiyl ring containing 1,2 or 3 ring nitrogen atoms as the only ring heteroatoms, linked via a ring carbon atom and optionally substituted on a ring carbon atom by one, two or three substituents independently selected from (l-4C)alkyl, halo, trifluoromethyl, (l-4C)alkyl S(0)q- (wherein q is 0,1 or 2), (l-4C)aIkylS(0)2amino, (l-4C)aUcanoylarnino, carboxy, hydroxy, amino, (l-4C)alkylairiino, di-(l-4C)altylamino, (MQalkoxycarbonyl, carbamoyl, K-(l-4C)alkylcarbamoyl, di-(N-(l-4C)aIkyl)carbamoyl, (l-4C)alkoxy, cyano or nitro; or pharmaceutically-acceptable salts thereof. In yet another aspect the invention relates to all of the compounds of formula (IP) described immediately above wherein >A-B- is >N-CH2- and D is NR7p and wherein HET is triazole or tetrazole, and most especially triazole. In all of the above aspects and preferred compounds of formula (IB) or (IC), in-vivo hydrolysable esters are preferred where appropriate, especially phosphoryl esters (as defined by formula (PD3) with npd as 1). In all of the above definitions the preferred compounds are as shown in formula (IA), i.e. the pharmaceutically active (5(R)) enantiomer. Particular compounds of the present invention include the compounds of Examples 34b, 44a, 52, 54,56, 58, 64 and 74 (wherein "a" refers to the first named compound, and "b" the second named compound in the Example title); or pharmaceutically-acceptable salts thereof. Particularly preferred salts are the sodium salts. In-vivo hydrolysable esters, or pharmaceutically-acceptable salts thereof, of Examples with hydroxy groups are also preferred, especially phosphoryl esters. In a further aspect the present invention provides a process for preparing a compound of formula (I) or a pharmaceutically-acceptable salt or an in-vivo hydrolysable ester thereof. It will be appreciated that during certain of the following processes certain substituents may require protection to prevent their undesired reaction. The skilled chemist will appreciate when such protection is required, and how such protecting groups may be put in place, and later removed. For examples of protecting groups see one of the many general texts on the subject, for example, 'Protective Groups in Organic Synthesis' by Theodora Green (publisher: John Wiley » & Sons). Protecting groups may be removed by any convenient method as described in the literature or known to the skilled chemist as appropriate for the removal of the protecting group in question, such methods being chosen so as to effect removal of the protecting group with minimum disturbance of groups elsewhere in the molecule. Thus, if reactants include, for example, groups such as amino, carboxy or hydroxy it may be desirable to protect the group in some of the reactions mentioned herein. A suitable protecting group for an amino or alkylamino group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an alkoxycarbonyl group, for example a methoxycarbonyl, ethoxycarbonyl or /-butoxycarbonyl group, an aiylmethoxycarbonyl group, for example benzyloxycarbonyl, or an aroyl group, for example benzoyl. The deprotection conditions for the above protecting groups necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or alkoxycarbonyl group or an aroyl group may be removed for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide. Alternatively an acyl group such as a f-butoxycarbonyl group may be removed, for example, by treatment with a suitable acid as hydrochloric, sulfuric or phosphoric acid or trifluoroacetic acid and an arylmethoxycarbonyl group such as a benzyloxycarbonyl group may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon, or by treatment with a Lewis acid for example boron tris(rrifluoroacetate). A suitable alternative protecting group for a primary amino group is, for example, a phthaloyl group which may be removed by treatment with an alkylamine, for example dimemylammopropylamine, or with hydrazine. A suitable protecting group for a hydroxy group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an aroyl group, for example benzoyl, or an arylmethyl group, for example benzyl. The deprotection conditions for the above protecting groups will necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or an aroyl group may be removed, for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example Hthium or sodium hydroxide. Alternatively an arylmethyl group such as a benzyl group may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon. A suitable protecting group for a carboxy group is, for example, an esterifying group, for example a methyl or an ethyl group which may be removed, for example, by hydrolysis with a base such as sodium hydroxide, or for example a f-butyl group which may be removed, for example, by treatment with an acid, for example an organic acid such as trifiuoroacetic acid, or for example a benzyl group which may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon. Resins may also be used as a protecting group. The protecting groups may be removed at any convenient stage in the synthesis using conventional techniques well known in the chemical art. A compound of the formula (I), or a pharmaceutically-acceptable salt or an in vivo hydrolysable ester thereof, may be prepared by any process known to be applicable to the preparation of chemically-related compounds. Such processes, when used to prepare a compound of the formula (I), or a pharmaceutically-acceptable salt or an in vivo hydrolysable ester thereof, are provided as a further feature of the invention and are illustrated by the following representative examples. Necessary starting materials may be obtained by standard procedures of organic chemistry (see, for example, Advanced Organic Chemistry (Wiley-[nterscience), Jerry March). The preparation of such starting materials is described within the accompanying non-limiting Examples (in which, for example, 3,5-difluorophenyl, 3-Quorophenyl and (des-fluoro)phenyl containing intermediates may all be prepared by malagous procedures; or by alternative procedures - for example, the preparation of (T jroup)-(fluoro)phenyl intermediates by reaction of a (fluoro)phenylstannane with, for jxample, a pyran or (tetrahydro)pyridine compound, may also be prepared by anion chemistry see, for example, WO97/30995). Alternatively, necessary starting materials are obtainable by analogous procedures to those illustrated which are within the ordinary skill of an organic chemist. Information on the preparation of necessary starting materials or related compounds (which may be adapted to form necessary starting materials) may also be found in the following Patent and Application Publications, the contents of the relevant process sections of which are hereby incorporated herein by reference : WO99/02525; W098/54161; WO97/37980; WO97/30981 (& US5,736,545); WO97/21708 (& US5,719,154); WO97/10223; WO97/09328; W096V35691; W096/23788; WO96/15130; WO96/13502; WO95/25106 (& US5,668,286); W095/14684 (& US5,652,238); WO95/07271 (& USS,688,792); W094/13649; WO94/01110; W093/23384 (& US5,547,950 & US 5,700,799); WO93/09103 (&US5,565,571, US5,654,428, US5,654,435, US5,756,732 & US5,801,246); US5,231,188; US5,247,090; US5,523,403; W097/27188; WO97/30995; W097/31917; WO98/01447; WO98/01446; WO99/10342; WO99/10343; W099/11642; W099/64416; W099/64417 and GB99/03299; European Patent Application Nos. 0,359,418 and 0,609,905; 0,693,491 Al (& US5,698,574); 0,694,543 Al (& AU 24985/95); 0,694,544 Al (& CA 2,154,024); 0,697,412 Al (& US5,529,998); 0,738,726 Al (& AU 50735/96); 0,785,201 Al (& AU 10123/97); German Patent Application Nos. DE 195 14 313 Al (& US5,529,998); DE 196 01 264 Al (& AU 10098/97); DE 196 01 265 Al (& AU 10097/97); DE 196 04 223 Al (& AU 12516/97); DE 196 49 095 Al (& AU 12517/97). The following Patent and Application Publications may also provide useful information and the contents of the relevant process sections are hereby incorporated herein by reference : FR 2458547; FR2500450(& GB 2094299, GB 2141716 & US 4,476,136); DE 2923295 (& GB 2028306, GB 2054575, US4,287,351, US4,348,393, US4,413,001, US4,435,415 & US4,526,786), DE 3017499 (& GB 2053196, US4,346,102 & US4,372,967); US4,705,799; European Patent Application Nos. 0,312,000; 0,127,902; 0,184,170; 0,352,781; 0,316,594; The skilled organic chemist will be able to use and adapt the information contained and referenced within the above references, and accompanying Examples therein and also the Examples herein, to obtain necessary starting materials, and products. Thus, the present invention also provides that the compounds of the formulae (!) and pharmaceutically-acceptable salts and in vivo hydrolysable esters thereof, can be prepared by a process (a) to (d) as follows (wherein the variables are as defined above unless otherwise stated): (wherein the variables are as defined above unless otherwise stated) : (a) by modifying a substituent in or introducing a substituent into another compound of formula (E); (b) by reaction of a compound of formula (IT): wherein Y is a displaceable group (which may be preformed, such as chloro or mesylate, or generated in-situ, for example under Mitsunobu conditions) with a compound of the formula (TO) : HET OH) wherein HET is HET-H free-base form or HET- anion formed from the free base form; or . (c) by reaction of a compound of the formula (TV) : Q-Z dV) wherein Z is an isocyanate, amine or urethane group with an epoxide of the formula (V) : (d) For the 1,2,3-triazoles there is the additional possibility by cycloaddition via the azide (wherein Y in (II) is azide); and thereafter if necessary: (i) removing any protecting groups; (ii) forming a pharmaceuticaUy-acceptable salt; (iii) forming an in-vivo hydrolysable ester. The main synthetic routes are illustrated in the Scheme below (with Q as phenyl, and X, R and A defined with reference to analogous substituents defined elsewhere herein). The compounds of the invention maybe prepared by analogous chemistry adapted from this Scheme. The Scheme also shows the preparation of 1,2,3-triazoles via the azide (prepared from the relevant hydroxy compound). Deprotection, salt formation or in-vivo hydrolysable ester formation may each be provided as a specific final process step. The N-linked hetereocycle can of course be prepared early in the overall synthesis, and then other functional groups changed. Where Y is a displaceable group, suitable values for Y are for example, a halogeno or sulfonyloxy group, for example a chloro, bromo, methanesulfonyloxy or toluene-4-. sulfonyloxy group. General guidance on reaction conditions and reagents may be obtained in Advanced Organic Chemistry, 4th Edition, Jerry March (publisher : J.Wiley & Sons), 1992. Necessary starting materials may be obtained by standard procedures of organic chemistry, such as described in this process section, in the Examples section or by analogous procedures within the ordinary skill of an organic chemist. Certain references are also provided which describe the preparation of certain suitable starting materials, for example International Patent Application Publication No. WO 97/37980, the contents of which are incorporated here by reference. Processes analogous to those described in the references may also be used by the ordinary organic chemist to obtain necessary starting materials. (a) Methods for converting substituents into other substituents are known in the art. For example an alkylthio group may be oxidised to an alkylsulfinyl or alkysulfonyl group, a cyano group reduced to an amino group, a nitro group reduced to an amino group, a hydroxy group alkylated to a methoxy group, a hydroxy group thiomethylated to an arylthiomethyl or a heteroarylthiomethyl group (see, for example, TetXett., 585,1972), a carbonyl group converted to a thiocarbonyl group (eg. using Lawsson's reagent) or a bromo group converted to an alkylthio group. It is also possible to convert one Re group into another Re group as a final step in the preparation of a compound of the formula (I), for example, acylation of a group of formula (TC5) wherein Re is hydrogen. (b)( i) Reaction (b)(i) (in which Y is initially hydroxy) is performed under Mitsunobu conditions, for example, in the presence of tri-n-butylphosphine and diethyl azodicarboxylate (DEAD) in an organic solvent such as THF, and in the temperature range 0°C - 60°C, but preferably at ambient temperature. Details of Mitsunobu reactions are contained in Tet. Letts., 21,699, (1990); The Mitsunobu Reaction, D.L.Hughes, Organic Reactions, 1992, Vol.42, 335-656 and Progress in the Mitsunobu Reaction, D.L.Hughes, Organic Preparations and Procedures International, 1996, Vol.28,127-164. Compounds of the formula (H) wherein Y is hydroxy may be obtained as described in the references cited herein (particularly in the section proceeding the discussion of protecting groups), for example, by reacting a compound ef the formula (VI) with a compound of formula (VII): wherein R21 is (l-6C)alkyl or benzyl and R22 is (l-4C)aIkyl or -S(0)„(l-4C)alkyl where n is 0, 1 or 2. Preferably R22 is (l-4C)alkyI. In particular, compounds of the formula (IT), (VI) and (VII) may be prepared by the skilled man, for example as described in International Patent Application Publication Nos. WO95/07271, W097/27188, WO 97/30995, WO 98/01446 and WO 98/01446, the contents of which are hereby incorporated by reference, and by analogous processes. If not commercially available, compounds of the formula (IE) may be prepared by procedures which are selected from standard chemical techniques, techniques which are analogous to the synthesis of known, structurally similar compounds, or techniques which are analogous to the procedures described in the Examples. For example, standard chemical techniques are as described in Houben Weyl, Methoden der Organische Chemie, E8a, Pt.I (1993), 45-225, B.J.Wakefield. (b)( ii) Reactions (b)(ii) are performed conveniently in the presence of a suitable base such as, for example, an alkali or alkaline earth metal carbonate, alkoxide or hydroxide, for example sodium carbonate or potassium carbonate, or, for example, an organic amine base such as, for example, pyridine, 2,6-lutidine, collidine, 4-dimethylarninopyridine, Memylamine, morpholine or diazabicyclo-[5.4.0]undec-7-ene, the reaction is also preferably carried out in a suitable inert solvent or diluent, for example methylene chloride, acetonitrile, tetrahydrofuran, 1,2-dimethoxyethane, N N-dmiethylfomamLde, N,N-dtrnethylacetamide, N-methylpyrrolidin-2-one or dhnethylsulfoxide at and at a temperature in the range 25-60°C. When Y is chloro, the compound of the formula (II) may be formed by reacting a compound of the formula (11) wherein Y is hydroxy (hydroxy compound) with a chlorinating agent. For example, by reacting the hydroxy compound with thionyl chloride, in a temperature range of ambient temperature to reflux, optionally in a chlorinated solvent such as dichloromethane or by reacting the hydroxy compound with carbon tetrachloride/triphenyl phosphine in dichloromethane, in a temperature range of 0°C to ambient temperature. A compound of the formula (II) wherein Y is chloro or iodo may also be prepared from a compound of the formula (II) wherein Y is mesylate or tosylate, by reacting the latter compound with lithium chloride or hthium iodide and crown ether, in a suitable organic solvent such as THF, in a temperature range of ambient temperature to reflux When Y is (l-4C)alkanesulfonyloxy or tosylate the compound (H) may be prepared by reacting the hydroxy compound with (l-4C)alkanesulfonyl chloride or tosyl chloride in the presence of a mild base such as triemylamine or pyridine. When Y is a phosphoryl ester (such as Ph02-P(0)-0-) or Pb2-P(0)-0- the compound (II) may be prepared from the hydroxy compound under standard conditions. (c) Reaction (c) is performed under conditions analogous to those described in the following references which disclose how suitable and analogous starting materials may be obtained. Reaction (c) is especially suitable for compounds in which HET is an electron deficient heteroaryl (such as, for example, thiadiazole or triazine). Compounds of the formula Q-Z wherein Z is an isocyanate may be prepared by the skilled chemist, for example by analogous processes to those described in Walter A. Gregory et al in J. Med. Chem. 1990, 33,2569-2578 and Chung-Ho Park et al in J. Med. Chem. 1992, 35,1156-1165. Compounds of the formula Q-Z wherein Z is a urethane may be prepared by the skilled chemist, for example by analogous processes to those described in International Patent Application Publication Nos. WO 97/30995 and WO 97/37980., A similar reaction to reaction (c) may be performed in which Q-Z wherein Z is a amine group is reacted with the epoxide (optionally in the presence of an organic base), and the product is reacted with, for example, phosgene to form the oxazolidinone ring. Such reactions and the preparation of starting materials in within the skill of the ordinary chemist with reference to the above-cited documents disclosing analogous reactions and preparations. Epoxides of the formula (V) may be prepared from the corresponding compound of formula (VIH): Certain such epoxide and alkene intennediates are novel and are provided as a further feature of the invention. Asymmetric epoxidation may be used to give the desired optical isomer. (d) The cycloaddition reaction to form 1,2,3 triazoles from the corresponding azide is performed under conventional conditions. Compounds of the formula (II) wherein Y is azide may be obtained as described in the references cited herein (particularly in the section proceeding the discussion of protecting groups), for example from the corresponding compounds in which Y is hydroxy or mesylate. The removal of any protecting groups, the formation of apharmaceutically-acceptable salt and/or the formation of an in vivo hydrolysable ester are within the skill of an ordinary organic chemist using standard techniques. Furthermore, details on the these steps, for example the preparation of in-vivo hydrolysable ester prodrugs has been provided in the section above on such esters, and in certain of the following non-limiting Examples. When an optically active form of a compound of the formula (T) is required, it may be obtained by carrying out one of the above procedures using an optically active starting material (formed, for example, by asymmetric induction of a suitable reaction step), or by resolution of a racemic form of the compound or intermediate using a standard procedure, or by chromatographic separation of diastereoisomers (when produced). Enzymatic techniques may also be useful for the preparation of optically active compounds and/or intermediates. Similarly, when a pure regioisomer of a compound of the formula (I) is required, it may be obtained by carrying out one of the above procedures using a pure regioisomer as a starting material, or by resolution of a mixture of the regioisomers or intermediates using a. standard procedure. According to a further feature of the invention there is provided a compound of the formula (I), or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof for use in a method of treatment of the human or animal body by therapy. According to a further feature of the present invention there is provided a method for producing an antibacterial effect in a warm blooded animal, such as man, in need of such treatment, which comprises administering to said animal an effective amount of a compound of the present invention, or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof. The invention also provides a compound of the formula (I), or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof, for use as a medicament; and the use of a compound of the formula (I) of the present invention, or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof, in the manufacture of a medicament for use in the production of an antibacterial effect in a warm blooded animal, such as man. In order to use a compound of the formula (I), an in-vivo hydrolysable ester or a pharmaceutically-acceptable salt thereof, including a pharmaceutically-acceptable salt of an in-vivo hydrolysable ester, (hereinafter in this section relating to pharmaceutical composition "a compound of this invention") for the therapeutic (including prophylactic) treatment of mammals including humans, in particular in treating infection, it is normally formulated in accordance with standard pharmaceutical practice as a pharmaceutical composition. Therefore in another aspect the present invention provides a pharmaceutical composition which comprises a compound of the formula (I), an in-vivo hydrolysable ester or a pharmaceutically-acceptable salt thereof, including a pharmaceutically-acceptable salt of an in-vivo hydrolysable ester, and a pharmaceutically-acceptable diluent or carrier. The pharmaceutical compositions of this invention may be administered in standard manner for the disease condition that it is desired to treat, for example by oral, rectal or parenteral adrninistration. For these purposes the compounds of this invention may be formulated by means known in the art into the form of, for example, tablets, capsules, aqueous or oily solutions or suspensions, (lipid) emulsions, dispersible powders, suppositories, ointments, creams, aerosols (or sprays), drops and sterile injectable aqueous or oily solutions or suspensions. In addition to the compounds of the present invention the pharmaceutical compositio of this invention may also contain or be co-administered (simultaneously, sequentially or separately) with one or more known drugs selected from other clinically useful antibacterial agents (for example, B-lactams or aminoglycosides) and/or other anti-infective agents (for i example, an antifungal triazole or amphotericin). These may include carbapenems, for example meropenem or imipenem, to broaden the therapeutic effectiveness. Compounds of this invention may also contain or be co-administered with bactericidal/permeability-increasing protein (BPI) products or efflux pump inhibitors to improve activity against gram negative bacteria and bacteria resistant to antimicrobial agents. A suitable pharmaceutical composition of this invention is one suitable for oral administration in unit dosage form, for example a tablet or capsule which contains between lmg and lg of a compound of this invention, preferably between lOOmg and lg of a compound. Especially preferred is a tablet or capsule which contains between 50mg and 800mg of a compound of this invention, particularly in the range lOOmg to 500mg. In another aspect a pharmaceutical composition of the invention is one suitable for intravenous, subcutaneous or intramuscular injection, for example an injection which contam between 0.1% w/v and 50% w/v (between lmg/ml and 500mg/ml) of a compound of this invention. Each patient may receive, for example, a daily intravenous, subcutaneous or intramuscular dose of 0.5 mgkg-1 to 20 mgkg-1 of a compound of this invention, the composition being administered 1 to 4 times per day. In another embodiment a daily dose of i mgkg-1 to 20 mgkg-1 of a compound of this invention is administered. The intravenous, subcutaneous and intramuscular dose may be given by means of a bolus injection. Alternatively the intravenous dose may be given by continuous infusion over a period of time, Alternatively each patient may receive a daily oral dose which may be approximately equivalent to the daily parenteral dose, the composition being administered 1 to 4 times per day. A pharmaceutical composition to be dosed intravenously may contain advantageously (for example to enhance stability) a suitable bactericide, antioxidant or reducing agent, or a suitable sequestering agent. In the above other, pharmaceutical composition, process, method, use and medicament manufacture features, the alternative and preferred embodiments of the compounds of the invention described herein also apply. Antibacterial Activity: The pharmaceutically-acceptable compounds of the present invention are useful antibacterial agents having a good spectrum of activity in vitro against standard Gram-positive organisms, which are used to screen for activity against pathogenic bacteria. Notably, the pharmaceutically-acceptable compounds of the present invention show activity against enterococci, pneumococci and methicillin resistant strains of S.aureus and coagulase negative staphylococci, together with haemophilus and moraxella strains. The antibacterial spectrum and potency of a particular compound may be determined in a standard test system. The (antibacterial) properties of the compounds of the invention may also be demonstrated and assessed in-vivo in conventional tests, for example by oral and/or intravenous dosing of a compound to a warm-blooded mammal using standard techniques. The following results were obtained on a standard in-vitro test system. The activity is described in terms of the minimum inhibitory concentration (MIC) determined by the agar-dilution technique with an inoculum size of 104 CFU/spot. Typically, compounds are active in the range 0.01 to 256 \|xg/ml. Staphylococci were tested on agar, using an inoculum of 104 CFU/spot and an incubation temperature of 37°C for 24 hours - standard test conditions for the expression of methicillin resistance. Streptococci and enterococci were tested on agar supplemented with 5% defibrinatec horse blood, an inoculum of 10^ CFU/spot and an incubation temperature of 37°C in an atmosphere of 5% carbon dioxide for 48 hours - blood is required for the growth of some of the test organisms. Fastidious Gram negative organisms were tested in Mueller-Hinton brotli, supplemented with hemin and NAD, grown aerobically for 24 hours at 37°C, and with an innoculum of 5x104 CFU/well. For example, the following results were obtained for the compound of Example 44a: MICQig/mj) 0.125 0.25 0.25 0.06 0.13 Organism Staphylococcus aureus: , Oxford Novb. Res MRQR Coagulase Negative Staphylococci MS MR 0.25 0.25 0.25 2 2 Streptococcus pyogenes C203 Enterococcus faecalis Bacillus subtilis Haemophilus influenzae ARC446 Moraxella catarrhalis ARC445 Novb. Res - Novobiocin resistant MRQR - methicillin and quinolone resistant MR = methicillin resistant MS = methicillin sensitive Certain intermediates and/or Reference Examples described hereinafter within the scope of the invention may also possess useful activity, and are provided as a further feature of the invention. The invention is now illustrated but not limited by the following Examples in which unless otherwise stated :- (i) evaporations were carried out by rotary evaporation in vacuo and work-up procedures were carried out after removal of residual solids by filtration; (ii) operations were carried out at ambient temperature, that is typically in the range 18-26°C and in air unless otherwise stated, or unless the skilled person would otherwise work under an inert atmosphere; (iii) column chromatography (fay the flash procedure) was used to purify compounds and was performed on Merck Kieselgel silica (Art. 9385) unless otherwise stated; (iv) yields are given for illustration only and are not necessarily the maximum attainable; (v) the structure of the end-products of the formula (I) were generally confirmed by NMR and mass spectral techniques [proton magnetic resonance spectra were generally determined in DMSO-d6 unless otherwise stated using a Varian Gemini 2000 spectrometer operating at a field strength of 300 MHz, or a Bruker AM250 spectrometer operating at a field strength of 250 MHz; chemical shifts are reported in parts per million downfield from tetramethysilane as an internal standard (5 scale) and peak multiplicities are shown thus: s, singlet; d, doublet; AB or dd, doublet of doublets; dt, doublet of triplets; dm, doublet of multiplets; t, triplet, m, multiplet; br, broad; fast-atom bombardment (FAB) mass spectral data were generally obtained using a Platform spectrometer (supplied by Micromass) run in electrospray and, where appropriate, either positive ion data or negative ion data were collected]; (vi) intermediates were not generally fully characterised and purity was in general assessed by thin layer chromatographic, infra-red (IR), mass spectral (MS) or NMR analysis; and (vii) in which the following abbreviations may be used :- ® is a Trademark; DMF is N,N-dimeraylformamide; DMA is N,N-dimethylacetamide; TLC is thin layer chromatography; HPLC is high pressure liquid chromatography; MPLC is medium pressure liquid chromatography; DMSO is dimethylsulfoxide; CDC13 is deuterated chloroform; MS is mass spectroscopy; ESP is electrospray; EI is electron impact; CI is chemical ionisation; THF is tetrahydrofuran; TFA is trifluoroacetic acid; NMP is N-methylpyrrolidone; HOBT is 1-hydroxy-benzotriazole; EtOAc is ethyl acetate; MeOH is methanol; phosphoryl is (HO)2-P(0)-0-; phdsphiryl is (HO)2-P~0-; EDC is l-(3-dimemylaminopropyl)-3-ethylcarbodiimide (hydrochloride); PTSA is para-toluenesulfonic acid, (viii) Temperatures are quoted as °C. Sample 1: (5R)-3-(4-fl.4-DioYa-8-a7aspiro[4.5ldec-8-vn-3-flaornphenvn-5-f1.2.3-triazol-lrylmethyl)oxazolJdin-2-one (5J?)-3-(4-(ls4-Dioxa-8-azaspho[4,5]decan-8-yl)-3-fluorophenyl)-5-azidomemyloxazolidin-2-one (2.44 g, 6.5 mM) was dissolved in dioxane (50 ml), treated with nofbornadiene (2,98 g, 32.3 mM) and heated under reflux for 20 hours. After removal of the solvent, the residue was dissolved in dichloromethane (350 ml) washed with water (3 x 200 ml), and dried over magnesium sulfate. After filtration and evaporation the residue was purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 2.5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (1.5 g). MS (ESP): 404 (MET) for C19H22FN5O4 NMR fCDCl,) 8: 1.79 (t,4H); 3.04 (t,4H); 3.80 (dd, 1H); 3.92 (s,4H); 4.04 (t, 1H); 4.70 (m, 2H); 4.96 (m, 1H); 6.85 (overlapping m, 2H); 7.20 (t, 1H); 7.66 (d, 1H); 7.71 (d, 1H). The intermediates for this compound were prepared as follows (see also WO 95-25106 - Ex 3). 4-(1.4-Dioxa-8-azaspiro[4.5]dec-8-yl)-3-fluoronitrobenzene 3,4-DifJuoronitrobenzene (15.53 g, 0.098 M) was dissolved in acetonitrile (150 ml), and treated with -N,N-diisopropylethylamine (31.5 g, 0.244 M) and l,4-dioxa-8-aza- spiro[4,5]decane (15.36 g, 0.107 M). The mixture was stirred and heated to reflux for 18 hours. After cooling, product precipitated as a yellow solid, and was filtered off (16.1 g); further product could be obtained by concentrating the residues (8.43 g). MS (ESPY. 283 (MIT) for CI3H15FN204 NMRfCDCl,) 8: 1.86 (t,4H); 3.41 (t,4H); 4.00 (s,4H); 6.91 (t, 1H); 7.89(dd,lH); 7.96 (dd, 1H). 5- Amino-2-(l .4-dioxa-8-azaspiro[4.5]dec-8-yl)fluorobenzene 4-(l,4-Dioxa-8-azaspiro[4,5]dec-8-yl)-3-fluoronitrobenzene (24.48 g, 0.087 M) was dissolved in ethyl acetate (500 ml) treated with palladium catalyst (10% on carbon, 5 g) and hydrogenated at atmospheric pressure until the theoretical uptake of gas. After filtration through celite and evaporation, the required product was obtained as a pink solid of sufficient quality for use without purification (19.3 g). MS (ESP): 253 (MET) for C13HI7FN202 NMRfDMSO-d£) 8: 1.69 (t,4H); 2.84 (t,4H); 3.86 (s, 4H); 4.91 (s,2H); 6.28 (m,2H); 6.75 (t, 1H). 5-EthoxvcarbonvIammo-2-CL4-dioy:a-8-azaRpiro[4.5]dec-8-vnf1norobenzene 5-Amino-2-(l,4-dioxa-8'azaspiro[4,5]dec-8-yl)£luorobenzene (19.26 g, 0.076 M), was dissolved in dry pyridine (75 ml) and cooled under nitrogen with stirring to 0°. Ethyl chloroformate (9.08, 0.084 M) was added dropwise, and the mixture stirred 30 minutes at the same temperature. Ice-water (300 ml) was added, and stirring continued for 1 hour. The resulting precipitate was collected, washed thoroughly with water, and dried, to give the desired product of sufficient quality for use without purification (20.5 g). MSJCESE): 325 (MH+) for C16H2lFN204 NMRfDMSO-d^ 8: 1.21 (t,3H); 1.71 (t,4H); 2.96 (t, 4H); 3.88 (s,4H); 4.09 (q,2H); 6.95 (t, 1H); 7.09 (dd, 1H); 7.27 (dd, 1H); 9.54 (s, 1H). (5/;)-3-f4-fl.4-Dioxa-8-azaspko[4.5]dec-8-vlV3-fluorophenvlV5-hydroxvrnethv1oyazolidin-2- one 5-Emoxycarbonylamino-2-(l,4-dioxa-8-azaspiro[4,5]dec-8-yl)fluorobenzene (22.9 g, 0.071 M) was dissolved in dry tetrahydrofuran (250 ml) under nitrogen, cooled to -70°, and treated dropwise over 30 minutes with a solution of lithium f-butoxide (1M in tetrahydrofuran, 77.6 ml), keeping the temperature below -70°. After stirring for 5 minutes, (i?)-glycidylbutyrate (11.19 g, 0.077 M) was added, and stirring continued at -65° for 1 hour, before allowing the temperature to rise to ambient over 16 hours. The precipitate was collected and washed with tetrahydrofuran to give the desired product (17.8 g). MS fESPI: 353 (MET) for C17H21FN,05 NMRtoMSO-d^ 8: 1.83 (t, 4H); 3.09 (t, 4H); 3.69 (dd, 1H); 3.82 (dd} 1H); 3.88 (dd, 1H); 3.96 (s, 4H); 4.07 (t, 1H); 4.72 (m, 1H); 4.92 (s, 1H); 7.05 (t, 1H); 7.15 (dd, 1H); 7.46 (dd, 1H). r5ffV3-r4-ri.4-Dioxa-8-azaspiro[4.5]dec-8-v1)-3-f1iioropheTiylV5-Tnethanesulfonyloxvmethvl-r)Yazolidin-2-one [5i2)-3-(4-(l,4-Dioxa-8-azaspko[4,5]dec-8-yl)-3-iluorophenyl)-5-hydroxymethyloxazolidin-2-ane (4.024 g, 11.43 mM) was dissolved in dichloromethane (200 ml), and treated with [riethylamine (1.45 g, 14.4 mM), then cooled under nitrogen to 0°. Methanesulfonyl chloride '1.32 g, 11.5 mM) was added dropwise, and the mixture stirred 18 hours allowing the temperature to rise to ambient. The mixture was washed with water (3 x 75 ml), concentrated, and purified by chromatography on a 90 g silica Biotage column, eluting with 1% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (3.09 g). ! MaiESE):.431(MH+)for C18H23FN207S NMR (DMSO-d) 5: 1.82 (t, 4H); 3.03 (s, 3H); 3.08 (t, 4H); 3.84 (dd, 1H); 3.92 (s, 4H); 4.04 (t, 1H); 4.33 (dd, 1H); 4.43 (dd, 1H); 4.84 (m, 1H); 6.91 (t, 1H); 7.02 (dd, 1H); 7.34 (dd, 1H). (5R)-3-(4-(l14-Dioxa-8-azaspiro[4.5]dec-8-yl)-3-fluorophenyl)-5-azidomethyloxazolidm-2- PJQS (5R)-3-(4-(l,4-Dioxa-8-azaspiro[4,5Jdec-8-yl)-3-fluorophenyl)-5-methanesulfonyIoxymethyl- oxazolidin-2-one (3.03 g, 7.04 mM) was dissolved in N,N-dimemylformamide (50 ml), treated with sodium azide (732 mg, 11.3 mM), and heated with stirring at 50° for 4 hours. After cooling the mixture was diluted with water (250 ml), and extracted into ethyl acetate (3 x 100 ml). The combined organics were dried (magnesium sulfate), and evaporated to give product (2.44 g), of sufficient quality for use without purification. MS (ESP): 378 (MH4) for C]7H2()FN504 NMR (CDCl3) 6: 1.73 (t,4H); 3.02 (t,4H); 3.66 (dd, 1H); 3.74 (m, 2H); 3.91 (s,4H); 4.11 (t, IB); 4.86 (m, 1H); 7.09 (t, 1H); 7.17 (dd, 1H); 7.48 (dd, 1H). Example 2: (5JgV3-r4-f4-Oxopiperidin-l-vn-3-flnorophenyn-5-(1.2.3-triazoM-yImethyI)oxazolidin-2-one (5i?)-3-(4-(l ,4-Dioxa-8-azaspiro[4,5]dec-8-yl)-3-fluorophenyl)-5-(l ,2,3-triazol-l -ylmethyl)oxazolidin-2-one (1.47 g, 3.65 mM) was dissolved in amixture of glacial acetic acid (30 ml) and water (30 ml), and heated at 50° for 18 hours. Solvent was evaporated, the residue azeotroped with toluene (50 ml), then partitioned between ethyl acetate (150 ml) and water (100 ml). The organic layer was washed with saturated aqueous sodium bicarbonate solution (2 x 100 ml), water (100 ml), dried (magnesium sulfate) and evaporated to give product (894 mg), of sufficient quality for use without purification. MS (ESP): 360 (MET) for C17H18FN503 NMR(CDC1^ 8: 2.53 (t, 4H); 3.29 (t, 4H); 3.84 (dd, IH); 4.06 (t, IH); 4.71 (d, 2H); 4.97 (m, IH); 6.90 (overlapping m, 2H); 7.24 (dd, IH); 7.67 (d, IH); 7.72 (d, IH). Example 3: f5J?V3-f4-f4-Aminopiperidui.-1 -vn-3-fluorophenvr>-5-fL2.3-triazo1-1 -ylmeth vnoxazolidin-l-nTi R (5fl)-3-(4-(4-Oxopiperidin-l -yl)-3-fluorophenyl)-5-(l ,2,3-triazol-l -yl) methyl)oxazolidin-2- one (838 mg, 2.33 mM) was dissolved in methanol (25 ml), treated with ammonium acetate (1.8 g, 23.3 mM) and sodium cyanoborohydride (1.03 g, 16.3 mM) and refluxed 16 hours. The mixture was neutralised with 1 N hydrochloric acid, water (125 ml) added, extracted with dichloromethane (5 x 75 ml), and dried (magnesium sulfate). Evaporation gave the desired product (686 mg). MS (ESP): 361 (MH+) for C17H21FN602 NMR rDMSO-d6) 5: 1.43 (m,2H); 1.86(dd,2H); 2.71(tm,4H); 3,29 (m, IH); 3.90 (dd, IH); 4.25 (t, IH); 4.87 (d, 2H); 5.15 (m, IH); 7.08 (t, IH); 7.12 (dd, IH); 7.42 (dd, IH); 7.81 (d, IH); 8.21 (d, IH); NH2 exchanged, not seen. Example 4: f5JgV3-(;4-r4-MethaTiesulfonamidopiperidiii-l-vn-3-flnorophenylV5-ri.2,3" triazoI-l-yImethyI)oxazoIidin-2-one (5if)-3-(4-(4-Aimnopiperidm-l-yl)-3-iluorophenyl)-5-(l,2,3-tria2ol-l-yl)memyl)oxa^^ 2-one (175 mg, 0.49 mM) in dichloromethane (10 ml) was treated with triemylamine (78 mg, 0.78 mM) and methanesulfonyl chloride (67 mg, 0.58 mM) and the mixture stirred for 18 hours at ambient temperature under nitrogen. The niixture was filtered, and solution purified directly by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 2.5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (19 mg). MSJESE): 439(MH+)forC18H23FN604S NMR fDMSO-d^ 8: 1.66 (m,2H); 1.98(dd,2H); 2.76(tm,4H); 3.00 (s, 3H); 3.89 (dd, IH); 4.12 (dd, IH); 4.25 (t, IH); 4.87 (d, 2H); 5.17 (m, IH); 7.08 (t, IH); 7.14 (d, IH); 7.19 (dd, IH); 7.42 (dd, IH); 7.81 (d, IH); 8.21 (d, IH). Example 5: (5R)-3-r4-r4-MethoxycarbonvIaminopiperfdin-l-vn-3-fluorophenvn-f>-ri.2.3-triazo1-l-vlmethynoxazo1idin-2-one (5J2)-3-(4-(4-Aminopiperidin1-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-yl)methyl)oxazolidin 2-one (151 mg, 0.42 mM) in dichloromethane (20 ml) was cooled to 0° and treated with 5% sodium bicarbonate solution (4 ml). The resulting suspension was stirred vigorously, methyl chloroformate (245 mg, 2.6 mM) added, and stirring continued for 3 hours at ambient temperature. The dichloromethane was removed by evaporation, ethyl acetate (15 ml) added, and the organic layer was separated, washed with 2% sodium dihydrogen phosphate (2x15 ml), brine (15 ml), and dried (magnesium sulfate), to give the desired product (170 mg). MSiESE): 419(MHf)forC19H23FN604 NMR (DMSO-d6) 8: 1.53(qm,2H); 1.82(dd,2H); 2.68 (t,2H); 3.24 (m,2H); 3.39 (m, IH); 3.52 (s, 3H); 3.83 (dd, IH); 4.18 (t, IH); 4.83 (d, 2H); 5.09 (m, IH); 7.02 (t, IH); 7.06(dd,lH); 7.15 (d, IH); 7.36(dd,lH); 7.74 (d, IH); 8.14 (d, IH). Example 6: (5JgV3-(4-(4-Methylaminopiperidm-l-yl)->3-flnoropheny][)-5-(1.2.3-triazoI-l" ylmethyl)oxazolidm-2~one (5i2)-3-(4-(4-Oxopiperidm-l-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-ylmemyl)oxazolidm-2-(250 mg, 0.70 mM) was dissolved in a mixture of anhydrous tetrahydrofuran (5 ml) and dichloromethane (5 ml) under nitrogen. Acetic acid (1 drop), methylamine (33% solution in methanol, 31uJL, 0.77 mM) and sodium acetoxyborohydride (222 mg, 1.05 mM) were added, and the mixture stirred at ambient temperature for 3 hours. The mixture was diluted with water (15 ml) and dichloromethane (15 ml), and the pH adjusted to 9 by addition of triemylamine. The organic phase was separated, washed with water (2 x15 ml), brine (15 ml), and dried (magnesium sulfate). Evaporation gave the desired product (145 mg). MS (ESP): 375(MH+)forC18H23FN602 NMRflDMSO-d^ 6: 1.45 (m, 2H); 1.95 (dd, 2H); 2.36 (s, 3H); 2.48 (dd, 2H); 2.71 (t, 2H); 3.91 (dd, IH); 4.25 (t, IH); 4.87 (d, 2H); 5.16 (m, IH); 7.10 (overlapping m, 2H); 7.45 (dd, IH); 7.81 (d, IH); 8.22 (d, IH); NH exchanged, CH-—N under H20, neither seen. Example 7: (5R)-3-(4-(4-Ar-Methy1-niethaDesa1fonamidopiperidiii-1 -v1V3-fluorophenvlV 5-(1.2.3-triazoI-l-ylmethyI)oxazolidm-2-one (5R)-3-(4-(4-Methylammopiperidm-lyi)-3fluorophenyl)-5-(1,2,3-triazol-1yl)methyl)- oxazolidin-2-one (200 mg, 0.53 mM, Example 6), was treated essentially as Example 4 to give the title product after chromatography (53 mg). MS (ESP): 453 (MH+) for C^FNAS NMR(DMSOd6) 8: 1.79 (d,2H); 2.00 (ddd, 2H); 2.74 (t,2H); 2.84 (s,3H); 2.87 (s, 3H); 3.44 (d, 2H); 3.87 (m, IH); 3.89 (dd, IH); 4.12 (t, IH); 4.77 (d, 2H); 5.04 (m, IH); 6.89 (t, IH); 6.95 (dd, IH); 7.28 (dd, IH); 7.74 (d, IH); 7.79 (d, IH). Example 8: (5R))-3-r4-r4-iV-MethyI-methoxycarbonyIaminopiperidm-l-yn-3- fhiorophen vIV5-(l .2.3-triazol-l -vlmeth vnoxazoIidin-2-one (5J2)-3-(4-(4-Methylarnmopiperidin-l-yl)-3-fl^^ oxazolidin-2-one (200 mg, 0.53 mM, Example 6), was treated essentially as Example 4, except for the substitution of methyl chloroformate for methanesulfonyl chloride, to give the title product after chromatography (131 mg). MS(ESP): 433 (MH4) for CjoH^FNA NMRfDMSO-d^ 5: 1.62 (d,2H); 1.82 (ddd, 2H); 2.69 (t,2H); 2.74 (s,3H); 3.32 (d,2H); 3.59 (s, 3H); 3.83 (dd, IH); 3.92 (m, IH); 4.18 (t, IH); 4.81 (d, 2H); 5.10 (m, IH); 7.03 (t, IH); 7.08 (dd, IH); 7.37 (dd, IH); 7.73 (d, IH); 8.13 (d, IH). Example 9: (5igV3 phenyl)-5-(1.23-triazol-l-ylmethyl)oxazolidin"2-one (5i2)-3-(4-(4-Memylanimopiperidm-l-yl)-3-fl^^ oxazolidin-2-one (350 mg, 0.94 mM, Example 6), was treated essentially as Example 4, except for the substitution of acetoxyacetyl chloride for methanesulfonyl chloride, to give the title product after chromatography (207 mg). MS (ESP): 475 (MH4) for C22H27FN605 NMRfDMSO-d.) 8: 1.75 (d,2H); 1.87(dd,2H); 2.07 (s,3H); 2.70 (t,2H); 2.74 (s,3H); 3.36 (d, 2H); 3.62 (m, IH); 3.83 (dd, IH); 4.18 (t, IH); 4.53 (s, 2H); 4.82 (d, 2H); 5.11 (m, IH); 7.10 (overlapping m,2H); 7.49 (dd, IH); 7.76 (d, IH); 8.16 (d, IH). Example 10: (5R) )-3-(4-4-N-MethyNr2-hydro^acetvnami>npfperidm-1-ylV3-fluQrophenvlV5-fl.2.3-triazol-1-vlmethvl1>oxazolidin-2-one (5i?)-3-(4-(4-A^-Methyl-(2-acetoxyacetyl)ammopiperidin 1-yl)-3-fluorophenyl)-5-(l^ triazol-l-ylmethyl)oxazolidin-2-one (186 mg, 0.39 mM) was dissolved in methanol (20 ml), i treated with potassium carbonate (0.3 g, 2.1 mM) and stirred at ambient temperature for 30 minutes, After removal of the solvent the residue was purified by chromatography on a 5 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (30 mg). MS (ESP): 433 (MIT) for C20H25FN6O4 NMRXDMSQdi^ 8: 1.73 (d, 2H); 1.93 (ddd, 2H); 2.74 (t, 2H); 2.79 (s, 3H); 3.45 (d, 2H); 3.68 (s, IH); 3.89 (dd, IH); 4.11 (t, IH); 4.16 (s,2H); 4.58 (m, IH); 4.79 (d,2H); 5.04 (m, IH); 6.91 (t, IH); 6.95 (dd, IH); 7.29 (dd, IH); 7.73 (d, IH); 7.79 (d, IH). Example 11: f5JgV3-r4-r4-(2^-2.3-DihvdroxvpropioiiyI)piperazin-l -yn-3-flttorophenvlV 5-( 1.2.3-triazol-1 -vImefliyl)oxazoIidih-2-one (5i?)-3 NMR fDMSO-d^ 5: 2.91 (brm, 4H); 3.45 (m, IH); 3.51 (m, IH); 3.63 (brm, 4H); 3.82 (dd, IH); 4.18 (t, IH); 4.34 (dd, IH); 4.66 (t, IH); 4.80 (d, 2H); 4.91 (d, IH); 5.11 (m, IH); 7.04 (t5 IH); 7.11 (dd, IH); 7.39 (dd, IH); 7.74 (d, IH); 8.13 (d, IH). The intermediates for this compound were prepared as follows: I. '£> £ifii,.. 4-r4-M^utoxvcarbonylpiperazin-l-ylV3-f]uorophenyl)-5-rL2.3-tria7ol-1-vlmethvnoxazolidiTi-2-nr^R (5i^)-3-(4-(4-^Butoxycarbonylpiperazin4-yl)-3"fluorophenyl)-5-azidomethyl)oxazolidill-2- one (2.52 g, 6 rnM) and norbornadiene (4.2 g, 45.6 mM) were dissolved in dioxane (50 ml) and heated under reflux for 6 hours. After evaporation of solvent, the residue was purified by recrystallisation from isopropanol (50 ml) to give the desired product (2.29 g). MS (ESP): 447(MH^forC21H27FN604 NMR (DMSO-d^ 8: 1.40 (s, 9H); 2.81 (t, 4H); 3.45 (t, 4H); 3.83 (dd, 1H); 4.18 (t, 1H); 4.79 (d,2H); 5.10 (m,lH); 7.06 (t, 1H); 7.11(dd, 1H); 7.38 (dd, 1H); 7.73 (d, 1H); 8.13 (d,lH). (Intermediate oxazoHdinone described in Upjohn WO 93-23384) r5flV3-(;4-(Tiperazin-l-viy3-fluoropheeny)-5-1,2,3-triazol-1-ylmethyl)oxazolidin-2 one (5R)-3 -(4-(4-f-Butoxycarbonylpiperazin-1 -yl)-3-fiuorophenyl)-5-(l ,2,3 -triazol-1 - ylmethyl)oxazolidin-2-one (2.0 g, 4.48 mM), was suspended in ethanol (20 ml), and treated with a solution of hydrogen chloride in ethanol (3.8M, 15 ml). After stirring 18 hours at ambient temperature, the solution was evaporated to dryness, and the residue recrystallised from ethanol and diethyl ether, with charcoal treatment to give the product as its dihydrochloride salt (0.72 g). kl&XESE): 347 (MIT) for C16H19FN602 IVTicroanalvsis: Found, C 46.2; H5.1; N 18.8%. G16H19FN602-2HC1 requires C 45.8; H5.0; Nf20.0% r5^)-3-(4-f4-r(^S)-2.2-Dimemvl-1.3-dioxolane-4-carbonvnpiperazin-1-yn-3-flunrophenyl)-5-[] .2.3 -triazol-1 -vlmethvDoxazoliri jt\|-2-nne Fhe Uthium salt of (4S>2,2-dimemyl-l,3-dioxolan-4-carboxylic acid (342 mg, 2.25 mM) in iichloromethane (10 ml) under nitrogen was cooled with stirring to 0°, treated with thionyl chloride (321 mg, 2.7 mM), then stirred at the same temperature for 3 hours. After filtration, he residue was evaporated to dryness, and redissolved in dichloromethane (10 ml), then tdded to a stirred suspension of (Jif)-3-(4-piperazin-l-yl-3-fluorophenyl)-5-(l,2,3-triazoH-^lmethyl)oxazolidin-2-one dihydrochloride (630 mg, 1.5 mM) in dichloromethane (30 ml) containing pyridine (370 rug, 4.9 mM) and triethylamine (500 mg, 4.9 mM). The mixture was stirred for 18 hours, allowing the temperature to rise to ambient. After dilution with dichloromethane (30 ml), the organic layer was separated, washed with water (3x30 ml), brine (50 ml), and dried (magnesium sulfate). The residue after evaporation was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (278 mg). MS (ESP): 475 (MH) for C22H27FN605 NMRfDMSO-d^) 8: 1.32 (s,6H); 2.95 (br m, 4H); 3.63 (m,4H); 3.86 (dd, 1H); 4.08 (t, 1H); 4.21 (m, 2B); 4.83 (d, 2H); 4.89 (t, 1H); 5.12 (m, 1H); 7.07 (t, 1H); 7.12 (dd, 1H); 7.42 (dd, 1H); 7.77 (d, 1H); 8.17 (d, 1H). Examples 12-16 (5R)-3-(4-(4-(2-Chloroaceryl)piperazin-l-yl)-3-fluorophenyl)-5-(ls2,3-triazol-l-5 ylmethyl)oxazolidin-2-one (422 mg, 1 mM) and the appropriate amine (3 mM) were dissolved in a mixture of dichloromethane (10 ml) and ethanol (1 ml) and stirred at ambient temperature for 18 hours. Solvent was evaporated and the residue purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with an appropriate increasing gradient of methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired i products. Notes 1 MS (ESP^: 474(MH+)for C22H28FN704 NMR(DMSO-d6) 8: 2.40(br,4H); 2.90(br,2H); 2.96(br,2H); 3.19 (br,2H); 3.56 (br, 6H); 3.65 (br, 2H); 3.84 (dd, 1H); 4.20 (t, 1H); 4.83 (d, 2H); 5.12 (m, 1H); 7.06 (t, 1H); 7.11 (dd, 1H); 7.41 (dd, 1H); 7.75 (d, 1H); 8.17 (d, 1H). 2 Sample after chromatography dissolved in the minimum volume of ethanol, treated with a solution of hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether to precipitate the hydrochloride salt. MS (ESP): 462(MH4)for C21 H28FN704 NMRflPMSO-d^ 5: 2.87 (d,3H); 2.99 (brm, 4H); 3.19 (brm, 1EQ; 3.28 (brm, 1H); 3.49 (br, 2H); 3.64 (br, 2H); 3.76 (t, 2H); 3.85 (dd, 1H); 4.18 (t, 1H); 4.34 (dd, 1H); 4.46 (dd, 1H); 4.81 (d, 2H); 5.11 (m, 1H); 7.04 (t, 1H); 7.13 (dd, 1H); 7.40 (dd, 1H); 7.74 (d, 1H); 8.16 (d, 1H); 9.58 (br, 1H); OH missing under solvent; +1H for HC1 salt 3 Little reaction in ethanol at ambient temperature; solvent replaced by isopropanol (10 ml), and refluxed 18 hours before work up as above. Sample after chromatography dissolved in the minimum volume of ethanol, treated with a solution of hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether to precipitate the hydrochloride salt. MS (ESP): 489(MH+)forC22H29FNg04 NMR(DMSO-d^) 5: 1.83 (s, 3H); 2.97 (br, 6H); 3.33 (brm, 2H); 3.51 (br, 2H); 3.64 (br, 2H); 3.85 (dd, 1H); 4.10 (brt, 2H); 4.18 (t, 1H); 4.81 (d, 2H); 5.11 (m, 1H); 7.050 (t, 1H); 7.13 (dd, 1H); 7.41 (dd, 1H); 7.74 (d, 1H); 8.16 (d, 1H); 8.27 (brt, 1H); 9.07 (br, 2H); +1H for HC1 salt. 4 Sample after chromatography dissolved in the minimum volume of ethanol, treated with a solution of hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether ' to precipitate the hydrochloride salt. MS (ESP): 476 (MET) for C22H30FN704 NMR (DMSO-d6) 8: 2.87 (d,3H); 2.99 (m,4H); 3.28 (s, 3H); 3.33 (m, IH); 3.42 (m overlapped by solvent, ~1H); 3.52 (br, 2H); 3.69 (t overlapping br, 4H); 3.86 (dd, IH); 4.20 (t, IH); 4.33 (dd, IH); 4.43 (dd, IH); 4.84 (d, 2H); 5.13 (m, IH); 7.05 (t, IH); 7.13 (dd, IH); 7.42 (dd, IH); 7.75 (d, IH); 8.18 (d, IH); 9.78 (br, IH); +1H for HC1 salt 5 Sample after chromatography dissolved in the minimum volume of ethanol, treated with a solution of hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether to precipitate the hydrochloride salt. MS CESP): 462(MH+)forC21H28FN704 NMRfDMSO-d^ 8: 2.72 (t, 2H); 2.93 (t, 4H); 3.25 (s, 3H); 3.39 (t, 2H); 3.52 (s, 2H); 3.54(br,2H); 3.63(br,2H); 3.84(dd,lH); 4.18 (t, IH); 4.80 (d,2H); 5.11 (m, Iff); 7.03 (t, IH); 7.12 (dd, IH); 7.41 (dd, IH); 7.76 (d, IH); 8.16 (d, IH); NH missing under solvent. The intermediate for these compounds was prepared as follows: (5^-3-r4-(4-pipera7in-l-ylV3-fluorophenvlV5-n ■2.3-triazoU - ylmethvfloxa2olidm-2-one (5jR)-3-(4-(Piperazm-l-yl)-3-iluorophenyl)-5-(1,2,3-triazol-1ylmethyl)oxazolidin-2one dihydrochloride (4.19 g, 10 mM) was suspended in dry dichloromethane (100 ml) under nitrogen and treated with triethylamine (3.03 g, 30 mM) to give a solution. After cooling to 4°, chloroacetyl chloride (1.14 g, 10 mM) was added and the mixture stirred for 15 minutes. The volume was reduced to 20 ml, and the solution chromatographed on silica, eluting with dichloromethane (30 ml). Relevant fractions were combined, washed with water (50 ml) and dried (magnesium sulfate). Evaporation gave the desired product (2.86 g). MS(ESP) - 423 (MIT) for C18H20ClFN6O3 NMR fDMSO-d^ S: 2.93 (br, 2H); 2.98(br,2H); 3.60(br,4H); 3.84(dd,lH); 4.18 (t, IH); 4.41 (s, 2H); 4.81 (d, 2H); 5.11 (m, IH); 7.06 (t, IH); 7.13 (dd, IH); 7.42 (dd, IH); 7.76 (d,lH); 8.16 (d, IH). Example 17: (5RV3-(4-((3R)-3-t-ButoxycarbonvnammopvrroIidin-l-yn-3-fluorn-phenyI)-5-(1.23-triazoM-yImethyfloxazolidin~2-one (5i?)-3-(4-((3i?)-3-(^Butoxycarbonyl)arrmiopyrrolidin-l-yl)-3-fluorophenyl)-5-azidomethyl-oxazolidin-2-one (695 mg, 1.65 mM) was dissolved in dioxane (30 ml), treated with norbornadiene (760 mg, 8.25 mM) and heated under reflux for 6 hours. After removal of the solvent, the residue was dissolved in the minimum of dichloromethane and purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 2.5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (544 mg). MS (ESP): 447 (MH4) for C21H27FN604 NMRfCDCl^ 5: 1.44 (s, 9H); 1.86 (m, IH); 2.24 (m, IH); 3.22 (d, IH); 3.31 (t, IH); 3.52 (m, 2H); 3.84 (dd, IH); 4.04 (t, IH); 4.28 (br, IH); 4.74 (m, 3H); 5.01 (m, IH); 6.58 (t, IH); 6.87 (dd, IH); 7.18 (dd, IH); 7.73 (d, IH); 7.78 (d, IH). The intermediates for this compound were prepared as follows: 3-Fluoro-4-((3R)-3-(t-butoxycarbonyl)aminopyrrohdin-l-yl)mtrobenzene 3,4-Difluoronitrobenzene (16.03 g, 0.101 M) was dissolved in acetonitrile (300 ml), and treated with JVyV-du^opropylemylarnine (32.63 g, 0.253 M) and (3i?)-3-(f-butoxycarbonyl)-aminopyrrolidine (20.65 g, 0.111 M). The mixture was stirred and heated to reflux for 18 hours. Solvent was evaporated, and the residue treated with ethyl acetate (300 ml) and water (200 ml). The organic layer was washed with water (150 ml), citric acid solution (10% in water, 2 x 150 ml), and dried (magnesium sulfate). Evaporation gave the desired product as a yellow solid (32.7 g), of sufficient quality for use without purification. MS (ESP): 326(MH+)forC15H20FN3O4 NMR (CDCl2) 5: 1.43 (s, 9H); 1.85 (m, IH); 2.25 (m, IH); 3.44 (dt, IH); 3.65 (overlapping m, 2H); 3.84 (dm, IH); 4.34 (br m, IH); 4.69 (br, IH); 6.53 (t, IH); 7.87 (dd, IH); 7.92 (dd, IH). 5-Amino-2-((3R)-3-(t-butoxycarbonvl)aminnpyrrolidm-l--yl)fluorobenzene 3-Fluoro-4 was dissolved in ethyl acetate (500 ml) treated with palladium catalyst (10% on carbon, 7.5 g) and hydrogenated at atmospheric pressure until the theoretical uptake of gas. After filtration through celite and evaporation, the required product was obtained as a red gum of sufficient quality for use without purification (29.85 g). MS (ESP): 296 (MH4) for C^PNA NMR rCDC12) 8: 1.44 (s, 9H)l 1-82 (m, 1H); 2.27 (m, 1H); 3.11 (m, 2H); 3.37 (m, 2H); 3.4^,2Hy, 4.27(bim,lHy, 482(br,lHy, 63S(dd,lKy, 6.44 (dd, VKy, 6.57 (t,lH). 5-Ethoxyc3rhnr>Y\|arpiTin-9-((3R-3-(t-butoxycarbonynaminopvn-olidin4-vnf]uoroberi2e 5-Ammo-2-((3R)-3-^butoxycarbonyl)arnmopyrrohdin-l-yl)fluorobenzene (27.33 g, 0.093 M) was dissolved in dry pyridine (150 ml) and cooled under nitrogen with stirring to 0°. Ethyl chloroformate (11.01, 0.102 M) was added dropwise, and the mixture stirred 30 minutes at the same temperature. Ice-water (250 ml) was added, and stirring continued for 1 hour. The resulting precipitate was collected, washed thoroughly with water, and dried, to give the desired product of sufficient quality for use without purification (33.6 g). MS (ESP): 368 (MS") for C18H26FN304 NMRfDMSO-da) 5: 1.21 (t, 3H); 1.36 (s, 9H); 1.90 (m, 1H); 2.05 (m, 1H); 3.04 (m, 1H); 3.20 (m, 1H); 3.32 (m, 1H); 3.40 (m, 1H); 4.02 (br, 1H); 4.05 (q, 2H); 6.62 (t, 1H); 7.02 (d, 1H); 7.08 (d, 1H); 7.22 (d, 1H); 9.38 (br, 1H). (5/?V3'r3-Fluoro-4-rf3igV3-r^butoxvcarbonvl)aminopyrrolidin4-yl)-5-hydroxymethyl- oxazolidin-2-one 5-Emoxycarbonylammo-2-((3jR)-3-(t-butoxycarbon^ (33.6 g, 0.092 M) was dissolved in dry tetrahydrofuran (300 ml) under nitrogen, cooled to -70°, and treated dropwise over 30 minutes with a solution of lithium /-butoxide (1M in tetrahydrofuran, 100.7 ml), keeping the temperature below -65°. After stirring for 5 rninutes, [R)-glycidylbutyrate (14.52 g, 0.101 M) was added, and stirring continued at -65° for 1 hour, jefore allowing the temperature to rise to ambient over 16 hours. The mixture was treated ,vith methanol (50 ml), stirred at ambient temperature for 1 hour, and the precipitate collected md washed well with tetrahydrofuran to give the desired product (21,8 g). VIS fESP): 396 (MH) for C,9H26FN305 3.35 (m, IH); 3.49 (m, 2H); 3.62 (m, IH); 3.73 (dd, IH); 3.98 (t, IH); 4.04 (m, IH); 4.63 (m, IH); 5.15 (t, IH); 6.70 (t, IH); 7.09 (dd overlapping br, 2H); 7.39 (dd, IH). r5igV3-r4-rr3i?V3-(t-butoxvcarbonvDaminopyrrolidm-l-vlV3-fluoropheny1V5- metaanesulfonyloxymethyloxazolidm-2-one (5i?)-3-(4-((5i?)-3-^butoxycarbonyl)ammopyrrolidin^l-yl)-3-fluorophenyl)-5- hydroxymethyloxazolidin-2-one (3.99 g, 10.1 mM) was suspended in dichloromethane (50 ml), and treated with Memylamine (1.53 g, 15.2 mM), then cooled under nitrogen to 0°. Methanesulfonyl chloride (1.39 g, 12.12 mM) was added dropwise, and the mixture stirred 18 hours allowing the temperature to rise to ambient. Precipitated hydrochloride was filtered, the filtrate washed with saturated sodium bicarbonate (75 ml) and water (3 x 75 ml), concentrated, and purified by chromatography on a 90 g silica Biotage column, eluting with dichloromethane. Relevant fractions were combined and evaporated to give desired product (1.25g). MS fESPV 474 (MEt) for C20H28FN3O7S NMRfCDO,) 8: 1.37 (s,9H); 1.82 (m, IH); 2.17 (m, IH); 3.03 (s,3H); 3.17 (d, IH); 3.26 (t, IH); 3.48 (m, 2H); 3.82 (dd, IH); 4.03 (t, IH); 4.24 (br, IH); 4.33 (dd, IH); 4.41 (dd, IH); 4.72 (br, IH); 4.83 (m, IH); 6.57 (t, IH); 6.96 (dd, IH); 7.27 (dd, IH). (5Jg)-3-(4-((3ig)-3-(/-butoxycarbonyl)aminopyrrolidin-1yl)-3-fiurophenyl)-5azidomethyl)- oxazolidin-2-one (5iJ)-3-(4-((3R)-3-(^butoxycarbonyl)ammopyrroUdin-l-yl)-3-fluorophenyl)-5-methane- sulfonyloxymethyloxazohdin-2-one (1.25 g, 2.64 mM) was dissolved in AyV-dimethyl- formamide (20 ml), treated with sodium azide (275 mg, 4.23 mM), and heated with stirring at 50° for 5 hours. After cooling the mixture was diluted with water (100 ml), and extracted into ethyl acetate (3 x 75 ml). The combined organics were dried (magnesium sulfate), and evaporated to give a yellow solid, whichl4:32 was recrystallised from isopropanol to give the required product (715 mg). MS CESV): All (MH) for C19h25fn6o4 NMR(CDC1^ 5: 1.37 (s, 9H); 1.82 (m, IH); 2.17 (m, IH); 3.17 (d, IH); 3.25 (t, IH); 3.51 (dd overlapping m, 3H); 3.61 (dd, IH); 3.71 (dd, IH); 3.95 (t, IH); 4.25 (br, IH); 4.78 (m, 2H); 6.57 (t, IH); 6.98 (dd, IH); 7.28 (dd, IH). Example 18: f5jRV3-r4-rr.?ffV3-AminopvrroIidin-l-yn-3-flnorophenvIV5-fl.2.3-triazo1-l-ylmethyI)oxazolidin-2-one (5^)-3-(4-((3i?)-3"^Butoxycarbonyl)arm^opyiroUdm4-yl)-3-fluorophenyl)-5 NMRfDMSO-dJ 8: 2.03 (m, IH); 2.25 (m, IH); 3.25 (dd, IH); 3.41 (m, IH); 3.51 (m, 2H); 3.82 (overlapping m,2H); 4.17 (t, IH); 4.81 (d,2H); 5.08 (m, IH); 6.74 (t overlapped byH20,~lH); 7.05 (dd, IH); 7.32(dd,lH); 7.74 (d, IH); 8.15 (d, IH); 8.43 (br, ~2H). Example 19: r5J?V3-r4-rr.?/?V3-MethoxycarhonylaminopvrroIidm-l-yIV3-fluorophenvlV 5-(1.2.3-triazol-l-yImethyI)oxazolidin-2-one (5i?)-3-(4-((3i?)-3-AmmopyrroHdm-l-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-yhnethyl)oxazolidin-2-one hydrochloride (200 mg, 0.5 mM) in dichloromethane (20 ml) was cooled to 0° and treated with 5% sodium bicarbonate solution (5 ml). The resulting suspension was stirred vigorously, methyl chloroformate (245 mg, 2.6 mM) added, and stirring continued for 3 hours at ambient temperature. The organic layer was separated, washed with 2% sodium dihydrogen phosphate (2x10 ml), brine (10 ml), and dried (magnesium sulfate), to give the desired product (143 mg). MS (ESP): 405 (MH4) for C18H21FN604 NMR (DMSO-d£> 5: 1.82 (m, IH); 2.11 (m, IH); 3.13 (m, IH); 3.27 (dd, IH); 3.37 (dd, IH); 3.53 (s overlapping m, 4H); 3.81 (dd, IH); 4.09 (m, IH); 4.15 (t, IH); 4.80 (d, 2H); 5.08 (m, IH); 6.69 (t, IH); 7.01 (dd, IH); 7.28 (dd, IH); 7.42 (br, IH); 7.75 (d, IH); 8.13 (d, IH). Example 20: r5/gV3^4-rf3RV3-rf4SV2.2-dimethvI-1.3-dioxolan-4-yImethoxy- carbonylammo)pyrrolidin-l-yI)-3-fluorophenyIV5-ri.2.3-ti,iazoI-l-ylmethyI)oxazolidin- 2-one (J29-3-(4-((3/0-3-Ainmopym)H^ oxazolidin-2-one hydrochloride (400 mg, 1.05 mM) was suspended in tetrahydroiuran (10 ml) and treated with du^opropylethylarnine (176 mg, 1.36 mM) and (4S)-2,2-dimethyl-l,3- dioxolan-4-ylmethyl 4-nitrophenyl carbonate (429 mg, 1.44 mM) dissolved in dichloromethane (5 ml). The mixture was stirred vigorously at ambient temperature for 18 hours, with the addition of two further portions of dusopropylemylarnine (137 mg, 1.06 mM). Solvent was evaporated, the residue redissolved in ethyl acetate (20 ml), washed with water (3 x 20 ml), and dried (magnesium sulfate). After removal of the solvent, the residue was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (273 mg). MS fESP;>: 505 (MH) for (yEWNA NMRfDMSO-d^ 5: 1.25 (s,3H); 1.31 (s, 3H); 1.84 (m, 1H); 2.10 (m, 1H); 3.15 (m, 1H); 3.38 (dd, 1H); 3.50 (t, 1H); 3.63 (t, 1H); 3.81 (dd, 1H); 3.91 (m, 1H); 3.95-4.25 f (overlapping m, 6H); 4.79 (d, 2H); 5.08 (m, 1H); 6.69 (t, 1H); 7.01 (dd, 1H); 7.28 (dd, 1H); 7.57 (br, 1H); 7.75 (d, 1H); 8.14 (d, 1H). The reagent for this compound was prepared as follows: (4SV2.2-DimethyM.3-dioxolan-4-ylmethyl 4-nitrophenyl carbonate (^iS)-2,2-Dimethyl-l,3-dioxolan-4-ylmethanol (362 mg, 2.74 mM) was dissolved in pyridine (9 ml), stirred at ambient temperature, and treated in portions with 4-nitrophenyl chloroformate (552 mg, 2.74 mM). After 6 hours, solvent was evaporated, the residue redissolved in ethyl acetate (15 ml), washed with water (15 ml), sodium bicarbonate solution (15 ml), brine (15 ml), and dried (magnesium sulfate). Removal of the solvent gave the product as an oil sufficiently pure for further use (858 mg). MS ffiSP): 298 (MH) for C13HlfN07 NMR fDMSO-d^ 6: 1.28 (s,3H); 1.34 (s,3H); 3.74(dd,lH); 4.05 (t, 1H); 4.20 (dd, 1H); 4.25(dd,2H); 7.54 (d,2H); 8.29 (d,2H). Example 21: f5JgV3-f4-(f3J?V^-rf2SV2.3-DihydroxvpropvIo3cvcarbonyIamino^pyrrolidin-l-yl)-3-flttorophenyl)-5-fl.2.3-triazol-l-yImethyl)oxazolidin-2-one yI)-3-fluorophenyl)-5-(l,2,3-Mazol-l-ylmethyl)oxazolidin-2-one (240 mg, 0.48 mM) in tetrahydrofuran (5 ml) was treated with hydrochloric acid (2M, 2 ml) and stirred at ambient temperature for 18 hours. Solid potassium carbonate was added to neutralise, and the mixture filtered, and the filtrate evaporated to dryness. The residue was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 10% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (170 mg). MS (ESP): 465 (MH+) for C^FNA NMR (DMSO-d^ 8: 1.83 (hextet, IH); 2.10 (hextet, IH); 3.15 (s, IH); 3.17 (s, IH); 3.33 (t, 2H); 3.50 (t, IH); 3.60 (dd, IH); 3.80 (dd, IH); 3.84 (dd, IH); 3.97 (dd, IH); 4.05 (dd, IH); 4.09 (d, IH); 4.15 (t, IH); 4.54 (t, IH); 4.73 (d, IH); 4.80 (d, 2H); 5.08 (m, IH); 6.69 (t, IH); 7.00 (dd, IH); 7.27 (dd, IH); 7.43 (d, IH); 7.74 (d, IH); 8.13 (d, IH). Example 22: r5/gV3-f4-ff3JeV3-(2-Methoxvetlioxvcarbonvlaniinn^pyrrolidin-l-yn-3-fluoropheny1)-5-fl.2.3-triazoI~l-ylmethyl)oxazolidiii-2-one (Ji?)-3 oxazolidin-2-one hydrochloride (200 mg, 0.52 mM) was suspended by stirring in dichloromethane (10 ml) at 0° and sodium bicarbonate solution (5 ml) added. 2-Methoxyethyl chloroformate (340 mg, 2.46 mM) was added, and the mixture stirred 4 hours, allowing the temperature to rise to ambient. The organic layer was separated, washed with sodium dihydrogen phosphate (2%, 2x15 ml), water (15 ml) and dried (magnesium sulfate). Filtration and evaporation gave the desired product (183 mg). MS flESP^: 449 (MH^) for QoH^FNA NMRfDMSO-d^ 8: 1.82 (hextet, IH); 2.10 (hextet, IH); 3.13 (m, IH); 3.24 (s,3H); 3.36 (t, IH); 3.48 (m, 4H); 3.79 (dd, IH); 4.05 (m, 3H); 4.16 (t, IH); 4.79 (d, 2H); 5.08 (m, IH); 6.69 (t, IH); 7.01 (dd, IH); 7.28 (dd, IH); 7.51 (d, IH); 7.74 (d, IH); 8.13 (d, IH). Example 23: (5R)V3-r4-rr3JgV3-f2-Hydroxyethoxycarbonylamino^pyrrolidiii-l-yn-3-flnorophenyIl-5-(L2.3-triazoI-t-yImethyI)oyazoIidm-2-one The resin bearing the title compound bound via its terminal hydroxy group (200 mg, nominz 0.118 mM) was swelled in dichloromethane (2 ml) for 30 minutes. Excess solvent was drained, and a solution of trifluoroacetic acid (1% in dichloromethane, 1 ml) was added, and the mixture agitated at ambient temperature for 2 hours. The resin was washed repeatedly with dichloromethane (5x5 ml), and the combined washings concentrated. The gum so obtained was azeotroped with isohexane/dichloromethane (20 ml) to give the desired produc (40 mg). MS (ESP): 435 (MET) for C19H23FN605 NMRfDMSO-d^ 5: 1.85 (hextet, 1H); 2.10 (hextet, 1H); 3.17 (m, 1H); 3.28 (dd, 1H); 3.41 (dd, 1H); 3.51 (m, 2H); 3.82 (dd, 1H); 3.97 (t, 1H); 4.12 (m, 1H); 4.17 (t, 1H); 4.29 (m, 1H); 4.55 (m, 1H); 4.81 (d, 2H); 5.10 (m, 1H); 6.69 (t, 1H); 7.01 (dd, 1H); 7.27 (dd, 1H); 7.46 (d, 1H); 7.75 (d, 1H); 8.15 (d, 1H); 1 x OH exchanging, not seen. The intermediates for this compound were prepared as follows: A polystyrene resin derivatised with 2-hydroxyethoxy-2'-chlorotrityl functionality (Novabiochem, 0.59 mM/g, 250 mg, 0.148 mM) was swelled in base-washed dichloro¬methane (3 ml) for 30 minutes, then excess dichloromethane drained. A solution of 4-nitrophenyl chloroformate (149 mg, 0.738 mM) and pyridine (175 mg, 2.22 mM) in base-washed dichloromethane was added, and the mixture shaken gently for 18 hours at ambient temperature. Solvent was then drained, and the resin washed with several portions of dichloromethane, then diethyl ether and dried in a desiccator. IR: 1768; 1596; 1264 cm'1. The above resin (200 mg, nominally 0.118 mM) was swelled miV^-dimethylacetamide (3 ml) for 30 minutes, solvent drained, and a pre-mixed solution of (5i?)-3-(4-((3i?)-3-ammopyrroHo%-l-yl)-3-fiuorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxa2oUdm-2-one hydrochloride (226 mg, 0.59 mM) and dnsopropylethylamine (228 mg, 1.77 mM) in AyV"-dimethylacetamide (3 ml) added. The mixture was shaken gently for 4 hours at ambient temperature. Solvent was then drained, and the resin washed with 7^-dimethylacetamide (3 x 4 ml), then dichloromethane (3x4 ml), and dried in a desiccator: IE: 3409; 1758; 1725 compound"1. Example 24: (5R)3-f4-((3S-3-(t-BntoTvcarhonvnaniinopvrroIidin-l-ylV3-fluoro~ phenyl)-5-(1.2.3-triazol-l-ylmethyI)oxazoIidm-2-one (5i2)-3-(4-((5iS)-3-^Butoxycarbonyl)ammopyrroUdin-l-yl)-3-fluorophenyl)-5-azidomethyl-oxazolidin-2-one (3.2 g, 7.61 mM) was reacted by essentially the technique of Example 17 and purified by chromatography on a 60 g silica Biotage column, eluting with a gradient increasing in polarity from 0 to 7% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (1.66 g). MS (ESVY. 447 (MH4) for Q^FNA NMR fDMSO-d^ 6: 1.39 (s, 9H); 1.84 (m, IH); 2.10 (m, IH); 3.12 (m, IH); 3.27 (t, IH); 3.38 (m, IH); 3.50 (t, IH); 3.83 (dd, IH); 4.06 (m, IH); 4.18 (t, IH); 4.82 (d, 2H); 5.11 (m, IH); 6.71 (t, IH); 7.03 (dd, IH); 7.13 (br, IH); 7. 30 (dd, IH); 7.77 (d, IH); 8.16 (d, IH). The intermediates for this compound were prepared as follows: 3-Fluoro-4-rri^-3-r^bntoxycarbony^aminopviTolidin-l-yDnitrobenzene Using essentially the technique for the equivalent intermediate in Example 17, but starting from (5iS)r3-(^butoxycarbony)laminopyrroUdine (20 g, 0.108 M), gave the desired product as a yellow solid (33.5 g), of sufficient quality for use without purification. MS fESP): 326 (MH4) for C15H20FN3O4 NMR fDMSO-ayi 5: 1.36 (s,9H); 1.87 (m, IH); 2.08 (m, IH); 3.36 (m, IH); 3.54 (m, IH); 3.62 (tm, IH); 3.73 (m, IH); 4.09 (m, IH); 6.72 (t, IH); 7.19 (d, IH); 7.88 (overlapping m, 2H). 5-Anu^o-2-((3^-3-r^butoxvcarbonvnaminopyrrolidm-1-yl)fluorobenzene Using essentially the technique for the equivalent intermediate in Example 17, but starting from S-fluoro^-^i^-S-^butoxycarbony^ammopyrroUdm-l-y^nitrobenzene (33.5 g, 0.103 M), gave the desired product as an oil of sufficient quality for use without purification (-30 5-Ethoxycarbonylammo-2-((3iS)-3-(^b^ (35.2 g, 0.096 M). was dissolved in dry tetrahydrofuran (400 ml) under nitrogen, cooled to -70°, and treated dropwise over 20 minutes with a solution of lithium f-butoxide, prepared from f-butanol (9.3 g, 123 mM) in dry tetrahydrofuran (70 ml) and n-butyl lithium (66 ml, 1.6M in hexane). After stirring for 20 minutes, (i?)-glycidylbutyrate (15.2 g, 0.102 M) in tetrahydrofuran (20 ml) was added over 10 minutes, and the temperature allowed to rise to ambient over 16 hours. The mixture was treated with methanol (10 ml), stirred at ambient temperature for 10 minutes, then treated with a mixture of 5% aqueous sodium bicarbonate (250 ml) and ethyl acetate (500 ml). The precipitate was collected and washed well with ethyl acetate and water to give the desired product (19.5 g). The filtrate was separated into an organic layer, which was dried (magnesium sulfate) and evaporated The residue was refluxed briefly with ethyl acetate (100 ml), cooled, and filtered to give further product (16.6 MS (TBSP): 396 (MB4) for C19H26FN305 NMR (DMSO-d^ 5: 1.37 (s, 9H); 1.79 (m, 1H); 2.07 (m, IK); 3.08 (m, 1H); 3.24 (m overlapping H20, ~1H); 3.36 (m, 1H); 3.48 (tm, 1H); 3.53 (d, 1H); 3.63 (d, 1H); 3.74 (dd, 1H); 3.99 (t, 1H); 4.04 (m, IK); 4.63 (m, 1H); 5.15 (s, 1H); 6.71 (t, 1H); 7.08 (dd over¬lapping br, 2H); 7.39 (dd, 1H). r5i?V3-(4-((3^-3-(^Butoxycarbonyl)anunopyiToHdm-l-ylV3-fluorophenyl)-5-methane-sulfonyloxymethyloxazQlidin-2-one (5J2)-3-(4-((56)-3-^Butoxycarbonyl)anrniopyrroUdm-l-yl)-3-fluorophenyl)-5-hydroxy-methyloxazolidin-2-one (3.04 g, 7.7 mM) was suspended in a mixture of dichloromethane (25 ml) and pyridine (20 ml), cooled under nitrogen to 0°, and treated with triethylamine (1.15 g, 11.4 mM). Methanesulfonyl chloride (1.04 g, 9.1 mM) in dichloromethane (5 ml) was added dropwise, and the mixture stirred 45 minutes at the same temperature. The mixture was concentrated to dryness, and the residue dissolved in ethyl acetate (70 ml), then washed with 5% sodium bicarbonate (70 ml), water (2 x 70 ml), brine (70 ml), and dried (magnesium sulfate). After evaporation and azeotroping with toluene (20 ml), product of sufficient quality was obtained for use without further purification (3.64 g). MS rESP): 474 (MB4) for C2DH28FN307S NMR rPMRO-d^ 5: 1.37 (s, 9H); 1.81 (m, 1H); 2.08 (m, 1H); 3.11 (m, 1H); 3.26 (s, 3H); 3.28 (m, 1H); 3.38 (m, IK); 3.49 (tm, IK); 3.76 (dd, 1H); 4.05 (m, IK); 4.11 (t, 1H); 4.43 (dd, IK); 4.50 (dd, IK); 4.96 (m, IK); 6.72 (t, IK); 7.10 (dd, IK); 7.16 (d, IK); 7.49 (dd, IK). f5igV3-r4-r^^-3~^Buto\^carbonvnaminopvrrolidin4-v1V3-fluoropheny1V5-azidomethvl-oxazolidin-2-one (5i?)-3-(4-((3iS)-3-(^Butoxycarbonyl)arxitnopyrrohdm-l-yl)-3-fluorophenyl)-5-methane-sulfonyloxymethyloxazolidin-2-one (3.6 g, 7.61 mM) was dissolved in A^V'-dimethyl-formamide (40 ml), treated with sodium azide (0.99 g, 15.2 mM), and heated with stirring at 80° for 3.5 hours. After cooling the mixture was diluted with water (400 ml), and extracted into ethyl acetate (400 ml). The combined organics were washed with water (2 x 400 ml) and brine (200 ml), dried (magnesium sulfate), and evaporated to give the required product (3.2 g)- MS (ESP): 421 (MH) for C19H25FN604 Example 25: f5J?V3-r4-fr3^-3-AminopyrroIidiii-l-vn-3-fluorophenylV5-a.2.3-triazo1-l-ylmethyl)oxazoIidm-2-one (5i?)-3-(4-((itf)-3-^Butoxycarbonyl)a l-ylmethyl)oxazolidin-2-one (1.55 g, 3.47 mM), was dissolved in dichloromethane (8 ml), and treated with a solution of hydrogen chloride in ethanol (3.8M, 40 ml). After stirring 2 hours at ambient temperature, the mixture was evaporated to dryness to give product as a hydrochloride of sufficient quality to require no purification (1.64 g). MS (ESP): 347 (MET) for C16H19FN602 NMRfl3MSO-df) 6: 2.00 (m, IH); 2.25 (m, IH); 3.24 (dd, IH); 3.41 (m, IH); 3.52 (m, 2H); 3.82 (overlapping m,2H); 4.17 (t, IH); 4.81 (d,2H); 5.10 (m, IH); 6.78 (t, IH); 7.06 (dd, IH); 7.33 (dd, IH); 7.76 (d, IH); 8.17 (d, IH); 8.36 (br, ~2H). Example 26: r5J?V3-r4-fr^-3-AcetamidopyrroIidin-l-yn-3>flnorophenvn-5-f 1.2.3-triazol-l-ylmethyl)oxazolidip-2-one Using essentially the technique of Example 19, but starting from (5iZ)-3-(4-((55)-3-ammopyiroHdm-l-yl)-3-fluorophenyl)-5-(l,2,3-1riazol-l-ylmemyl)oxazoUdin-2-one hydrochloride (250 mg, 0.65 mM), and replacing the methyl chloroformate with acetic anhydride gave the desired product (150 mg). MS (ESP): 405 (MET) for C18H21FN603 NMR fDMSO-d,) S: 1.87 (s overlapping m, 4H); 2.16 (m, IH); 3.18 (m, IH); 3.33 (dd, IH); 3.46 (t, IH); 3.56 (tm, IH); 3.88 (dd, IH); 4.24 (t, IH); 4.35 (m, IH); 4.88 (d, 2H); 5.15 (m,lH); 6.89 (t, IH); 7.08 (dd, IH); 7.37 (dd, IH); 7.84 (d, IH); 8.19 (d, IH); 8.23 [d, IH). Using essentially the technique of Example 19, but starting from (5if)-3-(4-((55)-3- ammopyrroh^n-l-yl)-3-fiuorophenyl)-5-(l,2,3-M hydrochloride (250 mg, 0.65 mM) gave the desired product (192 mg). MS (ESP): 405 (MET) for ClgH21FN604 NMR fDMSO-d£) 5: 1.82 (m, 1H); 2.11 (m, 1H); 3.13 (m, 1H); 3.31 (m overlapping H20, ~2H); 3.51 (s overlappingm, 4H); 3.81 (dd, 1H); 4.07 (m, 1H); 4.17 (t, 1H); 4.80 (d, 2H); 5.08 (m, 1H); 6.71 (t, 1H); 7.02 (dd, 1H); 7.27 (dd, 1H); 7.47 (d, 1H); 7.76 (d, 1H); 8.15 (d, 1H). Example 28: (5Jg)-3-f4-rf.?,V)-3-Methanesulfonamidopvrro]idin-l-vlV3-fli]nrophenvTV5-(1.2.3-triazol-l -yImethyl)oxazolidin-2-one (5J?)-3 MS (ESP): 425 (MH4) for C17H21FN60 NMR fDMSO-dJ 8: 1.84 (m, 1H); 2.18 (m, 1H); 2.93 (s, 3H); 3.18 (m, 1H); 3.34 (m overlapping H20,~2H); 3.54 (t, 1H); 3.80 (dd, 1H); 3.96(dd,lH); 4.15 (t, 1H); 4.49 (d, 2H); 5.08 (m, 1H); 6.71 (t, 1H); 7.01 (dd, 1H); 7.28 (dd, 1H); 7.34 (d, 1H); 7.74 (d, 1H); 8.13 (d, 1H). EmmDle29: (SjR)^-r4-Tmidazoi-l-vI-3-fluoroiyhenvl).5-n.2.3-triazol-l-vlmethyl)-oxazolidin-2-one (5i?)-3-(4-Imidazol-l-yl-3-fluoroplienyl)-5-a2idomethyloxazolidiii-2-one (755 mg, 1.35 rnM) was dissolved in dioxane (40 ml), treated with norbornadiene (1.15 g, 12.5 mM) and heated under reflux for 16 hours. After removal of the solvent, the residue was dissolved in the minimum of dichloromethane and purified by chromatography on a 20 g silica Mega Bond • Elut® column, eluting with a gradient increasing in polarity from 0 to 10% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (660 mg). MS (PSg): 329 (MIT) for C15H13FN602 NMRiRMSQ^ 8: 3.95 (dd, 1H); 4.29 (t, 1H); 4.85 (d, 2H); 5.16 (m, 1H); 7.11 (d, 1H); 7.39 (dd, 1H); 7.54 (overlapping m, 2H); 7.66 (d, 1H); 7.77 (d, 1H); 7.98 (m, 1H); 8.18 (d, 1H). (Intermediate oxazolidinone described in Upjohn WO 96-23788) Example30: f5K)-3-(4-ImidazoI-1 -vl-3-fluorophenvn~5-fl-pviazoIyl)methyI)oxazoIidin-?-one Sodium hydride (60% in oil, 32 mg, 0.8 mM) was stirred under nitrogen in A^AT-dirnethylformamide (2 ml), pyrazole (68 mg, 1 mM) added, and stirring continued for 10 minutes. (5R)-3 -(4-hnidazoM -yl-3-fluorophenyl)-5-methanesiifonyloxymethyloxazolidin-2-one (142 mg, 0.4 mM) was dissolved in iV^-dimethylformarnide (1 ml) added to the above, and the mixture stirred 18 hours at ambient temperature. After diluting with 5% aqueous sodium bicarbonate (30 ml), the mixture was extracted with ethyl acetate (50 ml), the extract cashed with water (2x 30 ml), brine (25 ml), dried (magnesium sulfate) and evaporated. The residue was dissolved in the rninirmiTn of dichloromethane and purified by chromatography on i 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 ;o 15% isopropanol in dichloromethane. Relevant fractions were combined and evaporated, hen dissolved in dichloromethane (5 ml) and stirred for 18 hours with PS-Isocyanate resin Argonaut Technologies, 500 mg) to remove ring opened impurities. Filtration and ivaporation gave the desired product (34 mg). v£S (ESP.): .328 (Mir) for C16HI4FNA NMRtpMSO-dJ 8: 3.89 (dd, 1H); 4.17 (t, 1H); 4.46 (d, 2H); 5.04 (m, 1H); 6.21 (t, 1H); 7.08 (m, 1H); 7.32 (dd, 1H); 7.39 (d, 1H); 7.50 (m, 1H); 7.58 (t, 1H); 7.60 (dd, 1H); 7.72 ' (d, 1H); 8.00 (m, 1H). (Intermediate described in WO 96-23788) Example 31: (5ig)-3-(4-Imidazol-l-yl-3-fluorophenyl)-5-tetrazoI-l-ylmethyloxazolidm-2-oneand(5R)-3-(4-ImidazoI-l-yl-3-fluoropheny))-5-tetrazoI-2-ylmethyloxazoIidm-2-ope (5J?)-3-(4-Inn^azol-l-yl-3-fluorophenyl)-5-memanesulfonyloxymemyloxazoUdm mg, 0.7 mM) was dissolved in A^A^dimethylformamide (2 ml), treated with li7-tetrazole (123 mg, 1.75 mM) and potassium carbonate (241 mg, 1.75 mM), and heated at 95° for 3 hours. After cooling, the mixture was diluted with water (30 ml), extracted with ethyl acetate (50 ml), the extract washed with water (2x 30 ml), brine (25 ml), dried (magnesium sulfate) and evaporated. The residue was dissolved in the minimum of dichloromethane and purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 10% isopropanol in dichloromethane, then 0 to 20% methanol in dichloromethane. Relevant fractions were combined and evaporated, the first eluting product being the 2-isomer (80 mg). MS (ESP): 330(MH+)forC14H12FN7O2 NMR (DMSO-dg) 8: 3.96(dd,lH); 4.34 (t,lH); 5.26 (overlapping m, 3H); 7.12 (m, IB); 7.40 (dd, 1H); 7.55 (d, 1H); 7.66 (t overlapping dd, 2H); 8.00 (m, 1H); 9.05 (s, 1H). The second eluting product was the 1-isomer (51 mg). MS (ESP): 330(MB+)forC14H12FN7O2 NMR rDMSO-d^ 8: 3.98 (dd, 1H); 4.31 (t, 1H); 4.95 (m, 2H); 5.21 (m, 1H); 7.12 (m, IB); 7.43 (dd, 1H); 7.55 (d, IB); 7.67 (t overlapping dd, 2H); 8.01 (m, 1H); 9.49 (s, 1H). Intermediate described in WO 96-23788. Example 32: f5ift-3-(4-f4-HvdroxymethvIimidazoM -vn-3-fluorophenvlV5-tetrazoI-l- ^lmethyIoxazoIidin-2-oneand(5RV3-(,4-r4-Hydroxymethylimidazol-l-yl)-3- nuorophenyIV5-tetrazol-2-yImethyIoxazoIidin-2-one '5if)-3-(4-(4-^Buryldmiemylsilyloxymemyh^mdazol-l-yl)-3-fluorophenyl)-5-hydroxy-nemyloxazolidin-2-one (421 mg, 1 mM), l#-tetrazole (105 mg, 1.5 mM), and triphenyl- phosphine (393 mg, 1.5 mM) were dissolved by stirring in dry tetrahydrofuran (5 ml) under nitrogen in an ice-bath. Diisopropylazodicarboxylate (303 mg, 1.5 mM) was added dropwise, and the mixture stirred 2 hours, allowing the temperature to rise to ambient. The mixture was cooled to 0°, treated with trifluoroacetic acid (5 ml), and stirred 30 rninutes at ambient temperature. The mixture was diluted with ethyl acetate (100 ml), and extracted with aqueous hydrochloric acid (1M, 100 ml). The acid extract was washed with ethyl acetate (100 ml), then made basic with concentrated aqueous ammonia, and reextracted with dichloromethane. After drying (magnesium sulfate), the residue was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 10% methanol in dichloromethane. Relevant fractions were combined to give the less polar tetrazol-2-yl isomer (105 mg). MS fESP^l: 360 0vnr)forC15H,4FN7O3 NMRfDMSO-dg) 8: 3.96 (dd, 1H); 4.32 (t, 1H); 4.39 (d, 2H); 4.96 (t, 1H); 5.16 (dd, 1H); 5.25 (dd, 1H); 5.31 (m, 1H); 7.32 (d, 1H); 7.38 (dd, 1H); 7.63 (t, 1H); 7.66 (dd, 1H); 7.90 (d, 1H); 9.02 (s, 1H). The aqueous ammonia liquors were cooled to 4° overnight, to precipitate crystals of the more polar tetrazol-1 -yl isomer (6 mg). MS (ESPV 360 (MIT) for C14H12FN702 The oxazolidinone intermediate is described in WO 97-31917. Example33: f5Jfl-3-f4-f2-MethvlimidazoM-vn-3-fliiorophenvr>-5-tetrazol-1 -vl- methyIoxazolidm-2-oneand(5i?V3-r4-r2-Methylimidazol-l-yI)-3-flaorophenyI)-5- tetrazol-2-yImethyIoxazoIidm-2-one Essentially the technique of Example 17 was used, but starting from (5i?)-3-(4-(2-memylimidazol-l-yl)-3-fluorophenyl)-5-hydroxymethyloxazoUdin-2-one (582 mg, 2 mM). Crude material from the acid extract was purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 20% methanol in dichloromethane. Relevant fractions of the first eluting product were combined to give the less polar tetrazol-2-yl isomer (246 mg). MS fESP): 344 (MIT) for CI5H14FN702 NMR fDMSO-d^ 5: 2.14 (s, 3H); 3.97 (dd, 1H); 4.34 (t, 1H); 5.16 (dd, 1H); 5.26 (dd, IH); 5.32 (m, IH); 6.91 (d, IK); 7.20 (d, IK); 7.40 (dd, IH); 7.54 (t, IK); 7.66 (dd, 1H); 9.02 (sa IH). The second eluting product was the 1-isomer (210 mg). MSilSE): 344 (MET) for C15H14FN702 NMR (DMSO-d^ 8: 2.13 (s, 3H); 3.97 (dd, IH); 4.31 (t, IH); 4.94 (d, 2H); 5.21 (m, IH); 6.91 (d, IH); 7.20 (d, IH); 7.42 (dd, IH); 7.55 (t, IH); 7.67 (dd, IH); 9.47 (s} IH). The intermediates for these compounds were prepared as follows: 3-Fluorn-4~(2-methylimidazol-]["yl)nitrobenzene 2-Methylimidazole (9.02 g, 0.11 M) and N,N-diisopropylemylarnine (32.2 g, 0.25 M) were dissolved in acetonitrile (160 ml), and 3,4-difluoromtrobenzene (15.9 g, 0.1 M) added. The mixture was stirred and heated to reflux under nitrogen for 24 hours. Solvent was evaporated, the residue dissolved in ethyl acetate (300 ml), washed with water (150 ml), brine (150 ml), and dried (magnesium sulfate). The residue was recrystallised from a mixture of ethyl acetate (25 ml) and cyclohexane (150 ml) with the addition of charcoal to give the title compound (11.5 g),mp 106-107°. M3_Q3£E): 222 (MH1) for C10HgFN3O2 NMR fDMSO-d_;> 6: 2.25 (s, 3H); 7.00 (d, IH); 7.35 (t, IH); 7.87 (t, IH); 8.23 (dd, IH); 8.43 (dd, IH). 5-Amino-2-(2-methylimidazol-l-vnfluorobenzene 3-Fluoro-4-(2-methylimidazol-l-yl)nitrobenzene (40 g, 0.181 M) was dissolved in a mixture of methanol (200 ml) and tetrahydrofuran (800 ml), cooled to 0° under nitrogen, and treated with ammonium formate (57 g, 0.905 M) followed by palladium on charcoal (10%, 2 g). The mixture was stirred at ambient temperature for 18 hours, filtered through celite, celite washed with methanol (100 ml), and filtrate evaporated to dryness. The residue was partitioned between ethyl acetate (800 ml) and 10% aqueous sodium bicarbonate (250 ml). The organic layer was separated, washed with brine (250 ml), dried (magnesium sulfate) and evaporated to give title compound (34.6 g). _MS flESP): 192 (MH) for C10H10FN3 NMR CPMSO-dJ 5: 2.08 (s, 3H); 5.68 (s, 2H); 6.45 (overlapping m, 2H); 6.84 (d, 1H); 7.03 (overlapping m, 2H). 5-Benzvloxvcarhonylamino-2-r2-methvlimidazol-l-yDfluorobenzene 5-Arrmio-2-(2-memylimidazol-l-yl)fluorobenzene (34.25 g, 0.179 M) was dissolved in dry dichloromethane (600 ml) under nitrogen, and cooled to -5°. Pyridine (17.7 g, 0.224 M) was added, followed by benzyl chloroformate (33.7 g, 0.197 M) over 20 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 250 ml) was added, the organic layer separated, the aqueous layer re-extracted with dichloromethane (2 x 300 ml), and combined extracts dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (400 ml) to give title product (54.5 g). MS^ESE): 326(MH+)forC18H16FN302 NMRfDMSO-d^ S: 2.13 (s, 3H); 5.18 (s, 2H); 6.89 (s, 1H); 7.17 (s, 1H); 7.41 (overlapping m, 7H); 7.73 (dd, 1H); 10.21 (br, 1H). (5Jg)-3-(3-Fluoro-4-(2-methylmiida7.ol-l-yl)phenylV5-hydroxymethyloxazolidin-2-one 5-Benzyloxycarbonylammo-2-(2-methylimidazol-l-yl)fluorobenzene (54 g, 0.166 M) was dissolved in a mixture of dry tetrahydrofuran (600 ml) and 1,3-dimethyl-tetrahydropyrirnidin-2-one (100 ml) under nitrogen, cooled to -70°, and treated with a solution of n-butyllithium (1.6M in isohexane, 1.14 ml), over 30 minutes. After stirring for 30 minutes at -70°, a solution of (iO-glycidylbutyrate (26.35 g, 0.183 M) in dry tetrahydrofuran (50 ml) was added over 15 minutes. Stirring was continued for 16 hours allowing the temperature to rise to ambient. The mixture was treated with aqueous sodium bicarbonate (5%, 500 ml) and ethyl acetate (800 ml), the organic layer separated, and the aqueous extracted with further ethyl acetate (3 x 750 ml). The combined extracts were dried (magnesium sulfate) and evaporated, and the resulting oil triturated with diethyl ether. The resulting solid was recrystallisd from isopropanol to give the title compound (21.5 g). MS (ESP): 292 (MH4) for C, jvrivQlfDMSO-d^ S: 2.16 (s,3H); 3.56 (dt, 1H); 3.69 (dt, 1H); 3.88 (dd, 1H); 4.15 (t,lH); 4.74 (m, 1H); 5.24 (t, 1H); 6.92 (s, 1H); 7.20 (s, 1H); 7.48 (dd, 1H); 7.53 (t, 1H); 7.74 (dd, 1H). Example 34: (5JgV.^-f4-f4-Methylimidazol-l-yIV3-fliiomphenvlV5-tetrazol-l-yl-methyloxazoIidin-2-one and f5gV3-f4-f4-MethvIimidazo]-1 -yIV3-fluorophenyIV5-tetrazol-2-ylmethvIoxazoIidm-2-one Sodium hydride (50% in oil, 108 mg, 2.25 mM) was stirred m JV^-dunethylformamide (3 ml) under nitrogen, and l#-tetrazole (158 mg, 2.25 mM), dissolved m A^-dimethylformamide (4 ml) added. After stirring for 10 minutes, (5i?)-3-(4-memylimidazol-l-yl-3-fiuorophenyl)-5-methanesuIfonyIoxymethyloxazolidin-2-one (553 mg, 1.5 mM) was added, the mixture heated to 80° for 4 hours. The mixture was diluted with aqueous sodium bicarbonate (30 ml), extracted with ethyl acetate (3 x 20 ml), and the extract washed with water (2 x 20 ml), and brine (20 ml). After drying (magnesium sulfate) and evaporation, the residue was purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 20% methanol in dichloromethane. Relevant fractions of the first eluting product were combined to give the less polar tetrazol-2-yl isomer (269 mg). MSiESE): 344(MHVorC15HMFN702 NMR fDMSO-d^ 8: 2.15 (s, 3H); 3.96 (dd, 1H); 4.34 (t, 1H); 5.17 (dd, 1H); 5.27 (dd, 1H); 5.33 (m, 1H); 7.21 (d, 1H); 7.37 (dd, 1H); 7.63 (t, 1H); 7.66 (dd, 1H); 7.87 (d, 1H); 9.04 (s, 1H). The second eluting product was the 1-is'omer (166 mg). MSiESJP): 344 (MET) for C^FNA NMR(DMSQ-d^ 5: 2.16 (s, 3H); 3.97 (dd, 1H); 4.31 (t, 1H); 4.96 (d, 2H); 5.21 (m, 1H); 7.21 (d, 1H); 7.39 (dd, 1H); 7.62 (t, 1H); 7.66 (dd, 1H); 7.87 (dd, 1H); 9.48 (s, 1H). The intermediates for these compounds were prepared as follows: 3-Fluoro-4-(4-methvlimidazol-l-yl)nitroben2ene 4-Memylimidazole (45.1 g, 0.55 M) and 7y;N-du^opropylethylamine (161 g, 1.25 M) were dissolved in acetonitrile (800 ml), and 3,4-difluoronitrobenzene (79.5 g, 0.5 M) added. The mixture was stirred and heated to reflux under nitrogen for 24 hours. Solvent was evaporated, the residue dissolved in ethyl acetate (800 ml), washed with water (400 ml), brine (200 ml), and dried (magnesium sulfate). The residue was dissolved in toluene (250 ml), treated with charcoal, filtered, and diluted with hot cyclohexane (75 ml) to crystallise 3-fhioro-4-(4- memylimidazol"l-yl)nitrobenzene (64.7 g). MS (ESQ: 222 (MET) for C10H8FN3O2 NMRfpMSO-ds) 5: 2.18 (s, 3H); 7.29 (s, 1H); 7.92 (t, 1H); 8.07 (s,lH); 8.18(dd,lH); 8.38 (dd, 1H). 5-Arrmio-2-r4-memvlirnidazol-1-ynfluorobenzene 3-Fluoro^-(4-memylirnidazol-l-yl)nitrobenzene (64.7 g, 0.293 M) was dissolved in a mixture of methanol (200 ml) and tetrahydrofuran (800 ml), cooled to 0° under nitrogen, and treated with ammonium formate (99.3 g, 1.46 M) followed by palladium on charcoal (10%, 2.5 g). The mixture was stirred at ambient temperature for 48 hours, filtered through celite, celite washed with methanol (200 ml), and filtrate evaporated to dryness. The residue was partitioned between ethyl acetate (800 ml) and 10% aqueous sodium bicarbonate (250 ml). The organic layer was separated, washed with brine (250 ml), dried (magnesium sulfate) and evaporated to give title compound (50.6 g). MS (ESP): 192(MH^forC10H10FN3 NMRtoMSO-d^ 5: 2.12 (s, 3H); 5.60 (br s, 2H); 6.42 (dd, 1H); 6.47 (dd, 1H); 6.98 (s, 1H); 7.11 (t,lH); 7.60 (s,lH). 5-Benzyloxycarbonylamino-2-(4-methylirnidazol-l-yl)fluorobenzerie 5-Ammo-2-(4-memylimidazol-l-yl)fluorobenzene (50.6 g, 0.265 M) was dissolved in dry dichloromethane (800 ml) under nitrogen, and cooled to -5°. Pyridine (26.1 g, 0.33 M) was added, followed by benzyl chloroformate (49.9 g, 0.292 M) over 30 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium' bicarbonate (5%, 350 ml) was added, the organic layer separated, and the aqueous layer re-extracted with dichloromethane (2 x 200 ml), and combined organics dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (300 ml) to give title product (80 g). MS (ESP): 326(MH0forClgH]6FN3O2 [sfMR (DMSO-d^ 8: 2.15 (s, 3H); 5.16 (s, 2H); 7.13 (s, 1H); 7.31 (dd, 1H); 7.41 (m, 5H); 7.48 (t, IK); 7.57 (dd, IK); 7.78 (s, 1H); 10.15 (br s, IK). r5JgV3~r3-Fluoro-4-(4-rnethy1imidazol-l-yl)phenv1V5-hvdroxymemy1oxazolidiTi-2~r>Tift 5-Benzyloxycarbonylarnmo-2-(4-memylimidazol-l-yl)fluorobenzene (54 g, 0.166 M) was 5 dissolved in a mixture of dry tetrahydrofuran (600 ml) and 1,3-dimemyl-tetrahydropyrhiudin-2-one (100 ml) under nitrogen, cooled to -70°, and treated with a solution of n-butyllithium (1.6M in wohexane, 114 ml), over 30 minutes. After stirring for 30 minutes at -70°, a solution of (i?)-glycidylbutyrate (26.35 g, 0.183 M) in dry tetrahydrofuran (50 ml) was added over 15 minutes. .Stirring was continued for 16 hours allowing the temperature to rise to ambient. ) The mixture was treated with aqueous sodium bicarbonate (5%, 500 ml) and ethyl acetate (800 ml), and undissolved solid was removed and washed well with diethyl ether to give title product (16.3 g). The aqueous layer was further extracted with ethyl acetate (2 x 750 ml), the combined extracts dried (magnesium sulfate) and evaporated, and the residue triturated with diethyl ether. The resulting solid was recrystallised from ethanol to give more product (10.9 g). MS (ESP): 292(MHVorCMHMFN303 NMR fDMSO-dJ 8: 2.13 (s, 3H); 3.56 (dd, IK); 3.68 (dd, IK); 3.86 (dd, IK); 4.11 (t, 1H); 4.73 (m, IK); 5.21 (br, IK); 7.18 (s, IK); 7.45 (dd, IK); 7.60 (t, IK); 7.73 (dd, IK); 7.83 (s, IK). (5Jn-3-f3-Fluoro-4-(4-methy1imidazol-U^ 2-one (5iZ)-3-(3-Fluoro-4-(4-memylimidazol-1 -yl)phenyl)-5-hydroxymethyloxazohdin-2-one (11.8 g, 40.5 mM) was stirred in a mixture of pyridine (200 ml) and triethylamine (4.86 g, 48.2 mM) under nitrogen in an ice-bath. Methanesulfonyl chloride (5.16 g, 45 mM) was added dropwise, and the mixture stirred for 2 hours, allowing the temperature to rise to ambient. Solvent was evaporated, and the residue stirred vigorously with a mixture of aqueous sodium bicarbonate (5%, 200 ml) and isohexane (200 ml). The precipitate was filtered, washed with water then wohexane, and dried. The residue was recrystallised from hot acetone (200 ml) by dilution with isohexane (300 ml) to give the title product (11.7 g), mp 151-153°. MSXEI): 369 (M) for C]5H16FN305S NMRCPMSQ-dJ 5: 2.16 (s, 3H); 3.27 (s, 3H); 3.88 (dd, IH); 4.24 (t, IH); 4.47 (dd, IH); 4.54 (dd, IH); 5.04 (m, IH); 7.20 (d, IH); 7.45 (dd, IH); 7.63 (t, IH); 7.73 (dd, IH); 7.85 (UH). Example 35: f5i?V3- (5i?)-3-(4-(l-Benzyl-l>2,5,6-tetrahyQ^opyridin-4-yl)-3,5-difluorophenyl)-5-hydroxy-methyloxazolidin-2-one (4.67 g, 11.6 mM), 3#-l,3,4-oxadiazol-2-one (1 g, 11.6 mM, J. Het. Chan., 1995, 32,123), and triphenylphosphine (4.58 g, 17.5 mM) were treated with toluene (50 ml) and evaporated to dryness at 50° to remove water traces. The residue was dissolved in dry tetrahydrofuran (100 ml) by stirring under nitrogen in an ice-bath. Diisopropylazo-dicarboxylate (3.53 g, 17.5 mM) was added dropwise, and the mixture stirred 2 hours, allowing the temperature to rise to ambient. Solvent was evaporated and the residue purified by chromatography on a 90 g silica Biotage column, eluting with a gradient increasing in polarity from 0 to 100% ethyl acetate in dichloromethane. Relevant fractions were combined to give the impure product (6.2 g), contaminated with triphenylphosphine oxide. A portion (2 g) of this material was applied in dichloromethane to a 10 g Isolute strong acid SCX column, and eluted with a gradient increasing in polarity from 0 to 50% methanol in dichloromethane to remove neutral impurities, and finally with a mix' of dichloromethane : methanol: concentrated aqueous ammonia 80:16:4. Solvent was evaporated from appropriate fractions, the residue taken up in 10% aqueous phosphoric acid, and reprecipitated with ammonia to give the title product (275 mg). MS (RSP): 469 (MH4) for C^H^NA NMR (DMSO-d^ 6: 2.29 (br, 2H); 2.62 (t, 2H); 3.03 (m, 2H); 3.57 (s, 2H); 3.86 (dd, IH); 4.01 (dd, IH); 4.11 (dd, IH); 4.18 (t, IH); 5.00 (m, IH); 5.78 (s, IH); 7.27 (d, 2H); 7.33 (m, 5H); 8.45 (s, IH). Example 36: r5ig^-3-r4-ri-BenzyI-1.2.S.6-tetrahydropyridin-4-ylV3.5-difluorophenyIV^-r2-oxo-3H-1.3.4-thiadiazol^3-y1methynoxazoIidin-2-one Essentially the procedure of Example 35 was used, but starting with (5R)-3-(4-(l-benzyl- l,2,5,64etrahydropyridm-4-yl)-3,5-difluoropte mg, 2 mM), and 3#-l,3,4-thiadiazol-2-one (214 mg, 2.2 mM, Helv. Chim. Acta, 1982, 65, 2606), and stirring the reaction for 18 hours. After elution from the SCX column, the gum after evaporation was triturated with diethyl ether to give the desired product (291 mg). MS (ESK): 485 (MH4) for C^H^NAS NMR fDMSO-d^ 8: 2.29 (br, 2H); 2.60 (t, 2H); 3.03 (m, 2H); 3.57 (s, 2H); 3.85 (dd, IH); 4.18 (overlapping m, 2H); 4.29 (dd, IH); 5.03 (m, IH); 5.76 (s, IH); 7.26 (d, 2H); 7.32 (m, 5H); 8.56 (s^ IH). Example 37: r5^-3-f4-f3.6-Dihydro-2g-pvraii-4-vl>-3-fliiorophenyn-5-f3-methvl-2-oxo-2.3-dihydrojmidazoI-l -ylmethyl) oxazoIidin-2-on e A. solution of l-methyhrnidazolidin-2-one (80 mg, 0.82 mM, Heterocycles, 1987,26, 3153) in irmethylsulfoxide (1 ml) was treated with sodium hydride (55% in oil, 40 mg, 0.92 mM) at ambient temperature under nitrogen. After stirring for 20 minutes, (5JR)-3-(4-(3,6-dihydro-ZH-pyran-4-yl)-3-fiuorophenyl)-5-memanesulfonyloxymemyloxazoHdin-2-one(300mg, 3.81 mM; WO 97-09328) in dimethylsulfoxide (1.5 ml) was added and stirring continued for 1.5 hours. The temperature was then progressively raised to 85°, and heated at this :emperature for 24 hours. After cooling and dilution with water (50 ml), the mixture was jxtracted witii ethyl acetate (3 x 30 ml), and combined extracts washed with brine (20 ml). \fter drying (magnesium sulfate) and evaporation, the residue was purified by chromato¬graphy on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in )olarity from 0 to 6% methanol in dichloromethane. Relevant fractions were combined to rive the title product (60 mg). 4S (ESP): 374(MH+)forC19H20FN3O4 NIMR (DMSO-d^ 8: 2.41 (s, 2H); 3.08 (s, 3H); 3.76-3.95 (overlapping m, 5H); 4.15 (t, .H); 4.20 (m, 2H); 4.92 (m, IH); 6.08 (s, IH); 6.50 (m, 2H); 7.25 (d, IH); 7.40 (m, 2H). Example 38: (5J?V3-r4-n.fi-L^hydro-2Jy-pvran-4-yn-3-fluorophenvn-5-f3-metTiyl-2-thiQrQ-2.3-dihydroimidazol-l-ylmethynorazoIidin-2-one Essentially the procedure of Example 37 was used, but starting with (5i?)-3-(4-(3,6-dihydro-2ZT-pyran-4-yl)-3-fluorophenyl)-5-methanesdfonyloxvme1nyloxazoHdin-2-one(300mg, 0.81 mM), and l-methyltmidazolidin-2-thione (100 mg, 0.88 mM) and heating the reaction at 60° for 1.5 hours. Chromatography on two columns gave the desired product (29 mg). MS (RSP): 390(Mir)forCli>H20FN3O3S NMR (DMSO-d^ 8: 2.42 (br s, 2H); 3.46 (s, 3H); 3.80 (t, 2H); 4.02 (dd, IK); 4.20 [overlapping m,3H); 4.27-4.47 (m, 2H); 5.09 (m,lH); 6.09 (br s, 1H); 7.17 (m,2H); 7.29 [dd, 1H); 7.38 (d, IK); 7.45 (dd, 1H). Example 39: r5i?V3-r4-Methv1thiophenvn-5-a.2.3-triazol-l-vlTnethvnoxazolidin-2-one (JJ?)-3-(4-Methyltbiophenyl)-5-a2idomemyloxazohdin-2-one (1.62 g, 6.14 mM) was iissolved in dioxane (30 ml), treated with norbomadiene (2.98 g, 31.5 mM) and heated under eflux for 6 hours. After removal of the solvent, the residue was dissolved in the minimum of lot ethyl acetate, filtered, cooled, then diluted with isohexane to precipitate the desired >roduct (600 mg). dS (CI): 291 (MIT) for C13H14N402S 4MR (270 MHz. CDCU 5: 2.46 (s, 3H); 3.92 (dd, 1H); 4.15 (t, 1H); 4.79 (m,2H); 5.04 m, IK); 7.23 (d, 2H); 7.31 (d, 2H); 7.74 (d, IK); 7.80 (d, 1H). "he starting material is described by WA Gregory et al, J.Med.Chem., 1989,32,1673. :xample40: (5gV3-f4-MethvlsulfnnvlphenvIV5-(1.2.3-triazol-l-yImethynoxazolidin-2-ne ;5Ji)-3-(4-MemyltMophenyl)-5 iM) was dissolved in dichloromethane (15 ml), treated with 3-chloroperoxy-benzoic acid 50%, 1.24 g, 3.59 mM), and stirred at ambient temperature for 3 hours. After removal of the Dlvent, the residue was triturated with diethyl ether and filtered, to give the desired product 550 mg). fS(CT>: 323 (MIT) for C13HI4N404S MR (270 MHz. CDC^ + DMSO-d^) 5: 2.57 (s, 3H); 3.52 (dd, 1H); 3.78 (t, IK); 4.36 (m, 2H); 4.67 (m, IH); 7.18 (d, 2H); 7.26 (d, IH); 7.38 (d, 2H); 7.47 (d, IH). Example 41: r5i?)-3-(4-f-BiitvIpheriyn-5-rt.2.3-triazol-1 -vlmethynoxazolidin-2-one (5i?)-3-(4-f-Butylphenyl)-5-azidomethyloxazolidin-2-one (400 mg, 1.46 mM) was dissolved i in dioxane (8 ml), treated with norbomadiene (1.3 g, 14.1 mM) and heated under reflux for 6 hours. After removal of the solvent, the residue was dissolved ethyl acetate, and purified by flash chromatography on silica, eluting with the same solvent. Relevant fractions were combined to give the desired product (260 mg, mp 140-142°). MS (ED: 300 (M^) for ClfrH20N4O2 NMR (270 MHz. CDC^ 5: 1.26 (s,9H); 3.90 (dd, IH); 4.15 (t, IH); 4.77 (m,2H); 5.03 (m, IH); 7.30 (d, 2H); 7.36 (d, 2H); 7.72 (d, IH); 7.79 (d, IH). (5i^)-3-(4-^Butylphenyl)-5-a2idomethyloxazohdin-2-one may be prepared by the routes described in WA Gregory et al, J.Med.Chem., 1990, 33,2569. Example 42: (55)-3-f4-MethvlsuIfonyIphenylV5-(imidazoI-l-ylmethyl)oxazolidin-2-one (5iS)-3-(4-Methylthiophenyl)-5 The intermediate for this compound was prepared as follows: (5^-3-r4-Methvlthiopheriy1)-5^irnidazol-t-v1rnethvlloxazolidin--2-one Sodium hydride (80% in oil, 23 mg, 0.77 mM) was stirred under nitrogen in iV^-dimethylformamide (5 ml), imidazole (52 mg, 0.77 mM) added, and stirring continued for 10 minutes. (5J?)-3-(4-Methyl1mophenyl)-5-memanesulfonyloxymethyloxazolidm-2-one (200 mg, 0.63 mM) was dissolved in JV^dimethylformamide (5 ml), added to the above, and the mixture stirred 18 hours at ambient temperature. After diluting with water (30 ml), the mixture was extracted with ethyl acetate (30 ml), the extract washed with brine (25 ml), dried (magnesium sulfate) and evaporated. The residue was triturated with diethyl ether, and filtered to give the desired product (129 mg, mp 129-131 °). MS (CI): 290(MHr)forC14H15N3O2S NTvnm70MHz.CDC13;> S: 2.48 (s, 3H); 3.66(dd,lH); 4.11 (t, 1H); 4.28 (dd, 1H); 4.37 (dd, 1H); 4.91 (m, 1H); 7.11 (brs,2H); 7.25 (d,2H); 7.35 (d,2H); 7.58 (brs, IE). (5i?)-3-(4-Methylthiophenyl)-5-memaaesulfonyloxymethyloxazoHdin-2~one may be prepared from the corresponding 5-hydroxymethyl compound (described by WA Gregory et al, J.Med.Chem., 1989, 32,1673) by a route analogous to that used for the methanesulfonyl intermediate of Example 1. Example 43: (5^)-3-(4-MethvIthiophenvn-5-fpvra7:n^l-vlmethvnoxazolidiii-2-one Sodium hydride (80% in oil, 63 mg, 2.1 mM) was stirred under nitrogen in A^-dimethylformamide (2 ml), (Ji?)-3-(4-methylthiophenyl)-5-methanesulfonyloxymethyl- oxazolidin-2-one (630 mg, 2 mM) dissolved in A^dimethylformamide (10 ml) added, followed by pyrazole (140 mg, 2 mM) dissolved in iV^-dimethylformamide (2 ml). Stirring was continued for 1.5 hours at ambient temperature. After diluting with water (30 ml) and stirring for 1 hour, the precipitate was filtered to give the desired product (190 mg, mp 72-73°). VISfEn: 289 (W) for C14H15N302S WTO (9.70 MHz. fDCI^ 8: 2.47 (s, 3H); 3.96-4.10 (m,2H); 4.50 (d,2H); 4.99 (m, 1H); >.29 (m, 1H); 7.26 (d, 2H); 7.36 (d, 2H); 7.53 (m, 2H). Sample 44: r5J?V3-f3.5-Difluoro-4-f3.6-dihvdrn-171 -dioxn-2y7'-thiopvTan-4-ynphenvn- UT.2.3-triazol-l-vlmethvnoxazo]idiD-2-nnft3Tid(^gUW3.5-Difluoro-4-0.6-dihvdro-l.l- linvn-2?T-thiopyran-4-vnphenyIV5-fl.2.3-tria7nl-2-ylmethvnnxazolidin^2-oiie iodium hydride (50% in oil, 72 mg, 1.5 mM) was stirred under nitrogen in N-Ndrmethylformarnide (3 ml), and a solution of 1,2,3-triazole (104 mg, 1.5 mM) in N,Af-dimemylformamide (4 ml) added, and stirring continued for 10 minutes. (5i?)-3-(3,5-Difluoro-4-(2,6-dihydro-1,1 -dioxo-2^r-thiopyran-4-yl)phenyl)-5-methanesulfonyl-oxymethyloxazolidin-2-one (437 mg, 1 mM) was added as solid, and the reaction heated at 75° for 1.5 hours. The mixture was diluted with aqueous 5% sodium bicarbonate (25 ml), extracted into ethyl acetate (2 x 20 ml), washed with water and brine (20 ml of each), dried (magnesium sulfate) and evaporated. The residue was purified by chromatography on a 10 g i silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 100% ethyl acetate in dichloromethane. Relevant fractions were combined to give the 2-triazole as the less polar product (250 mg) and the 1-triazole as the more polar product (100 mg). 2-Triazole: MS (ESP): 411 (MB) for C17H16F2N404S NMR (DMSO-d^ 6: 2.82 (m,2H); 3.32 (m overlapped by H20,~2H); 3.90 (dd overlapped by m, 3H); 4.23 (t, 1H); 4.86 (m, 2H); 5.22 (m, 1H); 5.74 (t, 1H); 7.28 (d, 2H); 7.83 (s, 23). l-Triazole: MS (ESP): 411 (MH4) for C17H16F2N404S NMR (pMSO-dfll 5: 2.82 (m, 2H); 3.32 (m overlapped by H20, ~2H); 3.90 (dd overlapped bym, 3H); 4.21 (t, 1H); 4.82 (m, 2H); 5.16 (m, 1H); 5.75 (t, 1H); 7.30 (d, 2H); 7.87 (d, 1H); 8.18 (d,lH). The intermediates for this compound were prepared as follows: 4-(4-Ammo-2.6-difluorQ-phenylVtetrahydro-thiopyran-4-ol 3,5-Difluoroaniline (12.9 g, 0.1 M) in dry tetrahydrofuran (400 ml) was stirred and cooled under nitrogen to -78°. w-Butyllithium (1.6M in hexanes, 131 ml, 0.21 M) was run in slowly over 15 minutes, mamtaining the temperature below -65°. Stirring was continued at the same temperature for 30 minutes, then trimethylsilyl chloride (22.8 g, 0.21 M) in tetrahydrofuran (100 ml) was added dropwise over 15 minutes. The temperature was then allowed to rise to ambient, and the mixture stirred overnight After recooling to -78°, further rc-butylKthium (1.6M in hexanes, 68.8 ml, 0.11 M) was added dropwise below -70°, and stirring continued for 5 hours to form anion. A solution of tetrahydrothiopyran-4-one (12.5 g, 0.107 M) in tetrahydrofuran (80 ml) was added dropwise, keeping the temperature below -70°, and the temperature allowed to warm to ambient overnight. The mixture was cooled in an ice-bath and acidified to pH NMR (CDCl^ 5: 2.27 (d,2H); 2.40 (t,4H); 2.65 (t, 1H); 3.27 (t,2H); 3.82(brs,2H); 6.17 (d, 2H). 4- 4-(4-Ammo-2,6-d^fluoro-phenyl)-tetrahydro-tMopyran-4-61 (16.7 g, 68 mM) was suspended in a mixture of concentrated hydrochloric acid (200 ml), water (50 ml) and acetic acid (200 ml), BHT (50 mg) added, and the whole stirred under nitrogen at 80° for 18 hours. After cooling, the mixture was made basic by cautious addition of concentrated ammonia, and ice-water. The mixture was then extracted with diethyl ether (2 x 300 ml), the extracts washed with water (100 ml), brine (200 ml) and dried (magnesium sulfate). Evaporation gave the desired product as a cream solid (15.2 g). MS fESP;>: 244 (MlT) for CnHuF2NS NMR (CDCl^ 5: 2.48 (m,2H); 2.82 (t,2H); 3.30 (m,2H); 3.80 (br s, 2H); 5.87 (s, 1H); 6.17 (d, 2H). 4-r4-Benzyloxycarbony1flrnirio-?..6-difluorophenvD-5.6-dihydro-2g-thiopvran 4-(4-Aiiu^o-2,6-difluorophenyl)-5,6-dihydro-2fl"-thiopyran (15.0 g, 66 mM) was dissolved in dry dichloromethane (250 ml), pyridine (9.45 g, 113 mM) added, and the whole stirred under nitrogen at -20°. Benzyl chloroformate (17.1 g, 100 mM) in dry dichloromethane (25 ml) was added dropwise, and the mixture allowed to warm to ambient over 18 hours. The mixture was washed with hydrochloric acid (1M, 2 x 200 ml), then brine (200 ml) and dried (magnesium sulfate). Evaporation to a small volume and dilution with isohexane gave the desired product as a white solid (22.5 g). MS (ESP): 362 (MH+) for C19H17F2N02S NMR (DMSO-dfi) 5: 2.38 (m, 2H); 2.78 (t, 2H); 3.24 (m, 2H); 5.15 (s, 2H); 5.89 (s, 1H); 7.17 (d, 2H); 7.38 (m, 5H); 10.18 (s, 1H). f5J?V3^3.5»Difluoro^-(2.6-dihvdro-2^-thiopwan-4-vDphenvlV5-hvdroxvmethvloxazo1idin-2-one 4-(4-Benzyloxycarbonylamino-2,6-difluorophenyl)-5,6-dihydro-2iy-thiopyran (22 g, 61 mM) was dissolved in dry tetrahydrofuran (235 ml), stirred under nitrogen, and cooled to -78°. n-Butyllitibium (1.6M in hexanes, 38.2 ml, 0.61 mM) was run in slowly over 20 minutes, mamtaining the temperature below -65°. Stirring was continued at the same temperature for 10 minutes, then (R)-glycidyl butyrate (8.8 g, 61 mM) in tetrahydrofuran (15 ml) was added dropwise over 10 minutes, maintaining the temperature below -60°. The temperature was then allowed to rise to ambient, and the mixture stirred overnight. Methanol (25 ml) was added, and stirring continued for 10 minute, before the addition of aqueous sodium bicarbonate (5%, 200 ml) and extraction with ethyl acetate (400 ml). After washing with sodium bicarbonate (5%, 100 ml), then brine (100 ml) and drying (magnesium sulfate), the solution was evaporated, the residue redissolved in dichloromethane, and product precipitated with isohexane. Recrystallisation from isopropanol gave the desired product (16.2 g). MS fESPV- 328 (MIT) for C35HI5F2N03S NMR fDMSO-d^ 8: 2.39 (m,2H); 2.80 (t,2H); 3.27 (m,2H); 3.53 (m, 1H); 3.66 (m, 1H); 3.81 (dd, 1H); 4.07 (t, 1H); 4.69 (m, 1H); 5.21 (t, 1H); 5.93 (s, 1H); 7.33 (d, 2H). r5i?V3-r3.5-Difluoro-4-(2.6-dihydro-l.l-dinxo-2^thinpvran-4-yl)phenyl)-5-hvdroxvmethyl- oxazolidin-2-one (JJ?)-3 2-one (6.54 g, 20 mM) was dissolved in dichloromethane (250 ml), and stirred at ambient temperature. 3-ChJoroperoxy-benzoic acid (80%, 10 g, 46 mM) dissolved in dichloromethane (90 ml) was added dropwise, and stirring continued for 1 hour. Excess aqueous sodium metabisulfite was added, and stirring continued for 10 minutes. Excess dichloromethane (~1.5- L) was added to dissolve all organics, and the organic phase separated. After washing ' with aqueous sodium bicarbonate (200 ml) and drying (magnesium sulfate), the filtrate was evaporated to a small volume, and the desired product filtered (6.5 g). MS (ESP): 360 (MH+) for C15H15F2N05S NMRrDMSO-d£) 5: 2.82 (m, 2H); 3.34 (m overlapped by H20,2H); 3.52 (m, IH); 3.67 (m, IH); 3.83 (dd, IH); 3.91 (m, 2H); 4.08 (t, IH); 4.82 (m, IH); 5.22 (t, IH); 5.83 (t, IH); 7.38 (d, 2H). (5igV3-r3.5-Difluoro-4-(2.6-dihvdrn-lJ-dioyn-2^-thiopvran^vnphenyn-5-methane~ sulfonyloxymethyloxazolidin-2-one (5i0-3-(3,5-Difluoro~4-(2,6-dmydro-1,1-dioxo-2^ oxazolidin-2-one (6.1 g, 17 mM) was dissolved in dry tetrahydrofuran (400 ml), and stirred under nitrogen in an ice-bath. Triethylamine (2.4 g, 23.7 mM) was added, followed by dropwise addition of methanesulfonyl chloride (2.33 g, 20.3 mM). After stirring for 2 hours at 0°, the mixture was diluted with aqueous sodium bicarbonate (400 ml) and tetrahydrofuran evaporated from the mixture. The residue was extracted with dichloromethane (2 x 500 ml), the extract dried (magnesium sulfate). After evaporation of the filtrate to a small volume, it was diluted with isohoxane to precipitate the desired product filtered (8.0 g). MS_(ES£): 438 (MH) for C16H17F2N07S2 NMR (DMSO-d^ 8: 2.82 (m,2H); 3.25 (s, 3H); 3.33 (m overlapped by H20,~2H); 3.84 (dd, IH); 3.93 (m, 2H); 4.19 (t, IH); 4.48 (m, 2H); 5.03 (m, IH); 5.85 (s, IH); 7.38 (d, 2H). Example 45: r5i?V3-f;4^ri-Ben2vI-1.2.5.6-tetrahydropvridm-4-vIV3-fluorophepyIV5-(1.2.3"triazoI-l-yImethynoxazolidin-2-one (5i?)-3-(4-(l-Ben2yl-l,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-azidomethyl-oxazolidin-2-one (4.55 g, 11.2 mM) and norbomadiene (5.15 g, 56 mM) were dissolved in dioxan (50 ml) and heated under reflux for 4 hours. The reaction mixture was evaporated and the product isolated by MPLC on silica, eluting with 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product as a gum which crystallised on trituration with diethyl ether (2.9 g). MS (ESP): 434 (MH4) for C24H24FN502 NMRrDMSO-dg) 5: 2.43 (s, 2H); 2.63 (t, 2H); 3.04 (d, 2H); 3.69 (s, 2H); 3.89 (dd, 1H); 4.24 (t,lH); 4.84 (d,2H); 5.14 (m,lH); 5.98 (s, 1H); 7.32 (m, 8H); 7.75 (s, 1H); 8.15 (s, 1H). The intermediates for this compound were prepared as follows: r57?)-3-r4-(l-Benzyl-1.2.5.6-tetrahvdropvridin-4-yl)-3-fluorophenyD-5-methanesulfonvl- oxymethvloxazolidin-2-one (5ii)-3-(4-(l-Benzyl-l,2,5,6-tetrahydropyridm^^ oxazolidin-2-one (4.97 g, 13 mM; WO 97-30995) was reacted by essentially the technique of the related intermediate of Example 1, to give the desired product without chromatography after trituration with diethyl ether (5.78 g). MS (ESP): 461 (MH) for C^FNAS NMRfDMSO-d^ 5: 2.43 (s,2H); 2.62 (t,2H); 3.03 (d,2H); 3.25 (s, 3H); 3.58 (s,2H); 3.84 (dd, 1H); 4.18 (t, 1H); 4.47 (m, 2H); 5.02 (m, 1H); 5.98 (s, 1EQ; 7.32 (m, EH). r5J?)-3-r4-ri-Ben2rvl-lr2.5.6-tetrahydropvridin-4-yIV3-fluorophenyl)-5-azidomethyl- oxazolidin-2-one (5i?)-3-(4-(l-Benzyl-l,2,5,6-tetrahydropyridm-4-yl)-3-fluorophenyl)-5-memanesm,fonyl- oxymethyloxazolidin-2-one (5.61 g, 12.2 mM) was reacted by essentially the technique of the related intermediate of Example 1, except that dimethylsulfoxide was used as solvent, to give the desired product (4.66 g). MS (ESP): 408 (MET) for C2ZH22FN502 NMRfDMSO-d^ 8: 2.45 (s, 2H); 2.62 (t, 2H); 3.05 (d, 2H); 3.56 (s, 2H); 3.71 (m, 3H); 4.15 (t, 1H); 4.88 (m, 1H); 5.95 (s, 1H); 7.31 (m, 8H). Example 46: f5gV3-(4-fl .2.5.6-tetrahvdropvridiii-4-yn-3-fliiorophen vlVS-fl ,2.3-triazol-l-vlmethynoxazoIidin-2-nne (5iO-3 ylmethyl)oxazolidin-2-one (2.75 g, 6.35 mM) and A^/^-diisopropylethylamine (165 mg, 1.27 mM) in dichloromethane (30 ml) at 0-4° under nitrogen were treated dropwise with 1-chloroethyl chloroformate (1.09 g, 7.62 mM). The solution was stirred for 30 minutes, then evaporated. The residue was purified by MPLC on silica, eluting with a gradient from 0-20% acetonitrile in ethyl acetate, to give the intermediate carbamate as a crystalline solid. This was heated under reflux in methanol (50 ml) for 20 minutes. Evaporation of the solvent and trituration with ethyl acetate gave the desired product as its hydrochloride salt (1.94 g). MS (ESP): 344(MEr)forC17H18FN502 NMRfDMSO-dfi) 8: 2.63 (s, 2H); 3.24 (2d, 2H); 3.72 (d, 2H); 3.92 (m, IH); 4.23 (t, IH); 4.83 (d, 2H); 5.15 (rn, IH); 6.03 (s, IH); 7.29 (dd, IH); 7.42 (m, 2H); 7.76 (s, IH); 8.17 (s, IH); 9.24 (s,2H); +1H for HC1 salt. Example 47: (5K)-%44-fl -Formvl-1.2.5.6-tetrahvdropyridin-4-vlV3-fliiorophenyn-5-r1.2.3-triazol-l-ylmethyI)oxazolidin-2-one ;5i?)-3-(4-(l,2,5,6-Tetrahydropyria^4-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-ylme 3xazolidin-2-one hydrochloride (450 mg, 1.19 mM) and triemylarnine (156 mg, 1.56 mM) vere heated under reflux for 48 hours in ethyl formate (20 ml). The reaction mixture was liluted with ethyl acetate (30 ml) and washed with water and brine. Drying (sodium sulfate) ind evaporation gave a gum which crystallised on trituration with diethyl ether to give the lesired product (358 mg). vlS (ESP): 372(MH+)forClgHJ8FN503 ■JMR (DMSO-d^ 5: 2.38 (br, 2H); 3.59 (m, 2H); 3.91 (dd, IH); 4.06 (dd, 2H); 4.22 (t, H); 4.83 (d, 2H); 5.13 (m, IH); 6.00 (2 x s, IH); 7.23 (dd, IH); 7.38 (m, 2H); 7.75 (s, H); 8.14 (2 xs, IH); 8.17 (s, IH). Example 48: f5/gV3-r4-(l-Benzyl-1.2.5.6-tetrahydropyridm-4-vn-3.5-difluoropheiivn-S-fl.2.3-triazo]-l-v]methvno\azolidm-2-one (5i?)-3-(4-(l-Berizyl-l,2,5J64etrahydropyridm-4-yl)-3,5-oMuorophenyl)-5-azidometb.yl- oxazolidin-2-one (850 mg, 2 mM) was reacted by essentially the teclmique of Example 45, to give the desired product (550 mg). MS (ESP): 452 (MET) for C24H23F2N502 NMRfDMSO-d^ 5: 2.29 (s, 2H); 2.61 (t, 2H); 3.05 (s, 2H); 3.59 (s, 2H); 3.88 (dd, IH); 4.21 (t, IH); 4.80 (d, 2H); 5.15 (m, IH); 5.78 (s, IH); 7.29 (m, 7H); 7.75 (s, IH); 8.15 (s, IH). The intermediates for this compound were prepared as follows: f5JgV3-f4-n-Beri7^1-1.2.5.6-tetrahydropyridm^ oxymethyloxazolidm-2-one (5i?)-3-(4"(l-Benzyl-l,2s5J64etrahydropyriaUn-4-yl)-3,5-diiluorophenyl)-5-hydroxymemy^ oxazolidin-2-one (WO 99-64417; 8.4 g, 21 mM) was reacted by essentially the technique of the related intermediate of Example 1, to give the desired product without chromatography after trituration with diethyl ether (9.38 g). NMR(DMSO-d^ 8: 2.30 (s, 2H); 2.62 (t, 2H); 3.05 (d, 2H); 3.24 (s, 3H); 3.58 (s, 2H); 3.82 (dd, IH); 4.17 (t, IH); 4.46 (m, 2H); 5.02 (br s, IH); 5.78 (s, IH); 7.30 (m, 7H). (5J?)-3-r4-(l-Ben2yl-1.2.5.6-tetrabvdrop\nidin-4-ylV3.5-difiuoropheny1)-5-azidomethvl- nxazolidm-2-one (5it)-3-(4-(l-Beoi2yl-l,2J5,6-te1xahydropyridm-4-yl)-3,5-drfluorophenyl)-5-methanesulfonyl- Dxymethyloxazolidin-2-one (4.06 g, 8.5 mM) was reacted by essentially the technique of the related intermediate of Example 1, except that dimethylsulfoxide was used as solvent. After work-up, the residue was purified by MPLC on silica, eluting with 50% z'sohexane in ethyl icetate, to give the desired product as a gum which crystallised on trituration with ethyl icetate and wohexane (2.84 g). VTS flBSP): 408 (MH+) for CaE3aiF2NJ02 sJMR rPMSO-df) 6: 2.31 (s,2H); 2.62 (t,2H); 3.05 (d,2H); 3.60 (s,2H); 3.75 (m, 3H); 4.12 (t, IH); 4.90 (m, IH); 5.88 (s, IH); 7.30 (m, 7H). Example 49: r5JZV3-f4-(1.2.5.6-tetrahvdropyridm-4-vIV3.5-difluorophenvlV5-a.2.3-triazol-l-ylmethyDoxazoIidin-2-nne (5i?)-3-(4 ylmethyl)oxazoridin-2-one (1.13 g, 2.5 mM) was reacted by essentially the technique of Example 46, to give the desired product as its hydrochloride salt (665 mg). MS (ESP): 362 (MET) for C17H17F2N502 NMR fDMSO-d;> 8: 2.55 (overlapping DMSO, ~2H); 3.29 (overlapping H20, ~2H); 3.79 (d52H); 3.90(dd,lH); 4.23 (t, IH); 4.82 (d,2H); 5.19 (m, IH); 5.90 (s, IH); 7.31 (d,2H); 7.76 (s,lH); 8.18 (s, IH); 9.25 (s,2H); +1H for HC1 salt Example 50: r5/?V3-(4-a-Formvl-1.2.5.6-tetrahydropyridin-4-vn-3.5-difluorophenvn-5-(lf2f3-triazol--l-y]methyI)oxazolidin-2-one (5J?)-3-(4-(l,2,5,6-Tetrahydropyridm^-yl)-355-difiuorophenyl)-5-(l,2,3-tria2ol4 oxazolidin-2-one hydrochloride (450 mg, 1.13 mM) was reacted by essentially the technique of Example 47, to give the desired product (387 mg). MS (ESP): 390 (MPT) for C18H17F2N503 NMRrDMSO-d^ 5: 2.33 (2 x s, 2H); 3.60 (m,2H); 3.90 (dd, IH); 4.05 (2 x d, 2H); 4.23 (t, IH); 4.82 (d, 2H); 5.18 (m, IH); 5.90 (2 x s, IH); 7.28 (d, 2H); 7.75 (s, IH); 8.13 (2 x s, IH); 8.16(2xs,lH). Example 51: r5flV3-(4-(;i>(2-AcetoxyacetyIV1.2.5.6-tetrahydropvridin-4-yn-3.5-difluoro-phenyl)-5-(1.2.3-triazol-l-ylmethyI)oxazolidin-2-one A solution of (5i?)-3-(4-(l,2,5,6-tetrahydropyridin-4-yl)-3,5-difluorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazolidin-2-one hydrochloride (650 mg, 1.64 mM) in acetone (20 ml) and water (10 ml), was treated with sodium bicarbonate (1.38 g, 16.4 mM) and the mixture cooled to 0-4°. Acetoxyacetyl chloride (448 mg, 3.28 mM) was added dropwise and the reaction mixture stirred at 0-4° for 20 minutes before allowing to warm to ambient temperature. After dilution with water the mixture was extracted well with ethyl acetate. The organic phase was separated, dried (sodium sulfate), solvent evaporated, and the residue triturated with diethyl ether to give the desired product (702 mg). MSiESE}: 462 (MET) for G21H2IF2N505 NMR (DMSO-d^ 8: 2.09 (s, 3H); 2.36 (2 x s, 2H); 3.60 (m,2H); 3.89 (dd, IH); 4.09 (br, 2H); 4.23 (t, IH); 4.83 (m, 4H); 5.18 (m, IH); 5.89 (s, IH); 7.29 (d, 2H); 7.78 (s, IH); 8.20 (s} IH). Example 52: fr5/?V3-r4-(l-r2~Hvdro]cyacetyn-1.2.5.6-tetrahydropvridin-4-vn-3.5-diflnorophenyI)-5-(1.2T3-triazol-l-ylmethyI)oxazoIidin-2-one (5i?)-3 NMRfDMSO-d^ 5: 2.32 (2 x s, 2H); 3.54 (br, IH); 3.68 (br, IH); 3.99 (dd, IH); 4.10 (m, 4H); 4.24 (t, IH); 4.58 (m, IH); 4.82 (d, 2H); 5.18 (m, IH); 5.88 (br, IH); 7.28 (d, 2H); 7.77 (sslH); 8.17 (s, IH). BTrample 53: (5flV3-f4-f Wf4SV2.2-dimethvl-l .3-dioxoIane-4-carbonvIVI .2.^.6-tetrahydropyridin-4-yl)"3.5-dijHuorophenyI)-5-(lr2.3-triazol-l-ylmethyI)oxazoIidin-2-one A. solution of (Ji?)-3-(4-(l,2,5,6.terrahydropyridm^-yl)-3,5-difluorophenyl)-5-(l,2,3-triazol-L-yhnethyl)oxazolidin-2-one hydrochloride (650 mg, 1.64 mM) in dry dichloromethane (20 nl) at 0-4°, was treated with pyridine (648 mg, 8.2 mM) followed by dropwise addition of y1S)-2,2-dimethyl-l,3-dioxolane-4-carbonyl chloride (430 mg, 2.64 mM). The solution was allowed to warm to ambient temperature and stir for 1 hour. The reaction mixture was washed with water and brine, dried (sodium sulfate) and evaporated to a gum which crystallised readily on trituration with diethyl ether to give the title compound (788 mg). MS (ESP): 490 (ME") for C^H^NA NMR 8: 1.32 (d, 6H); 2.34 (2x s, 2H); 3.87 (dd, IH); 4.09 (t, IH); 4.20 (t, 2H); 3.00-4.30 (m, 4H); 4.80 (d, 2H); 4.90 (m, IH); 5.15 (m, IH); 5.89 (s, IH); 7.25 (d, 2H); 7.75 (s, IH); 8.17 (s, IH). Example 54: f5Jr>-344-fWf2^-2.3-Dihvdroxvpropionvr>-1.2.5.6-tetrahvdropvHdin-4-ylV3.5-difloorophenvIVS-ri.2.3-triazoI-l-vImetliynoxazolidin-2-one To a stirred solution of (5i2)-3-(4-(l-((4S)-2,2-dime^ tetrahydropyridm-4-yl)-3,5-difluorophen mg, 1.43 mM) in tetrahydrofuran (25 ml) was added aqueous hydrochloric acid (1M, 15 ml) and the mixture stirred at ambient temperature for 2 days. Solvent was evaporated and the residue treated with water (10 ml). Aqueous sodium acetate (10%, 10 ml) was added, and the precipitate filtered and washed with ethanol and diethyl ether to give the title compound (514 mg). MS (ESP): 450 (MET) for C20H21F2N5O5 NMRfDMSO-dg) 6: 2.33 (m, 2H); 3.51 (m, 3H); 3.71 (br, 2H); 3.90 (dd, 1H); 4.00-4.40 (complex, 3H); 4.67 (m, 1H); 4.82 (d,2H); 4.92 (m,lH); 5.15 (m,lH); 5.87 (s,lH); 7.27 (d, 2EQ; 7.76 (s, 1H); 8.17 (s, 1H). Example 55: (5ff>3-(4-fl -^-AcetoxyacetylVI .2.5.6-tetrahydropyridin-4-ylV3-fIuoro-phenyfl-5-fl .2.3-triazol-l -ylmeth vftoxazoIidm-2-one (Jie)-3-(4 oxazolidin-2-one hydrochloride (803 mg, 2.11 mM) was reacted by essentially the technique of Example 51, to give the desired product (767 mg). MS (ESP): 444 (MH) for CI1H22FN5Os NMR (DMSO-dg) 8: 2.00 (s, 3H); 2.41 (s, 2H);. 3.59 (m, 2H); 3.90 (dd, 1H); 409 (s, 2H); 4.25 (t, 1H); 4.83 (m, 4H); 5.15 (m, 1H); 5.98 (s, 1H); 7.25 (dd, 1H); 7.40 (m, 2H); 7.76 (s, 1H); 8.17 (s, 1H). Example 56: f5J?V3-f4-n-(2-HydroxyacetvlV1.2.5.6-tetrahydropvridin-4-yi;>-3-flnoro-phenvn-5-a.2.3-triazoI-l-yImethynoxazolidin-2-one (5if)-3-(4 triazoM-ylmethyl)oxazolidin-2-one (443 mg, J mM) was reacted by essentially the technique of Example 51, to give the desired product (370 mg). MS (ESP): 402(MH4)forC19H20FNsO4 KMR (DMSO-d;> 5: 2.45 (s, 2H); 3.60 (m, 2H); 3.89 (dd, 1H); 4.12 (m, 4H); 4.25 (t, 1H); 4.55 (m, 1H); 4.82 (d, 2H); 5.15 (m, 1H); 6.00 (d, 1H); 7.25 (dd, 1H); 7.40 (m, 2H); 7.75 (s, 1H); 8.16 (s, 1H). Example 57: (5K)-3-(4-(l-((4S)-2.2-dimethy\A .3-dioxo]ane-4-cai'bonylVl,2.5.6-tetrahvdropyridm-4-ylV3-flnorophenyIV5-n.2.3-triazol-l-vImethvDoxazolidin-2"Qne (5J0-M4-(l,2,5,6-Tetrahydropyridm-4-yl)-3-fl^^ oxazolidin-2-one hydrochloride (651 mg, 1.71 mM) was reacted by essentially the technique of Example 53, to give the desired product (697 mg). MS fESPV 472 (MIT) for C^H^FNA NMR toMSO-d^ 8: 1.31 (m, 6H); 2.40 (s, 2H); 3.60-4.30 (complex, 8H); 4.83 (d, 2H); 4.90 (m, 1H); 5.15 (m, 1H); 6.00 (s, 1H); 7.15 (dd, 1H); 7.40 (m, 2H); 7.73 (s, 1H); 8.15 (s, 1H). Example 58: r5i?V3--r4-fl-ra (5£)-3 fluorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazoHdm-2-one (600 mg, 1.27 mM) was reacted by essentially the technique of Example 54, to give the desired product (443 mg). MS fESPI: 432 (MH) for C^FNA NMR.rDMSO-d,') 8: 2.40(br,2H); 3.35-3.85 (complex, 4H); 3.90(dd,lH); 4.10 (s,lH); 4.25 (t, 2H); 4.35 (m, 1H); 4.65 (m, 1H); 4.82 (d, 2H); 4.93 (m, 1H); 5.13 (m, 1H); 6.00 (s, 1H); 7.22 (dd, 1H); 7.38 (m, 2H); 7.73 (s, 1H); 8.15 (s, 1H) Example 59: r5JgV3-r4-ri-BRTizvI-1.2^.fi-tetrahvdropvridin-4-yIV3.5-difliinrophenvn-5-fl^.g-triazoI^-vimethvDoxazoIidin^-one (5i?)-3-(4-(l-B erizyl-1,2,5,6-tetrahydrop v^^ oxymethyloxazolidm-2-one (2.39 g, 5.0 mM) was dissolved in A^dimemylfonnamide (25 ml), and treated with 1,2,3-triazole (690 mg, 10 mM) and anhydrous potassium carbonate (1.3 8 g, 10 mM), then stirred at 80° for 3 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, brine, dried (magnesium sulfate) and evaporated to a gum, which was purified by MPLC on silica, eluting with a gradient from 10 to 100% ethyl acetate in isohexane. Combination, of appropriate fractions gave two products as gums which crystallised on trituration with, diethyl ether. The less polar product was identified as the desired product (1.45 g). MS (ESP): 452 (MH+) for C^H^NA NMRtoMSO-d£) 5: 2.31(s,2H); 2.62 (t,2H); 3.05 (d,2H); 3.59 (s,2H); 3.89(dd,lH); 4.21 (t, IH); 4.83 (m, 2H); 5.21 (m, IH); 5.78 (s, IH); 7.27 (m, 7H); 7.82 (s, 2H). The more polar product (760 mg) was identified as the 1-substituted triazole isomer of Example 48. Example 60: (SffWU4-(1 -Benzvl-1.2.5.6-tetrahydropvridm-4-yn-3.5-difluorophenvIV5-Q.2.4-triazoI-l-ylmethynnxaznlidm-2-one (5i?)-3-(4-(l-Benzyl-l,2,5s6-tetrahyd^opvridm-4-yl)-3,5-difluorophenyl)-5-memanesu^ oxymethyloxazolidin-2-one (956 mg, 2.0 mM) was dissolved in TV^V-dimethylformamide (12 ml), treated with 1,2,4-triazole (173 mg, 2.5 mM) and anhydrous potassium carbonate (690 mg, 5.0 mM) and stirred at 80° for 18 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, brine, dried (magnesium sulfate) and evaporated to a gum which was purified by MPLC on silica eluting with a gradient from 0 to 20% acetonitrile in ethyl acetate. Evaporation of appropriate fractions gave the title compound (719 mg) after trituration with diethyl ether. M&JBSE): 452(MH0toCMHaFaN5O2 NMR(DMSO-d£) 5: 2.30 (s,2H); 2.61 (s,2H); 3.05 (d,2H); 3.69 (s,2H); 3.80 (do, IH); 4.20 (t, IH); 4.60 (m, 2H); 5.09 (m, IH); 5.80 (s, IH); 7.30 (m, 7H); 6.99 (s, IH); 8.56 (s, IH). Example 61: (5RV3-(4~Cl .2.5.6-Tetrahydropyridm^-vIV3.5-diflaorophenylV5-Q.2.4-triazol-l-vlmethyl)oxazolidiii-2-one (5i?)-3 /lmethyl)oxazolidin-2-one one (631 mg, 1.4 mM) was reacted by essentially the technique of Example 46, to give the desired product as its hydrochloride salt (401 mg). VtS (ESP): 362 (MHO for C17H17F2N502 ^VTR fDMSO-dJ 5: 2.55 (overlapping DMSO, ~2H); 3.25 (overlapping H20,~2H); 3.73 (s,2H); 3.9(dd, IH); 4.17 (t, IH); 4.60 (t,2H); 5.10 (m,lH); 5.87 (s, IH); 7.27 (d, 2H); 7.98 (s, IH); 8.55 (s, IH); 9.23 (s, 2H); +1H for HC1 salt Example 62: f5JgV3-r4-n-rf4iy>-2.2-DimethvM.3-dioYo]ane-4-carbonv1V1.2.^.fi-tetrahydropvridin-4-yn-3.5-difluorophenylV5-n .2.4-triazoI-l -vlmethvnnyazoIidin-2-one (5i0-M4 oxazolidni-2-one hydrochloride (399 mg, 1.0 mM) was reacted by essentially the technique of Example 53, except that purification by MPLC on silica eluting with 5% methanol in dichloromethane was needed, to give the desired product (288 mg). MS (ESP): 490 (MH) for CJJH^FJNA NMR(DMSO-de) 8: 1.32 (d, 6H); 2.35 (m,2H); 3.70 (m, 2H); 3.90(dd,lH); 3.95-4.30. (complex, 5H); 4.60 (m, 2H); 4.88 (m, IH); 5.10 (m, IH); 5.85 (s, IH); 7.25 (d, 2H); 7.98 (s, IH); 8.55 (s, IH). Example 63: (5RV3-(4-n -rr2V)-2.3-Dihydroxvpropionvn-1.2.5.6-tetrahvdropvridin-4-yI)-3.5-diflnorophenyIV5-(1.2.4-triazoI-l-ylmethyl)oxazoHdiii-2-one (5i?)-3-(4-(l-((^,S)-2,2-Dimemyl-l,3-dioxolane-4-carbonyl)-l,2,5,64etrahydropyridm-4-yl)-3,5-difluorophenyl)-5-(l,2,4-triazol-l-y]methyl)oxazolidin-2-one (269 mg, 0.55 mM) was reacted by essentially the technique of Example 54, to give the desired product (130 mg). MS (ESP): 450 (MH+) for C^F^C^ NMR rDMSO-d^ 6: 2.35 (m,2H); 3.52 (m,2H); 3.72 (br,2H); 3.92 (dd, IH); 4.00-4.45 (complex, 4H); 4.65 (m, 3H); 4.98 (m, IH); 5.15 (m, IH); 5.90 (s, IH); 7.30 (d,2H); 8.00 (s, IH); 8.55 (s, IH). Example 64: (5J?)-3-(4-(1 -rf2J?V2-Hvdroxy-3-methylthiopropionvn-1.2.5.6-tetrahvdropvridin-4-yn-3-flTiorophenyl)-5-a.2.3-triazol-1-ylmethyI)oxazolidin-2-one (5i?)-3-(4-(l,2,5,6-Tetrahydropyridm-4-yl-3-fiuorophenyl)-5-(l,2,3-triazol-l-ylmethyl)-oxazohdin-2-one hydrochloride (400 mg, 1.05 mM), (2J2)-2-hydroxy-3-methylthiopropionic acid (143 mg, 1.05 mM; WO 92-00276), l~hydroxybenzotriazole (184 mg, 1.37 mM) and A^A^-diisopropylemylamine (177 mg, 1.37 mM) were dissolved in dichloromethane (10 ml) and l-(3-dimemylammopropyl)-3-emylcarbodiimide hydrochloride (263 mg, 1.37 mM) was added portionwise, and the mixture was stirred overnight. Solvent was removed and crude product purified by flash chromatography on silica eluting with 2% methanol in dichloromethane, to afford the title compound as a clear oil that readily crystallised (480 mg). MSJ£S£): 462(MH^forC2IH24FN504S NMRtoMSO-d^ 8: 2.10 (s, 3H); 2.43 (m, 2H); 2.61 (m, IH); 2.78 (m, IH); 3.65 (m, 2H); 3.90 (m, IH); 4.17 (m, 2H); 4.24 (t, IH); 4.50 (m, IH); 4.84 (d, 2H); 5.15 (m, IH); 5.44 (dd, IH); 6.03 (s, IH); 7.20-7.45 (m, 3H); 7.77 (s, IH); 8.17 s, IH). Example 65: (5R)-3-(4-(l -^J?)-2-Hvdroxy-3-methanesuIfonvIpropionyn-1.2.5.6-tetrahvdropyridin-4-vn-3-flnornphenvIV5-fl.2.3-triazoI-l-ylmethynoxazolidiii-2-one (5iO-3-(4-(l-((2i2)-2-Hydroxy-3-memylth^ fluorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazoUdin-2-one (430 mg, 0.93 mM) was stirred in dichloromethane (15 ml) at 0°, and 3-chloroperoxybenzoic acid (70%, 456 mg, 1.87 mM) was added portionwise. The solution was stirred at 0° for 1 hour. Dichloromethane (50 ml) was added and the mixture washed with saturated aqueous sodium bicarbonate (50 ml), dried (magnesium sulfate) and evaporated. Crude product was purified by flash chromatography on silica eluting with 4% methanol in dichloromethane to give the title compound as a white solid (349 mg). MS rBSP): 494 (MH4) for C21H24FN506S NMR fDMSO-d^ 6: 2.18-4.23 (m, 8H); 3.03 (s, 3H); 3.92 (m, IH); 4.23 (t, IH); 4.78 (m, IH); 4.83 (d, 2H); 5.14 (m, IH); 6.02 (dd, IH); 6.04 (s, IH); 7.20-7.46 (m, 3H); 7.75 (s, IH); 8.17 (s, IH). Example 66: (5^-3-r4-a-BenzyI-t.2.5.6-tetrahydropyridiii-4-yn-3-flnorophenyn-5'(2-oxo-3J?">-1.3-oxazol-3-yImethyl)nyazolidin-2-one (5i?)-3-(4-(l -Benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3 -fluorophenyl>5-hydroxymethyl-oxazolidin-2-one (2.92 g, 7.3 mM; WO 97-30995) was stirred in tetrahydrofuran (60 ml), and 3#-oxazol-2-one (0.69 g, 8.12 mM) and {ributylphosphine (1.77 g, 8.75 mM) were added. The mixture was stirred at 0° under nitrogen, and lsr-azodicarbonyldipiperidme (2.06 g, 8.18 mM) was added portionwise. The reaction mixture was allowed to warm to ambient temperature and stirred overnight. The precipitate was filtered off and solvent removed. The resulting oil was dissolved in dichloromethane (30 ml), stirred at 0° for 30 minutes, and further precipitate removed. The filtrate was purified by MPLC on silica eluting with a gradient from 60 to 80% ethyl acetate in wohexane, to give a mixture of starting material and product, which was rechromatographed eluting with 3% MeOH in dichloromethane to give the title compound as a white solid (30 mg). MS (ESP): 468 (MET) for QsH^NA Wm rDMSQ-d^ 5: 2.28 (m, 2H); 2.62 (t, 2H); 3.04 (m, 2H); 3.57 (s, 2H); 3.78-3.95 (m, 3H); 4.17 (t, 1H); 4.96 (m, 1H); 5.78 (s, 1H); 7.07 (d, 1H) 7.19 (d, 1H); 7.21-7.35 (m, 7H). Example 67: r51y)-3-r4-r3.6-Dihvdro-2g-pvran-4-vIV3-fluorophenvn-5-r2-oyo-1 H-pyridin-l-ylmethyI)oxazolidin-2-one 2-Hydroxypyridine (108 mg, 1.14 mM) was added at room temperature, under an atmosphere of nitrogen, to a stirred suspension of sodium hydride (60% dispersion in oil, 48 mg, 1.2 mM) in Ay^-dimethylformamide (5 ml). The reaction was stirred for 30 minutes then (i/2)-3-(4-(336-dihydro-2^-pyran-4-yl)-3-fluorophenyl)-5-memanesulfonyloxymemyloxazoUdin-2-one (400 mg, 1.08 mM; WO 97-09328) was added in one portion. The mixture was stirred and heated at 60° for 5 hour before quenching in water (20 ml) and extracting with ethyl acetate. The extract was washed twice with water and once with saturated brine, dried (magnesium sulfate) and evaporated to an orange oil, which was purified by flash chromatography on silica, eluting with 2.5% methanol in dichloromethane to give the title compound (115 mg) as a colourless solid. MS fESP): 371 (MIT) for C10H19FN2O4 NMR (CDC\) 5: 2.50 (m, 2H); 3.90 (m, 3H); 4.15 (t, 1H); 4.22 (dd, 1H); 4.31 (m, 2H); 4.46 (dd, 1H); 5.17 (m, 1H); 6.06 (m, 1H); 6.25 (t, 1H); 6.60 (d, 1H); 7.14 (dd, 1H); 7.26 (t, 1H); 7,30-7.45 (m, 3H). Example 68: r5igV3-r4-f3.6-Dihvdro-2g-pvran-4-yn-3-fluorophenyn-5-f2-oxo-2Jy-pyridaz-l»yImethyI)oxazolidin-2-one Diisopropylazodicarboxylate (248 mg, 1.2 mM) was added at room temperature to (5i?)-3-(4-(3,6-dmydro-2iJ-pyran-4-yl)-3-fluorophenyl)-5-hydroxymethyloxazoHdin-2-one(300mg, 1.02 mM), 2#-pyridazin-3-one (118 mg, 1.22 mM) and triphenylphosphine (340 mg, 1.30 mM) in tetrahydrofuran (8 ml). The reaction was stirred for 30 minutes then solvent evaporated and the residue purified by flash chromatography on silica, eluting with a gradient from 0 to 10% methanol in ethyl acetate, to give the title compound as a colourless solid (219 mg). MS : 372 (MH1) for C19H18FN304 NMRfCDCl^ 8: 2.50 (m, 2H); 3.90 (t, 2H); 3.96 (d, IH); 4.12 (t, IH); 4.32 (m, 2H); 4.50 (dd, IH); 4.58 (dd, IH); 5.14 (m, IH); 6.05 (m, IH); 6.96 (dd, IH); 7.17-7.28 (m, 3H); 7.38 (dd, IH); 7.81 (m, IH). Example 69: C5i?V3-r4-fl-Benzy]-1.2.5.6-tetrahvdropvridiii-4-vn-3-fluorophenvn-5- (tetrazol-l-ylmethyl)oxazolidin-2-oneand(5J?)-3-f4-(l-Benzyl-1.2.5:.6-tetrahydropyridiii- 4-yfl-3-fluorophenyI)-5-(tetrazol-2-yImethyftoxazoIidin-2-one Diethylazodicarboxylate (2.28 g, 13.1 mM) was added, under an atmosphere of nitrogen, to a mixture of (5iZ)-3-(4-(l-benzyl-l,2,5364etrahydropyiidin-4-yl)-3-fluorophenyl)-5- hydroxymethyloxazoHdin-2-one (5.0 g, 13.1 mM; WO 97-30995), l#-tetrazole (0.91 g, 13.0 mM) and rriphenylphosphine (3.43 g, 13.1 mM) in tetrahydrofuran (150 ml), pre-cooled in ice/water. The reaction was then allowed to warm to room temperature and stirred 18 hours. Solvent was evaporated and the resulting brown oil dissolved in dichloromethane (80 ml) and cooled in ice/water before filtering. The filtered solution was purified by MPLC on silica, eluting with ethyl acetate to give the title compounds; the 2-tetrazole isomer is the less polar, and elutes first. Each was then individually purified by strong cation ion-exchange chromatography (10 g Bond Elut®), elutmg with a gradient from 0 to 5% methanol in dichloromethane, followed by 3% 880 ammonia in a 9:1 mixture of dichloromethane and methanol, to give 2-tetrazole (2.61 g) and 1-tetrazole isomers (0.44 g) as colourless solids. 2-Tetrazole: MS ffiSPl- 435 (MH) for C^FNA NMR(DMSO-d^ 6: 2.42 (m, 2H); 2.60 (t, 2H), 3.05 (d, 2H), 3.58 (s, 2H); 3.91 (dd, IH); 4.30 (t, IH); 5.11-5.31 (m, 3H); 5.97 (m, IH); 7.19-7.44 (m, 8H); 9.01 (s, IH). 1-Tetrazole: MS (ESP): 435 (MH1) for C^FNA NMR (DMSO-d^ 5: 2.43 (m,2H); 2.60 (t,2H); 3.04 (d, 2H); 3.58 (s,2H); 3.92 (dd, IH); 4.25 (t, IH); 4.93 (d, 2H); 5.17 (m, IH); 5.97 (m, IH); 7.19-7.44 (m, 8H); 9.48 (s, IH). Example 70: f5J?V3-r4-fl.2.5.6-Tetrahvdropyridin-4-vn-3-fluorophenvn-5-ftetr27n1-2-ylmethvfloxazoIidin-2-one 1-Chloroetbyl chloroformate (1,18 g, 8.3 mM) was added dropwise, under an atmosphere of nitrogen, to a stirred solution of (5i?)-3-(4-(l-ben2yl-l,2,5564etrahydropyridin-4-yl)-3-fluoro-phenyl)-5-(tetrazol-2-ylmethyl)oxazoUdin-2-one (2.56 g, 5.90 mM) and T^TV'-dusopropylemylamine (0.230 mg, 1.77 mM) in dichloromethane (50 ml) with cooling in ice/water. The reaction was stirred for 30 minutes at ice temperature, and the brown solution purified by MPLC on silica, eluting with 75% ethyl acetate in zsohexane. The resulting carbamate intermediate was dissolved in methanol (60 ml) and heated at 60° for 30 minutes. Evaporation of the solvent and trituration with diethyl ether gave the title compound (1.76 g) as its hydrochloride salt. MS fBSP): 345 (MH4) for ClfiH17FN602 NMR fDMSO-d^ 8: 2.65 (s, 2H); 3.28 (t, 2H); 3.72 (d, 2H); 3.92 (dd, IH); 4.30 (t, IH); 5.11-5.32 (m, 3H); 6.03 (m, IH); 7.28 (m, IH); 7.38-7.50 (m, 2H); 9.05 (s, IH); 9.30 (br s; 2H). Example 71: f5/?KW4-fl-f(4Vl2.2-Dimethvl-1.3-dioxolane-4-carbonvn-1.2.5.6-tetrahydropyridin-4--vlV3-fluorophenvlV5-(tetrazol-2-ylmethvI)oxazoHdip-2-one (^5)-2,2-Dimethyl-l,3-dioxolane-4-carbonyl chloride (350 mg, 2.10 mM) was added dropwise to a stirred suspension of (5i2)-3-(4-(l,2,5,6-tetrahydropyridin-4-yl)-3-fluoro-phenyl)-5-(tetrazol-2-ylmethyl)oxazolidin-2-one hydrochloride (500 mg, 1.31 mM) and pyridine (0.52 g, 6.57 mM) in dichloromethane (20 ml) with ice/water cooling. The reaction was allowed to warm to room temperature and stirred 1 hour. The resulting solution was washed with water and saturated brine, dried (magnesium sulfate) and evaporated to a small volume. Addition of diethyl ether gave the title compound (600 mg) as a yellow solid. MS (ESP)'. 473 (MET) for C^H^FNA NMR (DMSO- Example 72: f5i?V3-f4-fl-(1-Ac.Ptnxyacetyl)-l.2.5.6-tetrahydropvridm-4-vlV3-flTinrn-phenyIV5-ftetrazoI-2-vImethvI)nxazolidm-2-one Acetoxyacetyl choride (0.356 mg, 2.63 mM) was added dropwise to a stirred solution of (5R)~ 3-(4-(l,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-(tetrazol-2-ylmethyl)oxa^ hydrochloride (500 mg, 1.31 mM) and sodium hydrogen carbonate (1.10 g, 13.1 mM) in a mixture of water (10 ml) and acetone (20 ml) with ice/water cooling. The reaction was allowed to warm to room temperature and stirred 16 hours, then diluted with water (80 ml) and extracted with ethyl acetate (3 x 80 ml). The combined extracts were washed with saturated brine, dried (magnesium sulfate) and evaporated to a yellow oil. Trituration with diethyl ether gave the title compound as a yellow solid (390 mg). MS (ESP): 445 (MH) for C20H21FN6O5 NMR (DMSO-d^ 5: 2.10 (s,3H); 2.42 (partly obscured by DMSO, 2H); 3.51-3.68 (m,2H); 3.94 (dd, 1H); 4.09 (m, 2H); 4.29 (t, 1H); 4.82 (m, 2H); 5.10-5.30 (m, 3H); 6.00 (m, 1H); 7.24 (m, 1H); 7.35-7.49 (m, 2H); 9.02 (s, 1H). Example 73: (5K)-3-(4-(l-((2S\-2.1-Dihydroxvpropionyn-1.2.5.6-tetrahvdrnpvridin-4-yl)-3-fluorophenyI)-5-(tetrazoI~2-ylmethyI)oxazoIidin-2-one (5i?)-3-(4-(l-((4S)-2,2-Dimetoyl-l^ fluorophenyl)-5-(tetrazol-2-ylmethyl)oxazolidin-2-one (550 mg, 1.17 mM) in a mixture of tetrahydrofuran (25 ml) and aqueous hydrochloric acid (1M, 10 ml) was stirred at room temperature for 24 hours, then concentrated by evaporation to a solid. The solid was filtered, washed with water, followed by a small volume of ethanoL, then triturated with diethyl ether to give the title compound as a colourless solid (450 mg). MS (ESP): 433(Mrr)forC19H21FN605 NMK rDMSO-d^ 8: 2.41 (partly obscured by DMSO, 2H); 3.41-4.42 (m, UK); 5.11-5.32 (m, 3H); 6.01 (m, 1H); 7.25 (m, 1H); 7.35-7.48 (m, 2H); 9.04 (s, 1H). Eyample 74: r5JgV3-f4-tt-(2-HvriroYvar.etvn-1.2.5.6-tetrahydropvridin-4-yI)-3-fluoro-ph enylV 5-ftetrazol-2-yImeth vl WazoIidin-2-on e '5#)-3-(4-(i-(2-Acetoxyacetyl)-l,2,5,6-tetrahydr^ ^lmethyl)oxazolidin-2-one (365 mg, 0.82 mM) was treated with a saturated solution of ammonia in methanol (40 ml), warmed slightly to dissolve completely, then stirred at room temperature for 20 hours. The solvent was evaporated to give an orange oil which was triturated with diethyl ether to give the title compound as a pale yellow solid (211 mg). MS (ESP): 403 (MET) for.ClgH19FNfi04 NMR (DMSO-dg) 5: 2.45 (partly obscured by DMSO, 2H); 3.50-3.70 (m, 2H); 3.92 (dd, IH); 4.03-4.19 (m, 4H); 4.30 (t, IH); 4.55-4.65 (m, IH); 5.10-5.31 (m, 3H); 5.95-6.04 (m, IH); 7.23 (m, IH); 7.34-7.48 (m, 2H); 9.04 (s, IH). .1 Example 75: r5/?V3-f3.5-Diflaoro-4-(3.6-dihvdro-l.l-dioxo-2/y-thiopvran-4-ynpheny1V 5-ttetrazoI-l -ylmethvIWaznlidm-2-one and f5^-3-f3.5-Difluoro-4-f3.6-dihvdro-l .1 -dioxo-2.H'-thiopyran-4-yl)phenvr>-5-ftetrazol-2-yImethvnoxazolidin-2-one (Ji?)-3-(3,5-Difluoro-4-(256-d^ydro-14-dUoxo-2^-tmopyran-4-yl)phenyl)-5-memane- sulfonyloxymethyloxazolidin-2-one (437 mg, 1 mM), was treated with IH-tetrazole (105 mg, 1.5 mM) essentially as in Example 34 except that the mixture was heated to 75° for 2 hours. Crude product after the ethyl acetate extraction was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 100% ethyl acetate in dichloromethane. Relevant fractions of the first eluting product were combined to give the less polar tetrazol-2-yl isomer (206 mg). MS (ESP): 412(MH+)forC16HJ5F2Ns04S NMR (DMSO-d^) 5: 2.82 (m,2H); 3.32 (m overlapped by H20,~2H); 3.93 (overlapping m, 3H); 4.28 (t, IB); 5.15 (d, IH); 5.24 (d, IH);. 5.30 (m, IH); 5.75 (br s, IH); 7.31 (d, 2H); 9.03 (s, IH). The second eluting product was the 1-isomer (105 mg). MSJCESE): 412 (MET) for Cl6El5F2^504S NMR (DMSO-d_5) 5: 2.81 (m,2H); 3.33 (m overlapped by H20, ~2H); 3.92 (overlapping m, 3H); 4.26 (t, IH); 4.93 (d, 2H); 5.18 (m, IH); 5.74 (s, IH); 7.31 (d, 2H); 9.48 (s, IH)-. Example 76: (5J?V3-(4-n -TsnpropylsuIfonyl-1.2.5.6-tetrahydropyridin-4-vI)-3-fhioro-phenyIV5-(1.2.3-rria?:nl-t -ylmpithyDoxazolidm-2-one (5i?)-3-(4-(l}2s5}6-Tetrahydropyridm-4-yl)-3-fluorophenyl)-5-(l5253-triazol-l-ylme%l)-oxazolidin-2-one hydrochloride (380 mg, 1 mM) was dissolved in water (5 ml), which was then diluted with acetone (10 ml), and solid sodium bicarbonate (0.84 g, 10 mM) added. The mixture was stirred and cooled to 0°C, and isopropylsulfonyl chloride (285 mg, 2 mM) added dropwise. After stirring for 5 hours, an equal portion of sulfonyl chloride was added, and stirring continued for 18 hours. Most acetone was removed by evaporation, the residue diluted with water (50 ml), and extracted with ethyl acetate (3 x 20 ml). The extracts were washed with brine and dried (magnesium sulfate). The residual oil after evaporation was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (205 mg). MS (ESP): 450 (MET) for C^FN^S NMRftDHj) 8: 1.37 (d, 6H); 2.53 (br, 2H); 3.22 (heptet, 1H); 3.56 (td, 2H); 3.94 (dd, 1H); 4.03 (m, 2H); 4.16 (t, 1H); 4.78 (d, 2H); 5.06 (m, 1H); 5.92 (m, 1H); 7.07 (dd, 1H); 7.19 (td, 1H); 7.29 (dd, 1H); 7.74 (d, 1H); 7.78 (d, IF). Example 77: f5J?^3-r4-ri-Methvlsulfonyl-1.2.5.6-tetrahvdropyridin-4-ylV3-flnoro-phenvl)-5-(1.2.3-triazol-l-ylmethyl)oxazolidm-2-one (5i2)-3-(4-(l,2,5,6-Terrahydropyridm-4-yl)0-fluorophenyl)-5-(l,2,3-triazol-l-ylme^ oxazolidin-2-one hydrochloride (380 mg,-1 mM) was suspended in dichloromethane (15 ml), 4-d^emylaminopyridine (305 mg, 2.5 mM) added, and the mixture stirred vigorously for 15 minutes. After cooling to 0°C under nitrogen, methanesulfonyl chloride (229 mg, 2 mM) was added dropwise, and the mixture stirred 18 hours at ambient temperature. Precipitated solid was removed, and the organic solution concentrated, then purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (30 mg). MSiESE): 422 (MIT) for C18H20FN5O4S NMRfDMSO-d^ 5: 2.52 (br, 2H); 2.92 (s, 3H); 3.34 (t, 2H); 3.84 (m, 2H); 3.89 (dd, 1H); 4.23 (t, 1H); 4.82 (d, 2H); 6.01 (br, 1H); 7.23 (dd, 1H); 7.36 (t, 1H); 7.40 (dd, 1H); 7.74 (d, 1H); 8.14 (d, 1H). Example 78: riigl-S-M-n-EtliylsulfonvI-l.Z.S.g-tetrahydropyridin^-yn-S-fluorophenyn-5-(1.2.3-triazol-l-yImethvr>oxazoIidin-2-one (5i?)-3^4-(l,2,5,6-Tetrahydropyridm-4-yl)-3-fluorophenyl)-5 NMR (CDCy 5: 1.39 (t, 3H); 2,55 (br, 2H); 3.02 (q,2H); 3.53 (t,2H); 3.94(dd,lH); 3.99 (m, 2H); 4.16 (t, IH); 4.78 (d, 2H); 5.06 (m, IH); 5.92 (br, IH); 7.06 (dd, IH); 7.19 (t, IH); 7.29 (dd, IH); 7.74 (d, IH); 7.78 (d, IH). Example 79: (5SW-(4-(1 -TrifliioromethyIsnlfonvI-1.2.5.6-tetrahvdropyridin-4-yn-3-flnorophenyn-5"fl.2.3-triazol-1-ylmethyl)oxazolidin"2"0ne (5J?)-3-(4-(l,2,5,6-Tetrahydropyrio^"4-yl)-3"fluorophenyl)-5-(l,2,3-Mazol-l-ylmemyl)-oxazolidin-2-one hydrochloride (380 mg, 1 mM) was treated with trifluoromethanesulfonyl chloride essentially as in Example 76. Crude material was purified by chromatography on a 5 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 10% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (444 mg). MS (ESP): 476 (MIT) for C,8H17F4N504S NMR rDMSO-d,') 5: 2.55 (br, 2H); 3.71 (t, 2H); 3.88 (dd, IH); 4.16 (m, 2H); 4.23 (t, IH); 4.81 (d,2H); 5.13 (m, IH); 6.02(br,lH); 7.24 (dd, IH); 7.38 (t, IH); 7.42(dd,lH); 7.74 (d, IH); 8.14 (d, IH). Example 80: f5JgV3-r4-ri-f3-Ch1oropropvnsulfonyl-1.2.5.6-tetrahvdrnpvridm-4-vD~3-fluorophenv1V5-n.2.3-triazol-l-vlmethvnnxazoIidin-2-one (5i?)-3 NMR rDMSO-d.) 8: 2.12 (quintet, 2H); 2.49 (br, obscured by DMSO,~2H); 3.21 (t,2H); 3.42 (t,2H); 3.73 (t,2H); 3.89 (overlapping m,3H); 4.23 (t, IH); 4.82 (d,2H); 5.13 (m, IE); 6.01 (br, 1H); 7.23 (dd, 1H); 7.35 (t, 1H); 7.41 (dd, IE); 7.74 (d, 1H); 8.14 (d51H). Example 81: r5gV3-r4-fl-f2-MethoxyethvnsnlfonvI-1.2.5.6-tetrahvdropvridin-4-yn-^-fluorophenvn-5-n.2.3-triazoI-l-ylmethynoxazoIidm-2-oiie (JJ?)-3-(4-(l,2,5,6-Tetraliydropy^ oxazolidin-2-one hydrochloride (380 mg, 1 mM) was treated with 2-methoxyethylsulfonyl chloride essentially as in Example 79. Chromatography gave the desired product (65 mg). MS fESP): 466 (MET) for C20H24FN505S NMRCCDCI^ 8: 2.55 (br, 2H); 3.25 (t, 2H); 3.37 (s, 3H); 3.50 (t, 2H); 3.77 (t, 2H); 3.92 (m, 1H); 3.97 (m, 2H); 4.16 (t, IE); 4.78 (d, 2H); 5.06 (m, 1H); 5.91 (br, 1H); 7.06 (dd, IB); 7.18 (t, 1H); 7.29 (dd, 1H); 7.74 (d, 1H); 7.78 (d, 1H). Example 82 : f5i?V3-r3-FIuoro-4-(;/ (J^-S-^S^-dmydro^H-thiopyran^-yO-S-fluorophenyll-S^l^^-triazol-l-ylmethyl)oxazolidin-2-one (Example 83; 1.25 g, 3.5 mmol) was stirred in a mixture of methanol and ethyl acetate (1:1, 50 ml) at ambient temperature. Sodium periodate (0.93 g, 4.3 mmol) in water (10 ml) was added dropwise, and it was stirred for 18 hours. Precipitated salts were removed by filtration and solvents were removed under vacuum. The residue was chromatographed on silica gel, washing with 25% acetone in dichloromethane, then eluting with 5 to 7% methanol in dichloromethane to give the title product (1.152 g). MS (ES?): 377 (MIT) for C17HnKNAS Lff-NMR fDMSO-dfr) 8: 2.57 (m, 1H); 2.91 (m, 1H); 2.97 (m, 1H); 3.13 (m, 1H); 3.39 (m, 1H); 3.67 (m, 1H); 3.92 (dd, 1H); 4.27 (dd, 1H); 4.86 (m, 2H); 5.17 (m, 1H); 5.84 (m, 1H); 7.28 (dd, IK); 7.39 (dd, 1H); 7.45 (dd, 1H); 7.79 (d, 1H); 8.20 (d, 1H). Example 83 : f5JgV3-f4-r3.6-dihydro-2g-thiopyran-4-v1V^-fliinrophenyl]-5-fl.2.3-triazoI-l-vlmethyl)oxazolidin-2-one (5J?)-3-[4-(3,6-dmydro~2#-fluopy^^ (2g, 5.7 mmol) was dissolved in dioxane (10 ml). BicycIo[2.2.1]hepta-2,5-diene (3.1 ml, 28.7 mmol) was added and it was refluxed under nitrogen for 18 hours. The solvent was evaporated in vacuo and the residue subjected to chromatography on silica gel eluting with 25% ethylacetate in dichloromethane to give the title compound (1.51 g). MS (ESP): 361 (MIT) for C17H17FN402S J-H-NMR fDMSO-d£> 5: 2.56 (m, 2H); 2.83 (dd, 2H); 3.31 (m, 2H); 3.91 (dd, IH); 4.26 (dd, IH); 4.86 (m, 2H); 5.17 (m, IH); 6.06(m, IH); 7.25 (dd, IH); 7.33 (dd, IH); 7.42 (dd, IH); 7.78 (d, IH); 8.19 (d, IH). The above Examples 82 & 83 were prepared from the intermediates below: (5i?V3-[4-(3.6-dihvdro-2i7-tMopwaTi^v1V3-fluorophenvl]-5-azidomethvloxa7olidin-2-one Metbanesulfomc acid (5i?)-3-[4-(3,6-dih^^ oxazolidin-5-ylmethyl ester (8 g, 19.7 mmol) and sodium azide (4 g, 61.5 mmol) were heated in N,N-dimethylformarnide (75 ml) at 80°C for 2 hours. It was cooled to room temperature, diluted with ethyl acetate, washed with potassium phosphate buffer (pH 7) and with water and dried over sodium sulfate. After evaporation of the solvent the title product was obtained as a brown oil (~7 g, crude). iH-NMR (DMSO-d^) 5: 2.56 (m, 2H); 2.83(dd,2H); 3.31 (m,2H); 3.71 (dd, IH); 3.80 (dd,lH); 3.81 (dd, IH); 4.17(dd,lH); 4.92 (m, IH); 6.06(m, IH); 7.34 (m,2H); 7.50 (m, IH). Methanesulfomcacid(5J?)-3-[4-(3.6-dihydro-2i7-thiopyran-4-yl)-3-fluorop\|ienyI]-2-oxo-oxazolidm-5-vlmethvl ester (5i?)-3-[4-(3,6-dihydro-2F-tMopyran^-yl)-3-3Quorophenyl]-5-hydroxymethyloxazoUdin-2-one (14 g, 45.3 mmol) was dissolved in dichloromethane (300 ml) and triethylamine (8.8 ml, 63.3 mmol) was added. It was cooled to -20°C and methanesulfonyl chloride (4.22 ml, 54.4 mmol), dissolved in dichloromethane (50 ml), was added dropwise. The reaction mixture was allowed to warm to room temperature and was quenched with potassium phosphate buffer (pH 7). Dichloromethane was removed under vacuum and it was extracted with ethyl acetate, washed with water and dried over magnesium sulfate. The title compound (16.9 g) was precipitated from dichloromethane by addition of hexane. ^-NTVTR rPMSO-d^ 5: 2.56 (m, 2H); 2.83 (dd, 2H); 3.28 (s, 3H); 3.32 (m, 2H); 3.85 (dd, 1H); 4.21 (dd, 1H); 4.48 (dd, 1H); 4.53 (dd, 1H); 5.04 (m, 1H); 6.07 (m, 1H); 7.33 (dd, 1H); 7.36 (dd, 1H); 7.50 (dd, 1H). (5i?)-344-(3-6-dihvdro-2F-thiopyran-4-yl)-3-fluorophenv1]-5-hvdroxvmethvloxa7o1idm-2- sns 4-(2-Fluoro^benzyloxycarbonylammophenyl)-3,6-dmydro-2i^tbiopyran (15.3 g, 44.6 mM) was dissolved in dry tetrahydrofuran (175ml) and stirred under nitrogen at -70°C. n-ButylUthium (1.6M in hexanes, 30ml, 175 mM) was run in over 20 minutes, keeping the temperature below -60°, and the mixture then stirred a further 10 minutes at -70°C. A solution of (iJ)-glycidyl butyrate (6.42 g, 44.62 mM) dissolved in dry tetrahydrofuran (10 ml) was added dropwise over 10 minutes keeping temperature below -60°, and the mixture left to warm to ambient temperature over 18 hours. Methanol (29ml) was added, and the mixture stirred for 10 minutes only. Saturated aqueous sodium bicarbonate (200 ml) was added, and the mixture extracted with ethyl acetate (400 ml). The extract was washed with saturated aqueous sodium bicarbonate (100ml), brine (100ml), dried (magnesium sulfate). Filtered and evaporated. The crude product was purified on a 300 g silica sinter column, eluting with a gradient from 0% to 100% ethyl acetate in dichloromethane. Relevant fractions were combined, reduced to a small volume, and diluted with an excess of is^hexane to precipitate the desired product (11.3 g). MS (ESP): 310 (MIT) for C15H16FN03S NMR rDMSO-d^ 6: 2.52 (m overlapped by DMSO,~2H); 2.78 (t,2H); 3.27 (m, 2H); 3.52 (m, IB); 3.65 (m, 1H); 3.80 (dd, 1H); 4.06 (dd, 1H); 4.65 (m, 1H); 5.19 (t, 1H); 6.01 (s, 1H); 7.28 (m, 2H); 7.47 (dd, 1H). 4-(2-Fluoro-4-benzyloxvcarhonvlaminophenvD-3.6-dihvdro-2g-thiopvran 4-(2-Fluoro-4-arm^ophenyl)-3,6-dihydro-2fl-thiopyran (9.8 g, 46.8 rnM) was dissolved in dry dichloromethane (196ml), pyridine (6.23g, 79.1 mM) added, and the mixture stirred under nitrogen at -20°. A solution of benzyl chloroformate (9.54g, 53.9 mM) dissolved in dry dichloromethane (25 ml) was added dropwise, and the mixture left to warm to ambient temperature over 18 hours. The mixture was washed with 1M hydrochloric acid (200 ml), then brine (100 ml), dried (magnesium sulfate), filtered and evaporated to a small volume. The addition of wohexane (300 ml) precipitated the desired product (15.5 g). MS (Negative ESP): 342 (M-H) for C19HI8FN02S NMR (DMSO-dgl 5: 2.50 (s,2H); 2.79 (t,2H); 3.26 (m,2H); 5.15 (s,2H); 5.99 (s, 1H); 7.18 (m, 2H); 7.38 (m, 6H); 10.01 (s, 1H). 4-(2-Fluoro-4-aminophenyl)-3.6-dihydro-2/f-thiopyran 4-Hya^oxy-4-(2-fluoro-4-aminophenyl)tetrahydrothiopyran (11.35 g, 50 mM) and butylated hydroxytoluene (50 mg) as antioxidant were suspended in a mixture of concentrated hydrochloric acid (37%, 200 ml) and water (50 ml), and stirred at 80° under nitrogen for 18 hours. Glacial acetic acid (150 ml) was added, and reaction continued at 80° for a further 5 hours. After cooling, the reaction was made basic by the cautious addition of concentrated ammonia and ice. The mixture was extracted with diethyl ether (400 ml), the extract washed with water (100 ml), brine (100 ml), dried (magnesium sulfate), filtered and evaporated to give the title product (10 g) as a dark oil. NMR (CPCIj) S: 2.59 (m,2H); 2.72 (t,2H); 3.30 (m,2H); 3.80 (far, 2H); 5.93 (m, IH); 6.35 (dd, IH); 6.39 (dd, IH); 6.97 (t, IH). Example 84 : (5JgV3-f4-a.l-dioxo-3.6-dihydro-2H-thiopvrap-4-vn-^-fliinrophenvI\|-5-fl.2.3-triazo1-l-vlmetfaynoxazoIidiii-2-oiie (5^)-3-[4 2H); 5.18 (m, IH); 5.83 (m, IH); 7.29 (dd, IH); 7.40 (dd, IH); 7.47 (dd, IH); 7.78 (s, IH); 8.19 (s, IH). Example 85: r5i?V3-r^.f;-T)ifliinrn-4-(7fg.ty)-OYo-3.6-dihvdro-2H-thiopvran-4-yIV phenyI]-5-ri.2.3-triazol-l-vImt>thvDoxazoIidin-2-one (5i?)-3-[4-(3,6-dihydro-2^thiopyran-4-yl)-3,5-chfluorophenyl]-5-(l,233-triazol-l-ylmethyl)oxazolidin-2-one (Example 86; 0.86 g, 2.3 mmol) was stirred in a mixture of methanol and ethyl acetate (1:1,20 ml) at ambient temperature. Sodium periodate (0.50 g, 2.4 mmol) in water (10 ml) was added dropwise, and the mixture stirred for 3 hours. Precipitated salts were removed by filtration and washed with ethyl acetate. The filtrate was washed with brine, dried over magnesium sulfate and concentrated to dryness. The residue was chromatographed on silica gel eluting with 5% methanol in dichloromethane to give the title product (0.69 g). MS fESP): 395 (MHT) for C17HJ6F2N403S ^H-NMR fDMSO-d^ 5: 2.41 (brs, 1H); 2.80 (m, 1H); 2.97 (brs, 1H); 3.15 (m, 1H); 3.39 (m,lH); 3.67 (brs, 1H); 3.94 (m, 1H); 4.25 (dd, 1H); 4.85 (brs, 2H); 5.19 (m, 1H); 5.75 (brs, 1H); 7.33 (d, 2H); 7.79 (brs, 1H); 8.20 (brs, 1H). Example 86: r5i?)-3-f4-r3. Meftaaesulfomc acid (5i?)-3-[4-(3,6-dihy^ oxazohdin-5-ylmethyl ester (1.1 g, 5.7 mmol) was dissolved in dry N,N-dimethylformamide (5 ml) and sodium azide (0.35 g, 5.43 mmol) was added. It was heated at 60°C for 18 hours. The reaction mixture was cooled to room temperature, diluted with ethylacetate, washed with water and dried over magnesium sulfate. Solvent was removed under vacuum to give an oil. The crude intermediate azide was not characterized. It was taken up in 1,4-dioxane (20 ml), bicyclo[2.2.1]hepta-2,5-diene (1.0 g, 10.9 mmol) was added and it was refluxed for 12 hours. Solvent was removed under vacuum and the residue chromatographed on silica gel with 5% methanol in dichloromethane to give the title compound (0.62g). MS (ESP): 379 (MrT) for C17H1SF2N402S NMR (DMSO-d^) 8: 2.43 (brs, 2H); 2.83(dd,2H); 3.31. (brs, 2H); 3.92 (m, IH); 4.25 (dd, IH); 4.84 (d,2H); 5.18 (m, IH); 5.98 (brs, IH); 7.28 (d,2H); 7.79 (brs, IH); 8.19 (brs, IH). The above Examples 85 & 86 were prepared from the intermediates prepared analagously to those used in Examples 82 & 83. Example 87 :f5J?V3-f3r5-Diflnoro-4.fJr3?.,y)-oxo-3.6-dihvdro-2H-thiopvran-.4-yn-pheiivIl-5-(1.2.3-triazoI-2-yImethyI)oxazoIidin-2-one (5iJ)-3-[4 folH); 3.67 (brs, IH); 3.93 (m,lH); 4.26 (dd, IH); 4.88 (m,2H); 5.24(m, IH); 5.76 ^rd, IH); 7.31 (d,2H); 7.86 (s,2H). Example 88 : r5J?V3-[4-r3.6-dihydrn-2fl-thiopvran-4-vn-3.5-difluornphenvl\|^-n.'Z.^-triazol-2-yImetbyfloxazolidin~2-one Sodium hydride (60% in oil, 148 mg, 3.7 mmol) was suspended in dry N,N-dimethylformamide (5 ml) and 1,2,3-triazole (0.26 g, 3.7 mmol) was added under nitrogen. It was stirred for 5 minutes at room temperature and methanesulfonic acid (5i?)-3-[4-(3,6-dmydro-2/y-tm^pyran-4-yl)-3,5-difluorophenylJ-2-oxo-oxazoHdm-5-ylmethyl ester (see Example 86; 1.0 g, 2.47 mmol) was added. It was heated to 75°C for 3.5 hours, then cooled to room temperature, diluted with aqueous sodium hydrogencarbonate solution (5%, 100 ml) and extracted with ethylacetate (2 x 100 ml). The organic phase was washed with water (2 x 50 ml), brine (100 ml), dried over magnesium sulfate and the solvent was evaporated in vacuo. Chromatography on silica gel with a gradient of 10-50% ethylacetate in hexanes gave the title compound (0.65g). MS (ESP^: 379. (Mff) for C17H16F2N402S NMR (CDCL) 6: 2.53 (m, 2H); 2.89 (dd, 2H); 3.35 (m, 2H); 3.95 (m, 1H); 4.25 (dd, 1H); 4.83 (m, 2H); 5.09 (m, 1H); 5.96 (brs, 1H); 7.05 (d, 2H); 7.79 (d, 2H). Example 89: 5rRVf3-Oxo-isoxazo]-2^vlmethvlV3-r4-fl.2.f).6-tetrahvdropvrid-4-vn-3.5-difluorophenyI)oxazoIidin-2-one PCT Application No. GB99/01753 (Publication No. WO 99/64417) describes the preparation of 5(R)-Hydroxyme%l-3 During the Mitsunobu reaction the ambident nucleophile 3-hydroxyisoxazole reacts with S(R)-Hydroxymethyl-S^^Cl-benzyl^^^^-terrahydropyrid-^-yl)^^- difluorophenyl)oxazolidin-2-one to give a quantity of S^HS-Oxo-isoxazol^-ylmethylJ-S-^- fl-bei^M^S^etrahydropyrid^-yty-S^-difluoro^ Failure to purify (e.g. by suitable column chromatography) the product from the Mitsunobu reaction described in GB99/01753 before subsequent reaction with 1-chloroethyl chloroformate and work-up using hydrochloric acid gives a quantity of 5(R)-(3-Oxo-isoxazol-2-yhnethyl)-3-(4- (l^jSje-tetrahydropyrid^-ylJ-SjS-difluoropheny^oxazoHdin^-one as the hydrochloride salt, which is identified in the mixture by correlation TOCSY NMR (TOtal Correlation Spectroscopy) - methylene carbon attached to the nitrogen of the isoxazolone ring has a shift of 48 ppm (characteristic of this linkage), and by LC-MS (MH+ 378 - less chloride) using C- 18 Hichrom RPB column, 5mm, 25cm x 0.46mm i.d; Eluant - 650ml Water, 350ml Acetonitrile, 1ml TFA (biograde); Flow - 1.5ml/min; Retention Times N-linked Piperidene - Rt = 2.0 min, O-linked Piperidene - Rt = 3.25 min. ( -one To 3-tert-butoxy-2(S)-hydroxypropanoic acid (343 mmol) in dimethylformarnide (DMF) at iO-25°C was added (4-(l,2,5,6-tetrahydropyrid-4-yl)-3,5-difiuorophenyl)oxazoHdin-2-one lydrochloride salt (264 mmol; Reference Example 6 of GB99/01753, prepared as described in Example 89 without purification following the Mitsunobu reaction of 3-hydroxyisoxazole reacts with 5(R)-Hydroxymethyl-3-(4-(l-benzyl-1,2}5,6-tetrahydropyrid-4-yl)-3,5-&fluorophenyl)oxazolidin-2-one). To the mixture was added 1-hydroxybenzotriazole hydrate (HOBt; 0.4 eq.) and further DMF (to 6 vol.). The solution was placed under a nitrogen atmosphere, cooled to 16-18°C and Et3N (1.5 eq.) added. l-[3-(Dimethylamino)propyl]-3-ethylcarbodiirnide hydrochloride (EDO; 1.4 eq.) dissolved in water (1.5 vol.) was added dropwise keeping the temperature below 25°C. After approximately one hour the reaction :was complete and tert-butyl methylether (MTBE; 1 vol.) followed by water (12 vol.) was added. After vigorous stirring for 1 hour the resultant solid was filtered, washed with water and MTBE, and dried under vacuum at 35-40°C. The resultant product (3.71 kg) was dissolved in DCM (8.5 litres) and purified by column chromatography eluting with EtOAc/iso-hexane (80:20) collecting the appropriate fractions and removing the solvent under reduced pressure to give 5(R)-Isoxazol-3-yloxymethyl-3-(4-(l-(34ert-butoxy-2(S)-hydYoxypropanoyl)-l,2,5,6-tetrahydropyrid-4-yl)-3,5-difluorophenyl)oxazoUdin-2-one as a white foam (3.03 kg, 82% yield). The column was eluted further with methanol (50.5 litres) and the solvent removed under reduced pressure to give a brown gum (100 g). Trituration of the gum with EtOAc (500 ml) gave the title compound as a dark yellow solid (1 OOg). IR (KBr disk) (ran1) 1737 (CO, oxazolidinone), 1638 (CO, amide); MS (MH+) 522; JHNMR(500MHz) assigned via TOCSY and HMQC (Heteronuclear Multiple Quantum Coherence spectra - A 1H/13C correlation) - methylene carbon attached to the nitrogen of the isoxazolone ring has a shift of 49 ppm (characteristic of this linkage). Example 90 (5.0g) was slurried in 4M HC1 in dioxane (25ml) and stirred at ambient temperature for 24 hours. The gum that formed was washed with dioxane (20 ml) and triturated with isobutanol (50 ml). The solid that resulted was washed with isobutanol (2x10 ml) and dried under reduced pressure to give the title, compound as a yellow solid (3.4g). XH NMR (500MHz) assigned via TOCSY and HMQC correlation spectra. Methylene carbon attached to the nitrogen of the isoxazolone ring has a shift of 47 ppm (characteristic of this linkage vs O-linkage); MS (MH+) 466. Example 92 The following illustrate representative pharmaceutical dosage forms containing a compound of the formula (I), an in-vivo hydrolysable ester or a pharmaceutically-acceptable salt thereof, including a pharmaceutically-acceptable salt of an in-vivo hydrolysable ester, (hereafter compound X), for therapeutic or prophylactic use in humans: (a) Tablet I mg/tablet CompoundX 500 Lactose Ph.Eur 430 Croscarmellose sodium 40 Polyvinylpyrrolidone 20 Magnesium stearate 10 (b) Tablet n mg/tablet Compound X 100 Lactose Ph.Eur 179 Croscarmellose sodium 12 Polyvinylpyrrolidone 6 Magnesium stearate 3 (c) Tablet HI mg/tablet CompoundX 50 Lactose PLEur. 229 Croscarmellose sodium 12 Polyvinylpyrrolidone 6 Magnesium stearate 3 (d) Tablet IV mg/tablet CompoundX 1 Lactose Ph.Eur 92 Croscarmellose sodium 4 Polyvinylpyrrolidone 2 Magnesium stearate 1 Capsule mg/capsule Compound X 10 Lactose Ph.Eur 389 Croscarmellose sodium 100 Magnesium stearate 1 Injection I Compound X 50% w/v Isotonic aqueous solution to 100% Injection H (e.g. bolus) Compound X 10% w/v Isotonic aqueous solution to 100% Injection TIT CompoundX 5% w/v Isotonic aqueous solution to 100% Injection IV (e.g. infusion) Compound X 1% w/v Isotonic aqueous solution to 100% Buffers, pharmaceutically-acceptable surfactants, oils or cosolvents such as polyethylene glycol, polypropylene glycol, glycerol or ethanol, glidants (such as silicon dioxide) or complexing agents such as a cyclodextrin (for example, hydroxypropyl B-cyclodexrrin or sulfobutylether fl-cyclodextrin) may be used to aid formulation. Also, improvements in aqueous solubility, if desired, maybe achieved, for example, by conjugation of a compound of formula (1) with a phospholipid (such as a (phospho)choline derivative) to form a micellar emulsion. Note: The above formulations may be obtained by conventional procedures well known in the pharmaceutical art, for example as described in "Remington: The Science & Practice of Pharmacy" Vols. I & II (Ed. A.R.Gennaro (Chairman) et al; Publisher: Mack Pubhshing Company, Easton, Pennsylvania; 19th Edition -1995) and 'Tharmaceutics - The Science of Dosage Form Design" (Ed. M.E.Aulton; Publisher: Churchill Livingstone; first published 1988). The tablets (a)-(d) may be (polymer) coated by conventional means, for example to provide an enteric coating of cellulose acetate phthalate. 1. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo- hydrolysable ester thereof, ' wherein HET is an N-linked 5-membered heteroaryl ring, containing either (i) 1 to 3 further nitrogen heteroatoms or (ii) a further heteroatom selected from 0 and S together with an optional further nitrogen heteroatom; which ring is optionally substituted onaC atom by an oxo or thioxo group; and/or the ring is optionally substituted on a C atom by 1 or 2 (l-4C)alkyl groups; and/or on an available nitrogen atom (provided that the ring is not thereby quaternised) by (l-4C)a!kyl; or HET is an N-linked 6-membered heteroaryl ring containing up to three nitrogen heteroatoms in total (including the linking heteroatom), which ring is substituted on a suitable C atom by oxo or thioxo and optionally substituted on any available C atom by 1 or 2 (l-4C)alkyl substituents; Q is selected from Ql to Q9 :- wherein R2 and R3 are independently hydrogen or fluoro; wherein A3 is carbon or nitrogen; Bj is O or S (or, in Q9 only, NH); Xq is O, S or N-R1 (wherein R1 is hydrogen, (l-4C)alkyl or hydroxy~(l-4C)alkyl); and wherein in Q7 each Aj is independently selected from carbon or nitrogen, with a maximum of 2 nitrogen heteroatoms in the 6-membered ring, and Q7 is linked to T via any of the At atoms (when A, is carbon), and linked in the 5-membered ring via the specified carbon atom, or via Ax when At is carbon; Q8 is linked to T via either of the specified carbon atoms in the 5- membered ring, and linked in the benzo-ring via either of the two specified carbon atoms on either side of the linking bond shown; and Q9 is linked via either of the two specified carbon atoms on either side of the linking bond shown; wherein T is selected from the groups in (TA) to (TD) below (wherein AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 are defined hereinbelow); (TA) T is selected from the following groups :- (TAa) AR1, ARl-(l-4C)alkyl-, AR2 (carbon linked), AR3; (TAb) ARl-CH(OH), AR2-CH(OH)-, AR3-CH(OH)-; (TAc) ARl-CO-,AR2-CO-9AR3-CO-,AR4-CO-; (TAd) AR1-0-, AR2-0-, AR3-0-; (TAe) AR1-S(0)q-, AR2-S(0)q-, AR3-S(0)q- (qis 0,1 or 2); (TAf) an optionally substituted N-linked (fully unsaturated) 5-membered heteroaryl ring system containing 1,2 or 3 nitrogen atoms; (TAg) a carbon linked tropol-3-one or tropol-4-one, optionally substituted in a position not adjacent to the linking position; or (TB) T is selected from the following groups :- (TBa) haloor(l-4C)alkyl {optionally substituted by one or more groups each independently selected from hydroxy, (1- 4C)alkoxy, (l-4C)alkanoyl, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, -NRvRw, (1- 6C)alkanoylamino, (l-4C)alkoxycarbonylamino, H-(l-4C)alkyl-M-(l-6C)alkanoylarnino, (1- 4C)alkylS(0)q- (q is 0,1 or 2), CY1, CY2 or AR1}; (TBb) -NRv'Rw1; (TBc) ethenyL 2-(l-4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-((l-4Qaltylarnmocarbonyl)ethenyl, 2-((l-4C)alkoxycarbonyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl; (TBd) R10CO-, R10S(O)q- (q is 0,1 or 2) or RI0CS- wherein R10 is selected from the following groups :- (TBda) CYlorCY2; (TBdb) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw, ethenyl, 2-(l- 4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyI, 2-nitro-2- ((l-4C)alkyl)ethenyl, 2-((l-4C)alkylarninocarbonyl)ethenyli 2-((l- 4C)alkoxycarbonyl)ethenyl, 2-(ARl)ethenyl or 2-(AR2)ethenyl; or (TBdc) (l-4C)alkyl {optionally substituted as defined in (TBa) above, or by (1- 4C)alkylS(0)pNH- or (l-4C)alkylS(0)p.((l-4C)alkyl)N- (p is 1 or 2)}; wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl; Rv1 is hydrogen, (1- 4C)alkyl or (3-8C)cycloalkyl; Rw1 is hydrogen, (l-4C)alkyl, (3-8C)cycloallcyl, (l-4C)alkyl- CO- or (l-4C)alkylS(0)q- (q is 1 or 2); or (TQ T is selected from the following groups :- (TCa) an optionally substituted, fully saturated 4-membered monocyclic ring containing 1 heteroatom selected from 0, N and S (optionally oxidised), and linked via a ring nitrogen or sp3 carbon atom; (TCb) an optionally substituted 5-menibered monocyclic ring containing 1 heteroatom selected from 0, N and S (optionally oxidised), and linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom, which monocyclic ring is folly saturated other than (where appropriate) at a linking sp2 carbon atom; (TCc) an optionally substituted 6- or 7-membered monocyclic ring containing 1 or 2 heteroatoms independently selected from O, N and S (optionally oxidised), and linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom, which monocyclic ring is fully saturated other than (where appropriate) at a linking sp2 carbon atom; or (TD) T is selected from the following groups :- (TDa) a bicyciic spiro-ring system containing 0,1 or 2 ring nitrogen atoms as the only ring heteroatoms, the structure consisting of a 5- or 6-membered ring system (linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom) substituted (but not adjacent to the miking position) by a 3-, 4- or 5-membered spko-carbon-linked ring; which bicyciic ring system is (i) fully saturated other than (where appropriate) at a linking sp2 carbon atom; (ii) contains one -N(Rc)- group in the ring system (at least two carbon atoms away from the linking position when the link is via a nitrogen atom or an sp2 carbon atom) or one -N(Rc)- group in an optional substituent (not adjacent to the linking position) and is (hi) optionally further substituted on an available ring carbon atom; or (TDb) a 7-, 8- or 9-membered bicyciic ring system (linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom) containing 0,1 or 2 ring nitrogen atoms (and optionally a further O or S ring heteroatom), the structure containing a bridge of 1,2 or 3 carbon atoms; which bicyciic ring system is (i) fully saturated other than (where appropriate) at a linking sp2 carbon atom; (ii) contains one 0 or S heteroatom, or one -N(Rc)- group in the ring (at least two carbon atoms away from the linking position when the link is via a nitrogen atom or an sp2 carbon atom) or one -N(Rc)- group in an optional substituent (not adjacent to the linking position) and is (in) optionally further substituted on an available ring carbon atom; wherein Re is selected from groups (Rcl) to (Rc5) :- (Rcl) (l-6C)alkyl {optionally substituted by one or more (l-4C)alkanoyl groups (including geminal disubstitution) and/or optionally monosubstituted by cyano, (l-4C)alkoxy, trifluoromethyl, (l-4C)alkoxycarbonyl, phenyl (optionally substituted as for AR defined hereinafter), (l-4C)alkylS(0)q- (q is 0,1 or 2); or, on any but the first carbon atom of the (1-6C)alJkyl chain, optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy and fluoro, and/or optionally monosubstituted by oxo, -NRvRw [wherein Rv is hydrogen or (l-4C)a!kyl; Rw is hydrogen or (l-4C)alkyl], (l-6C)alkanoylamino, (l-4C)alkoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylamino, (l-4C)alkylS(0)pNH- or (l-4C)alkylS(0)p.((l-4C)alkyl)N- (p is 1 or 2)}; (Rc2) R13CO-,R13S02-orR13CS- wherein R13 is selected from (Rc2a) to (Rc2e) :- (Rc2a) AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1, CY2; (Rc2b) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], ethenyl, 2-(l-4C)alkylethenyl, 2- cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-((l-4C)alkylaminocarbonyl)ethenyl, 2-((l-4C)alkoxycarbonyl)ethenyl3 2-(ARl)ethenyl, 2-(AR2)ethenyl, 2-(AR2a)ethenyl; (Rc2c) (l-10C)alkyl {optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy, (1-10C)alkoxy, (l-4C)alkoxy-(l-4C)alkoxy, (1- 4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxy, (l-4C)alkanoyl, phosphoryl [-0-P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphiryl [-0-P(OH)2 and mono- and di-(l- 4C)alkoxy derivatives thereof], and amino; and/or optionally substituted by one group selected from phosphonate [phosphono, -P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphinate [-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives thereof], cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l- 4C)alkoxycarbonyi, (l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxycarbonyL (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-6C)alkanoylamino, (l-4C)a]koxycarbonylamino, N-(l-4C)alkyl-N- (l-6C)alkanoylamino, (l-4QalkylaminocarbonylJ di((l-4C)alkyl)aminocarbonyl, (1- 4C)altylS(0)prra-,(l-4C)altylS(0)p-((l-4C)^^ fluoro(l-4C)alkylS(0)p((14C)alkyl)N-, (l-4C)alkylS(0)q- [the (l-4C)alkyl group of (1-4C)aJkylS(0)q- being optionally substituted by one substituent selected from hydroxy, (1 -4C)alkoxy, (1 -4C)alkanoyl, phosphoryl [-O-P(0)(OH)2, and mono- and di-(l -4C)alkoxy ■ derivatives thereof], phospbiryl [-0-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives thereof], amino, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxycarbonyl, carboxy, (1-4C)alkylamino, di((l-4C)alkyl)arnino, (l-6C)alkanoylamino, (l-4C)aUcoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylairnno, (l-4C)alkylaminocarbonyl, di((l-4C)alkyl)aminocarbonyl, (l-4C)alkylS(0)pNH-, (l-4C)aU (Rc2d) R14C(0)O(l-6C)aftyI wherein R14is AR1, AR2, (l-4C)aUcylamino (the (1- 4Qalkyl group being optionally substituted by (l-4C)alkoxycarbonyl or by carboxy), benzyloxy-(l-4C)alkyl or (l-10C)alkyl {optionally substituted as defined for (Rc2c)}; (Rc2e) R150- wherein R,s is benzyl, (l-6C)allcyl {optionally substituted as defined for (Rc2c)}, CY1, CY2 or AR2b; (Rc3) hydrogen, cyano, 2-cyanoethenyl, 2-cyano-2-((l-4C)allcyi)ethenyl, 2-((l-4C)alkylaminocarbonyl)ethenyl, 2-((l-4C)alkoxycarbonyl)ethenyl, 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl, or of me formula (Rc3a) wherein X00 is -OR17, -SR17, -NHR17and -N(R17)2; wherein R17 is hydrogen (when X00 is -NHRI7and -NfR17)^, and R17 is (l-4C)alkyl, phenyl or AR2 (when X00 is -OR17, -SR17 and -NHR17); and R16 is cyano, nitro, (l-4C)alkylsulfonyl, (4-7C)cycloalkylsulfonyl, phenylsulfonyl, (l-4C)ali:anoyl and (l-4C)alkoxycarbonyl; (Rc4) trityl, AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b; (RcS) RdOC(Re)=CH(C=0)-, RfC(=0)C(=0)-, RgN=C(Rh)C(=0)-or RiNHC(Rj)=CHC(=0)- wherein Rd is (l-6C)alkyl; Re is hydrogen or (l-6C)alkyl, or Rd and Re together form a (3-4C)alkylene chain; Rf is hydrogen, (l-6C)alkyL hydroxy(l-6C)alkyl, (l-6C)alkoxy(l-6C)alkyl, -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], (l-6C)a!koxy, (l-6C)alkoxy(l-6C)alkoxy, hydroxy(2-6C)alkoxy, (1- 4C)alkylamino(2-6C)alkoxy, di-(l-4C)alkylamino(2-6C)alkoxy; Rg is (l-6C)alkyl, hydroxy or (l-6C)alkoxy; Rh is hydrogen or (l-6C)alkyl; Ri is hydrogen, (l~6C)alkyl, AR1, AR2, AR2a, AR2b and Rj is hydrogen or (1 -6C)alkyl; wherein AR1 is an optionally substituted phenyl or optionally substituted naphtbyl; AR2 is an optionally substituted 5- or 6-membered, fully unsaturated (i.e with the maximum degree of unsaturation) monocyclic heteroaryl ring containing up to four heteroatoms independently selected from O, N and S (but not containing any O-O, O-S or S-S bonds), and linked via a ring carbon atom, or a ring nitrogen atom if the ring is not thereby quaternised; AR2a is a partially hydrogenated version of AR2 (i.e. AR2 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom or linked via a ring nitrogen atom if the ring is not thereby quaternised; AR2b is a fully hydrogenated version of AR2 (i.e. AR2 systems having no unsaturation), linked via a ring carbon atom or linked via a ring nitrogen atom; AR3 is an optionally substituted 8-, 9- or 10-membered, fully unsaturated (i.e with the maximum degree of unsaturation) bicyclic heteroaryl ring containing up to four heteroatoms independently selected from 0, N and S (but not containing any 0-0, O-S or S-S bonds), and linked via a ring carbon atom in either of the rings comprising the bicyclic system; AR3a is a partially hydrogenated version of AR3 (i.e. AR3 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom if the ring is not thereby quaternised, in either of the rings comprising the bicyclic system; AR3b is a fully hydrogenated version of AR3 (i.e. AR3 systems having no unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom, in either of the rings comprising the bicyclic system; AR4 is an optionally substituted 13- or 14-membered, fully unsaturated (i.e with the maximum degree of unsaturation) tricyclic heteroaryl ring containing up to four heteroatoms independently selected from O, N and S (but not containing any O-O, 0-S or S-S bonds), and linked via a ring carbon atom in any of the rings comprising the tricyclic system; CY2 is an optionally substituted cyclopentenyl or cyclohexenyl ring. ■ 2. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, ^ claimed in claim 1; wherein Q is Ql wherein R2 md R3 arQ independently hydrogen or fluoro; ^6. the groups defined in (TCa) to (TCc) are defined by formulae (TCI) to (TC4) :- wherein in (TCI) : >A3-B3- is >C(Rq)~CH(Rr)- and G is -0-, -S-, -SO-, -S02- or >N(Rc); wherein in (TC2) : ml is 0,1 or 2; >A3-B3- is >C=C(Rr)- or >C(Rq)-CH(Rr)- and G is -0-, - !-,-SO-,-S02-or>N(Rc); therein in (TC3): ml is 0,1 or 2; >A3-B3- is >C(Rq)-CH(Rr)- (other than when Rq and Rr re both together hydrogen) and G is -0-, -S-, -SO-, -S02- or >N(Rc); /herein in (TC4) : nl is 1 or 2; ol is 1 or 2 and nl + ol = 2 or 3; >A3-B3- is >C=C(Rr)- or -C(Rq)-CH(Rr)- or >N-CH2- and G is -0-, -S-; -SO-, -S02- or >N(Rc); Rp is hydrogen, (1-4C)alkyl (other than when such substitution is defined by >A3-B3-), hydroxy, (l-4C)allcoxy or (l-4C)alkanoyloxy; wherein in (TCI), (TC2) and (TC4); ml, nl and ol are as defined hereinbefore: >A3-B3- is >N-CH2- and G is >C(RU)(R12), >C=0, >C-OH, >C-(l-4C)alkoxy, >C=N-OH, >C=N-(l-4C)alkoxy, X>N-NH-(l-4C)alkyl, >C=N-N((l-4C)alkyl)2 (the last two (1- 4C)alkyl groups above in G being optionally substituted by hydroxy) or >C=N-N-CO-(l- 4C)alkoxy; wherein > represents two single bonds; Rq is hydrogen, hydroxy, halo, (l -4C)alkyl or (1 -4C)alkanoyloxy; Rr is (independently where appropriate) hydrogen or (l-4C)alkyl; Ru is hydrogen, (l-4C)alkyl, fluoro(l-4C)alkyl, (l-4C)alkyl-thio-(l-4C)alkyl orhydroxy-(l- 4C)alkyl and R12 is -[C(Rr)(Rr)]^-N(Rr)(Rc) wherein m2 is 0,1 or 2; and, other than the ring substitution defined by G, >A3-B3- and Rp, each ring system may be optionally further substituted on a carbon atom not adjacent to the link at >A3- by up to two substituents independently selected from (l-4C)alkyl, fluoro(l-4C)alkyl (including trifluoromethyl), (l-4C)alkyl-thio-(l-4C)alkyl, hydroxy-(l-4C)alkyl, amino, arnino-(l- 4C)aIkyl, (l-4C)alkanoylamino, (l-4C)alkanoylamino-(l-4C)alkyl, carboxy, (1- 4C)alkoxycarbonyl, AR-oxymethyl, AR-thiomethyl, oxo (=0) (other than when G is >N-Rc and Re is group (Rc2) defined hereinbefore) or independently selected from Re; and also hydroxy or halo (the last two optional substituents only when G is -0- or -S-); wherein AR is optionally substituted phenyl, optionally substituted phenyl(l-4C)alkyl, optionally substituted naphthyl, optionally substituted 5- or 6-membered heteroaryl; an optionally substituted 5/6 or 6/6 bicyclic heteroaryl ring system, in which the bicyclic heteroaryl ring systems may be linked via an atom in either of the rings comprising the bicyclic system, and wherein both the mono- and bicyclic heteroaryl ring systems are linked via a ring carbon atom and may be (partially) hydrogenated; and Re is selected from groups (Rcl) to (Rc5) defined in claim 1. 3. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, as claimed in claims 1 and 2, in which the optional substituents in AR are independently selected from halo, (l-4C)alkyl, hydroxy, nitro, carbamoyl, (1-4Cfzlkylc£rtttinoyI, di-({l-4C}a&y{)carbamoyl, cyaao, trifluoromethyl, triftuorametboxy, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-4C)alkyl S(O) - (q is 0,1 or 2), carboxy, (l-4C)alkoxycarbonyl, (2-4C)atbnyl, (2-4C)alkynyl, (l-4C)alkanoyl, (l-4C)alkoxy, (1-4C)alkylS(0) 2amino, (l-4C)alkanoylamino, benzoylamino, benzoyl, phenyl (optionally substituted by up to three substituents selected from halo, (l-4C)alkoxy or cyano), furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene, hydroxyimino (l-4C)alkyl, (l-4C)alkoxyimino(l-4C)alkyl, hydroxy-(l- 4C)alkyl, halo-(l-4C)alkyl, nitro(l-4C)alkyl, amino(l-4C)alkyl, cyano(l- 4C)alkyl, (l-4C)alkanesulfonamido, aminosulfonyl, (1- 4C)alkylaminosulfonyl and di-((l-4C)alkyl)aminosulfonyl. 4. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, as claimed in any of claims 1 to 3, wherein the groups defined in (TCa) to (TCc), and (TCI) to (TC4) are defined by formulae (TC5) to (TC11) :- wherein Re is as defined in claim 1. 5. A compound of the formula (IC), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, as claimed in any of claims 1 to wherein HET is as claimed in any of claims 1 to 4; R2 and R3 are independently hydrogen or_fluoro; Rpl and Rp2 are independently hydrogen, AR-oxymethyl or AR-thiomethyl [wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene], (l-4C)alkyl, carboxy, (1-4C)alkoxycarbonyl, hydroxymethyl, (l-4C)aIkoxymethyl or carbamoyl and Rep is cyano, pyrimidin- 2-yl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl or Rep is of the formula R10PCO-, R10PSO2- or RIOPCS-{wherein R10P is hydrogen, (l-5C)alkyl [optionally substituted by one or more groups each independently selected from hydroxy and amino, or optionally monosubstituted by [l-4C]alkoxy, (l-4C)alkylS(0)q-, (1-4C)alkylamino, (l-4C)alkanoyl, naphthoxy, (2-6C)alkanoylamino or (1-4C)alkylS(0)pNH- wherein p is 1 or 2 and q is 0, 1 or 2], imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, pyridoimidazole, pyrimidoimidazole, quinoxaline, quinazoline, phthalazine, cinnoline or naphthyridine, or R10P is of the formula RHP C(0)0(l-6C)alkyl wherein RUP is (l-6C)alkyI}, or Rep is of the formula RfC(=0)C(=0)- wherein Rf is (l-6C)alkoxy. 6. A compound of the formula (IC), or a pharmaceutically-acceptable salt, or an in-uifo-hydrolysable ester thereof, as claimed in any of claims 1 to 5, wherein HET is triazole or tetrazole. 7. A compound, as claimed in any of claims 1 to 6, being ((5R)-3-(4-(l -(2-Hydroxyacetyl)-1,2,5,6-tetrahydropyridin-4-yl)-3,5-difluorophenyl) -5- (1,2,3-traizol-1 -ylmethyl) oxazolidin-2-one; ((5R)-3-(4-(l-(2S)-2,3-Dihydroxypropionyl)-l,2,5,6-tetrahydropyridin-4-yl)-3,5-difluoro phenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazolidin-2-one; (5R)-3-(4-( 1 -(2-Hydroxyacetyl)-1,2,5,6-te1xahydropyridin-4-yl)-3-fluorophenyl)-5-(l ,2,3-triazol-l-ylmethyl)oxazolidin- 2-one; (5R)-3-(4-(l-(2S)-2,3-Dihydroxypropionyl)-l,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)- 5-(l,2,3-triazol-l-ylmethyl)oxazolidin-2-one; or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof. 8. A compound, as claimed in claim 1, being (5R)-3-(3,5-Difluoro-4-(3,6-dihydro-l,l-dioxo-2H-thiopyran-4-yl)phenyl)-5-( 1,2,3-triazol-1 -ylmethyl)oxazolidin-2-one. 9. A process for the preparation of a compound of the formula (I) as claimed in claim 1, or pharmaceutically-acceptable salts or in vivo hydrolysable esters thereof, which comprises of (a) to (d) :- (a) modification of a substituent in or introduction of a substituent into another compound of formula (I);. (b) reaction of a compound of formula (II) : III wherein Y is a displaceable group (which may be preformed such as chloro or mesylate, or generated in-situ, for example under Mitsunobu conditions) with a compound of the formula (III) : HET (III) wherein HET is HET -H free-base form or HET -anion formed from the free base form; or (c) reaction of a compound of the formula (IV) : (IV) wherein Z is an isocyanate, amine or urethane group with an epoxide of the formula (V) : (V) (d) for HET as 1,2,3-triazole cycloaddition via the azide (wherein Y in (II) is azide); and thereafter if necessary: (i) removing any protecting groups; (ii) forming a pharmaceutically-acceptable salt; (iii) forming an in-vivo hydrolysable ester. 10. A pharmaceutical composition which comprises a compound of the formula [I] as claimed in any one of claims 1 to 8, or a pharmaceutically- acceptable salt or an in-vivo hydrolysable ester thereof, and a pharmaceutically-acceptable diluent or carrier. Dated this Ist day of October, 2002. [ JAYANTA PAL] OF REMRRY &SAGAR ATTORNEY FOR THE APPLICANTS

Full Text

FORM 2
THE PATENTS ACT 1970
[39 OF 1970]
COMPLETE SPECIFICATION
[See Section 10, Rule 13]
"OXAZOLIDINONE DERIVATIVES WITH ANTIBIOTIC ACTIVITY"
ASTRAZENECA AB, a Swedish company of S-151 85 Sodertalje, Sweden,

The following specification particularly describes the nature of the invention and the manner in which it is to be performed:-

The present invention relates to antibiotic compounds and in particular to antibiotic compounds containing a substituted oxazolidmone ring. This invention further relates to processes for their preparation, to intermediates useful in their preparation, to their use as therapeutic agents and to pharmaceutical compositions containing them.
The international microbiological community continues to express serious concern that the evolution of antibiotic resistance could result in strains against which currently available antibacterial agents will be ineffective. In general, bacterial pathogens may be classified as either Gram-positive or Gram-negative pathogens. Antibiotic compounds with effective activity against both Gram-positive and Gram-negative pathogens are generally regarded as having a broad spectrum of activity. The compounds of the present invention are regarded primarily as effective against Gram-positive pathogens because of their particularly good activity against such pathogens, but are also regarded as effective against certain Gram-negative pathogens.
Gram-positive pathogens, for example Staphylococci, Enterococci, Streptococci and mycobacteria, are particularly important because of the development of resistant strains which are both difficult to treat and difficult to eradicate from the hospital environment once established. Examples of such strains are methicillin resistant staphylococcus (MRS A), methicillin resistant coagulase negative staphylococci (MRCNS), penicillin resistant Streptococcus pneumoniae and multiply resistant Enterococcus faecium.
The major clinically effective antibiotic for treatment of such resistant Gram-positive pathogens is vancomycin. Vancomycin is a glycopeptide and is associated with nephrotoxicity and ototoxicity. Furthermore, and most importantly, antibacterial resistance to vancomycin and other glycopeptides is also appearing. This resistance is increasing at a steady rate rendering these agents less and less effective in the treatment of Gram-positive pathogens. There is also now increasing resistance appearing towards agents such as p -lactams, quinolones and macrolides used for the treatment of certain Gram negative strains responsible for upper respiratory tract infections. These strains include H.influenzae and M.catarrhalis.
Certain antibacterial compounds containing an oxazolidinone ring have been described

in the art (for example, Walter A. Gregory et al in J.Med.Chem. 1990, 33,2569-2578 and 1989, 32(8), 1673-81; Chung-Ho Park et al in J.Med.Chem. 1992, 35, 1156-1165). Such antibacterial oxazolidinone compounds with a 5-methylacetamide sidechain may be subject to mammalian peptidase metabolism. Furthermore, bacterial resistance to known antibacterial agents may develop, for example, by (i) the evolution of active binding sites in the bacteria rendering a previously active pharmacophore less effective or redundant, and/or (ii) the evolution of means to chemically deactivate a given pharmacophore. Therefore, there remains an ongoing need to find new antibacterial agents with a favourable pharmacological profile, in particular for compounds containing new pharmacophores.
We have discovered a class of antibiotic compounds containing a new class of substituted oxazolidinone ring which has useful activity against Gram-positive pathogens including MRSA and MR.CNS and, in particular, against various strains exhibiting resistance to vancomycin and against E. faecium strains resistant to both aminoglycosides and clinically used pMactams, but also to fastidious Gram negative strains such as H.influenzae and Mxatarrhalis.
Accordingly the present invention provides a compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof,

wherein
HET is an N-linked 5-membered heteroaiyl ring, containing either (i) 1 to 3 further nitrogen heteroatoms or (ii) a further heteroatom selected from O and S together with an optional further nitrogen heteroatom; which ring is optionally substituted on a C atom by an oxo or thioxo group; and/or the ring is optionally substituted on a C atom by 1 or 2 (l-4C)alkyl groups; and/or on an available nitrogen atom (provided that the ring is not thereby quaternised) by (l-4C)aIkyl; or

HET is an N-linked 6-membered heteroaryl ring containing up to three nitrogen heteroatoms in total (including the linking heteroatom), which ring is substituted on a suitable C atom by oxo or thioxo and optionally substituted on any available C atom by 1 or 2 (l-4C)alkyl substituents;
Q is selected from Ql to Q9 :-

wherein R2 and R3 are independently hydrogen or fluoro;
wherein A1 is carbon or nitrogen; B1 is 0 or S (or, in Q9 only, NH); Xq is 0, S or N-R1
(wherein R1 is hydrogen, (l-4C)alkyl or hydroxy-(l-4C)alkyl); and wherein
in Q7 each A1 is independently selected from carbon or nitrogen, with amaxirnum of 2

nitrogen heteroatoms in the 6-membered ring, and Q7 is linked to T via any of the A1 atoms
(when A1 is carbon), and linked in the 5-membered ring via the specified carbon atom, or via
Al when A, is carbon; Q8 is linked to T via either of the specified carbon atoms in the 5-
membered ring, and linked in the benzo-ring via either of the two specified carbon atoms on
either side of the linking bond shown; and Q9 is linked via either of the two specified carbon
atoms on either side of the linking bond shown;
wherein T is selected from the groups in (TA) to (TD) below (wherein AR1, AR2, AR2a,
AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 are defined hereinbelow);
(TA) T is selected from the following groups :-
(TAa) AR1, ARl-(l-4C)alkyl-, AR2 (carbon linked), AR3;
(TAb) ARl-CH(OH),AR2-CH(OH)-,AR3-CH(OH)s
(TAc) AR1 -CO-, AR2-CO-, AR3-CO-, AR4-CO-;
(TAd) AR1-0-, AR2-0-, AR3-0-;
(TAe) AR1-S(0)q-, AR2-S(0)q-, AR3-S(0)q- (q is 0,1 or 2);
(TAf) an optionally substituted N-linked (fully unsaturated) 5-membered heteroaryl ring
system containing 1,2 or 3 nitrogen atoms;
(TAg) a carbon linked tropol-3-one or tropol-4-one, optionally substituted in a position not
adjacent to the linking position; or
(TB) T is selected from the following groups :-
(TBa) halo or (l-4C)alkyl
{optionally substituted by one or more groups each independently selected from hydroxy, (1-
4C)alkoxy, (l-4C)alkanoyl, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, -NRvRw, (1-
6C)alkanoylamino, (l-4C)alkoxycarbonylamino, N-(l-4C)aIkyl-N-(l-6C)aUcanoylarnino, (1-
4C)alkylS(0)q- (q is 0,1 or 2), CY1, CY2 or AR1};
(TBb) -NRv'Rw1;
(TBc) ethenyl, 2-(l-4C)alkylethenyL 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-
nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-((l-4C)alkylarninocarbonyl)ethenyl, 2-((l-
4C)allcoxycarbonyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl;
(TBd) R10CO-, R10S(O)q- (q is 0,1 or 2) or RI0CS-
wherein R10 is selected from the following groups :-

(TBda) CYl or CY2;
(TBdb) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw, ethenyl, 2-(l-
4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyl, 2-nitro-2-
((l-4C)alkyl)ethenyl, 2-((l-4C)alkylammocarbonyl)ethenyl, 2-((l-
4C)alkoxycarbonyl)etlienyl) 2-(ARl)ethenyl or 2-(AR2)ethenyl; or
(TBdc) (l-4C)alkyl {optionally substituted as defined in (TBa) above, or by (1-
4C)alkylS(0)pNH- or (l-4C)alkylS(0)p.((l-4C)alkyl)N- (p is 1 or 2)};
wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl; Rv' is hydrogen, (1-
4C)alkyl or (3-8C)cycloalkyl; Rw1 is hydrogen, (l-4C)alkyi, (3-8C)cycloalkyl, (l-4C)alkyl-
CO-or (l-4C)alkylS(0)q-(q is 1 or 2); or
(TC) T is selected from the following groups :-
(TCa) an optionally substituted, fully saturated 4-membered monocyclic ring containing 1
heteroatom selected from O, N and S (optionally oxidised), and linked via a ring nitrogen or
sp3 carbon atom;
(TCb) an optionally substituted 5-membered monocyclic ring containing 1 heteroatom
selected from O, N and S (optionally oxidised), and linked via a ring nitrogen atom or a ring
sp3 or sp2 carbon atom, which monocyclic ring is fully saturated other than (where
appropriate) at a linking sp2 carbon atom;
(TCc) an optionally substituted 6- or 7-membered monocyclic ring containing 1 or 2
heteroatoms independently selected from O, N and S (optionally oxidised), and linked via a
ring nitrogen atom or a ring sp3 or sp2 carbon atom, which monocyclic ring is fully saturated
other than (where appropriate) at a linking sp2 carbon atom; or
(TD) T is selected from the following groups :-
(TDa) a bicyclic spiro-ring system containing 0,1 or 2 ring nitrogen atoms as the only ring
heteroatoms, the structure consisting of a 5- or 6-membered ring system (linked via a ring
mtrogen atom or a ring sp3 or sp2 carbon atom) substituted (but not adjacent to the linking
position) by a 3-, 4- or 5-membered spiro-carbon-linked ring; which bicyclic ring system is
(i) fully saturated other than (where appropriate) at a linking sp2 carbon atom;
(ii) contains one -N(Rc)- group in the ring system (at least two carbon atoms away from

the linking position when the link is via a nitrogen atom or an sp2 carbon atom) or one -N(Rc)-
group in an optional substituent (not adjacent to the linking position) and is
(iii) optionally further substituted on an available ring carbon atom; or
(TDb) a 7-, 8- or 9-membered bicyclic ring system (linked via a ring nitrogen atom or a ring
sp3 or sp2 carbon atom) containing 0,1 or 2 ring nitrogen atoms (and optionally a further 0 or
S ring heteroatom), the structure containing a bridge of 1, 2 or 3 carbon atoms; which bicyclic
ring system is
(i) fully saturated other than (where appropriate) at a linking sp2 carbon atom;
(ii) contains one O or S heteroatom, or one -N(Rc)- group in the ring (at least two carbon
atoms away from the linking position when the link is via a nitrogen atom or an sp2 carbon
atom) or one -N(Rc)- group in an. optional substituent (not adjacent to the linking position)
and is
(iii) optionally further substituted on an available ring carbon atom;
wherein Re is selected from groups (Rcl) to (Rc5) :-
(Rcl) (l-6C)alkyl {optionally substituted by one or more (l-4C)alkanoyl groups (including geminal disubstitution) and/or optionally monosubstituted by cyano, (l-4C)alkoxy, trifluoromethyl, (l-4C)alkoxycarbonyl, phenyl (optionally substituted as for AR defined hereinafter), (l-4C)alkylS(0)q- (q is 0,1 or 2); or, on any but the first carbon atom of the (1-6C)alkyl chain, optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy and fluoro, and/or optionally monosubstituted by oxo, -NRvRfy [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], (l-6C)alkanoylamino, (l-4C)antoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylamino, (l-4C)aIkylS(0)pNH- or (l-4C)alkylS(0)p-((l-4C)alkyl)N- (p is 1 or 2)}; (Rc2) R13CO- , R13S02- or Rl3CS-wherein R13 is selected from (Rc2a) to (Rc2e) :-
(Rc2a) AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1, CY2;
(Rc2b) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw [wherein Rv is
hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], ethenyl, 2-(l-4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)aJJcyi)ethenyl, 2-nitroethenyL 2-nitro-2-((l-4C)alkyI)ethenyL
2-((l-4C)alkylaminocarbonyl)ethenyl

2-((l-4C)alkoxycarbonyl)ethenyI, 2-(ARl)ethenyl, 2-(AR2)ethenyl, 2-(AR2a)ethenyl;
(Rc2c) (l-lOC)alkyl
{optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy, (l-lOC)alkoxy, (l-4C)alkoxy-(l-4C)alkoxy, (1-4C)aIkoxy-(l-4C)aIkoxy-(l-4C)alkoxy, (l-4C)aIkanoyl,phosphoryl [-0-P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphiryl [-0-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives thereof], and amino; and/or optionally substituted by one group selected from phosphonate [phosphono, -P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphinate [-P(OH), and mono- and di-(l-4C)alkoxy derivatives thereofj, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)aIkoxycarbonyl, (1 -4C)alkoxy-(l -4C)allcoxy-(l -4C)alkoxycarbonyl, (1 -4C)aUcylarnino, di((l-4C)all£yl)amino, (l-6C)aUcanoylamino, (l-4C)alkoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylamino, (l-4C)alkylaminocarbonyl, di((l-4C)alkyl)aminocarbonyl, (1-4C)alkylS(0)pNH-, (l-4C)alkylS(0)p-((l-4C)alkyl)N-, fluoro(l-4C)allcylS(0)pNH-, fluoro(l-4C)alkylS(0)p((l-4C)allcyl)N-, (l-4C)alkylS(0)q- [the (l-4C)alkyl group of (1-4C)alkylS(0)q- being optionally substituted by one substituent selected from hydroxy, (1-4C)alkoxy, (l-4C)allcanoyl, phosphoryl [-0-P(0)(OH)2, and mono- and di-(l-4C)alkoxy derivatives thereof], phosphiryl [-0-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives thereofj, amino, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxycarbonyl, carboxy, (1-4C)altylamino, di((l^C)alkyl)amino, (l-6C)alkanoylamino, (l-4C)alkoxycarbonylarnino, N-(l-4C)aUcyl-N-(l-6C)aIkanoylamino, (l-4C)alkylaminocarbonyl} di((l-4C)alkyl)aminocarbonyl, (l-4C)alkylS(0)pNH-, (l-4C)alkylS(0)p-((l-4C)alkyl)N-, (1-4C)alkylS(0)q-, AR1-S(0)q-, AR2-S(0)q-, AR3^S(0)q- and also AR2a, AR2b, AR3a and AR3b versions of AR2 and AR3 containing groups], CY1, CY2, AR1, AR2, AR3, AR1-0-, AR2-0-, AR3-0-, AR1-S(0)q-, AR2-S(0)q-, AR3-S(0)q-, AR1-NH-, AR2-NH-, AR3-NH-(p is 1 or 2 and q is 0,1 or 2), and also AR2a, AR2b, AR3a and APv3b versions of AR2 and AR3 containing groups};
(Rc2d) R14C(0)0(l-6C)alkyl wherein R14is AR1, AR2, (l-4C)alkylamino (the (1-
4C)alkyl group being optionally substituted by (l-4C)alkoxycarbonyl or by carboxy), benzyloxy-(l-4C)alkyl or (l-10C)alkyl {optionally substituted as defined for (Rc2c)};

(Rc2e) R150- wherein R15 is benzyl, (l-6C)alkyl {optionally substituted as defined for (Rc2c)}5 CY1, CY2 or AR2b;
(Rc3) hydrogen, cyano, 2-cyanoelhenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-((l-4C)all^laminocarbonyl)ethenyl, 2-((l-4C)alkoxycarbonyl)ethenyL 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl, or of the formula (Rc3a)

(Rc3a)
wherein X00 is -OR17, -SR17, -NHR17and -N(R17)2; i wherein R17 is hydrogen (when X00 is -NHR,7and -N(R17)2), and R17 is (l-4C)alkyl, phenyl or AR2 (when X00 is -OR17, -SR17 and -NHR17); and R,e is cyano, nitro, (l-4C)alkylsulfonyl, (4-7C)cycloalkylsulfonyl, phenylsulfonyl, (l-4C)alkanoyl and (l-4C)alkoxycarbonyl; (Rc4) trityl,ARl,AR2,AR2a,AR2b,AR3,AR3a,AR3b; (Rc5) RdOC(Re)=CH(C=0)-, RfC(O)C(=0)-, RgN=C(Rh)C(=0)- or RiNHC(Rj)=CHC(=0)- wherein Rd is (l-6C)alkyl; Re is hydrogen or (l-6C)alkyl, or Rd and Re together form a (3-4C)alkylene chain; Rf is hydrogen, (l-6C)alkyl, hydroxy(l-6C)alkyl, (l-6C)alkoxy(l-6C)alkyl, -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], (l-6C)alkoxy, (l-6C)allcoxy(l-6C)alkoxy, hydroxy(2-6C)allcoxy, (1-4C)aUcylamino(2-6C)alkoxy1 di-(l-4C)a!kylammo(2-6C)an!:oxy; Rg is (l-6C)alkyl, hydroxy or (l-6C)aUcoxy; Rh is hydrogen or (l-6C)alkyl; Ri is hydrogen, (l-6C)alkyl, AR1, AR2, AR2a, AR2b and Rj is hydrogen or (l-6C)alkyl; wherein
AR1 is an optionally substituted phenyl or optionally substituted naphthyl; AR2 is an optionally substituted 5- or 6-membered, fully unsaturated (i.e with the maximum degree of unsaturation) monocyclic heteroaryl ring containing up to four heteroatoms independently selected from O, N and S (but not containing any O-O, 0-S or S-S bonds), and linked via a ring carbon atom, or a ring nitrogen atom if the ring is not thereby quaternised; AR2a is a partially hydrogenated version of AR2 (i.e. AR2 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom or linked via a ring nitrogen

itom if the ring is not thereby quatemised;
AR2b is a fully hydrogenated version of AR2 (i.e. AR2 systems having no unsaturation), linked via a ring carbon atom or linked via a ring nitrogen atom; AB3 is an optionally substituted 8-, 9- or 10-membered, fully unsaturated (i.e with the maximum degree of unsaturation) bicyclic heteroaryl ring containing up to four heteroatoms independently selected from O, N and S (but not containing any O-O, 0-S or S-S bonds), and linked via a ring carbon atom in either of the rings comprising the bicyclic system; AR3a is a partially hydrogenated version of AR3 (i.e. AR3 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom if the ring is not thereby quatemised, in either of the rings comprising the bicyclic system;
AR3b is a rally hydrogenated version of AR3 (i.e. AR3 systems having no unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom, in either of the rings comprising the bicyclic system;
AR4 is an optionally substituted 13- or 14-membered, fully unsaturated (i.e with the maximum degree of unsaturation) tricyclic heteroaryl ring containing up to four heteroatoms independently selected from 0, N and S (but not containing any 0-0, 0-S or S-S bonds), and linked via a ring carbon atom in any of the rings comprising the tricyclic system; AR4a is a partially hydrogenated version of AR4 (i.e. AR4 systems retaining some, but not the full, degree of unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen atom if the ring is not thereby quatemised, in any of the rings comprising the tricyclic system; CY1 is an optionally substituted cyclobutyl, cyclopentyl or cyclohexyl ring; CY2 is an optionally substituted cyclopentenyl or cyclohexenyl ring.
In this specification, where it is stated that a ring may be linked via an sp2 carbon atom, which ring is fully saturated other than (where appropriate) at a linking sp2 carbon atom, it is to be understood that the ring is linked via one of the carbon atoms in a C=C double bond.
In another embodiment, (Rcl) is as defined above other than the optional phenyl substituent on (l-6C)alkyl is optionally substituted as for AR1 defined hereinafter; and (Rc2c), is as defined above and further includes carboxy as an optional substituent on R13 as (l-lOC)alkyl.

(TAf) When T is an optionally substituted N-linked (fully unsaturated) 5-membered heteroaryl ring system containing 1,2 or 3 nitrogen atoms, it is preferably selected from a group of formula (TAfl) to (TAf6) below (particularly (TAfl), (TA£2), (TAf4) and (TAf5), and especially (TAfl) and/or (TA£2)). The above preferred values of (TAf) are particularly preferred when present in Ql or Q2, especially Ql.

(TAf4) (TAfS) (TAf6)
wherein:
R6 is selected (independently where appropriate) from hydrogen, (l-4C)alkyl, (1-
4C)alkoxycarbonyl, (l-4C)alkanoyl, carbamoyl and cyano;
R4 and R5 are independently selected from hydrogen, halo, trifluoromethyl, cyano, nitro, (1-
4C)alkoxy, (l-4C)alkylS(0)q- (q is 0,1 or 2), (l-4C)alkanoyl, (l-4C)alkoxycarbonyl, (2-
4C)alkanoyloxy-(l-4C)alkyL benzoxy-(l-4C)alkyl, (2-4C)allcanoylamino, -CONRvRw, -
NRvRw and (l-4C)alkyl {optionally substituted by hydroxy, trifluoromethyl, cyano, nitro, (1-
4C)alkoxy, (l-4C)alkylS(0)q- (qis 0,1 or 2), (l-4C)allcoxycarbonyl, (MC)alkanoylamino;
-CONRvRw, -NRvRw; wherein RvRw is hydrogen or (l-4C)aIkyl; Rw is hydrogen or (1-
4C)alkyl};

or R4 is selected from one of the groups in (TAfa) to (TAfc) below, or (where appropriate) one of R4 and R5 is selected from the above list of R4 and R5 values, and the other is selected from one of the groups in (TAfa) to (TAfc) below :-(TAfa) a group of the formula (TAfal)

wherein Z° is hydrogen or (l-4C)alkyl;
X° and Y° are independently selected from hydrogen, (l-4C)alkyl, (l-4C)alkoxycarbonyl,
halo, cyano, nitro, (l-4C)alkylS(0)q- (q is 0,1 or 2), RvRwNS02-, trifluoromethyl,
pentafluoroethyl, (l-4C)alkanoyl and -CONRvRw [wherein Rv is hydrogen or (l-4C)alkyl;
Rw is hydrogen or (l-4C)alkyl]; or
one of X° and Y° is selected from the above list of X° and Y° values, and the other is
selected from phenyl, phenylcarbonyL, -S(0)q-phenyl (q is 0,1 or 2), H-
(phenyl)carbamoyl, phenylaminosulfonyl, AR2, (AR2)-CO-, (AR2)-S(0)q- (q is 0,1 or 2),
N-(AR2)carbamoyl and (AR2)aminosulfonyl; wherein any phenyl group in (TAfa) may be
optionally substituted by up to three substituents independently selected from (l-4C)alkyl,
cyano, trifluoromethyl, nitro, halo and (l-4C)alkylsulfonyl;
(TAfb) an acetylene of the formula -=-H or -=-(l-4C)alkyl;
(TAfc) -X1-Y,-AR2, -X'-Y'-ARZa, -X'-Y,-AR2b, -X'-Y'-ARS, -X'-Y'-ARSa or -X'-Y1-
AR3b;
wherein X1 is a direct bond or -CH(OH)- and
Y1 is -(CH^-, -(CH2)n-NH-(CH2)m-, -C0-(CH2)m-, -CONH-(CH2)m-, -C(=S)NH-(CH2)m- or -
C(O)0-(CH2)m-;
or wherein X1 is -(CH2)n- or -CH.(M.€)-(CE^m- and
Y1 is -(CH^-NH^CH^-, -CO-(CH2)m-, -CONH-fCH^-, -C(=S)NH-(CH2)m-,
-CKOCMCH^- or -S(0)q-(CH2)M-;
or wherein X1 is -CH20, -CH2NH- or -OS2N((l-4C)aliyl)- and
Y1 is -CO-(CH2)M- -CONH-(CH2)m- or -C(=S)NB-(CH2)m- ; and additionally Y1 is

-S02- when X1 is -CH2NH- or -CH2N((l-4C)alkyl)-, and Y1 is -(CH2)M- when X1 is -CH20- or -CH2N((l-4C)alkyl)-; wherein n is 1,2 or 3; m is 0,1,2 or 3 and q is 0,1 or 2; and when Y1. is -(CH2)m-NH-(CH2)m- each m is independently selected from 0, 1, 2 or 3.
It is to be understood that when a value for -X1- is a two-atom link and is written, for example, as -CH2NH- it is the left hand part (-CH2- here) which is bonded to the group of formula (TAfl) to (TAf6) and the right hand part (-NH- here) which is bonded to -Y1- in the definition in (TAfc). Similarly, when -Y1- is a two-atom link and is written, for example, as -CONH- it is the left hand part of -Y1- (-CO- here) which is bonded to the right hand part of-X1-, and the right hand part of-Y1- (-NH- here) which is bonded to the AR2, AR2a, AR2b, AR3, AR3a or AR3b moiety in the definition in (TAfc).
Preferably R6 is hydrogen or (l-4C)alkyl, and R4 and R5 are independently selected from hydrogen, (l-4C)alkyl or one of R4 and R5 is selected from group (TAfa). Other preferable substituents on the (TAfl) to (TAf6) are illustrated in the accompanying Examples. Most preferable is (TAf2) with such preferable substituents.
(TAg) When T is a carbon linked tropol-3-one or tropol-4-one, optionally substituted in a position not adjacent to the linkitig position (TAg), it is preferably selected from a group of formula (TAgl), (TAg2) or (TAg3). The above preferred values of (TAg) are particularly preferred when present in Ql or QJ2, especially Ql.
0 R7

(TAgl) (TAg2) (TAg3)
wherein R7 is selected from
(TAga)hydrogen, (l-4C)alkyl {optionally substituted by one or two substituents (excluding
geminal ^'substitution) independently selected from fluoro, hydroxy, (I-4C)aIfcoxy and - •
NRvRw]}; or
(TAgb)RE-0-, R8-S-, R8-NH- or R.8R8-N-;
wherein R8 is selected (independently where appropriate) from hydrogen, (l-4C)alkyl or (3-

8C)cycloalkyl {both optionally substituted by one or two substituents (excluding geminal disubstitution) independently selected from hydroxy, (l-4C)alkoxy, (l-4C)alkoxycarbonyl and -NRvRw}, (2-4C)alkenyl {optionally substituted by one or two -NRvRw substituents}, (1 -4C)alkanoyl {optionally substituted by one or two substituents independently selected from -NRvRw and hydroxy}, phenyl-(l-4C)alkyl or pyridyl-(l-4C)alkyl {the phenyl and pyridyl (preferably pyridin-4-yl) rings being optionally substituted by one or two -NRvRw substituents}; or
(T^g^morpholino, thiomorpholino, pyrrolidino {optionally independently substituted in the 3- and/or 4-positions by (l-4C)alkyl}, piperidino substituted in the 4-position by R9-, R9-0-, R9-S-, R9~NH- or R^'-N-; wherein R9 is selected (independently where appropriate) from hydrogen, (l-4C)alkyl {optionally substituted by one or two (excluding geminal disubstitution) hydroxy, (l-4C)alkoxy, (l-4C)alkoxycarbonyl or-NRvRw} and piperazino {optionally substituted in the 4-position by (l-4C)alkyl, (3-8C)cycloallcyl, (l-4C)allcanoyl, (l-4C)alkoxycarbonyl or (l-4C)aIkylsulfonyl, and optionally independently substituted in the 3- and/or 5-positions by (l-4C)alkyl}; wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl.
(TC) Preferred values for the optional substituents and groups defined in (TCa) to (TCc) are defined by formulae (TCI) to (TC4) :-

(TCI) (TC2) (TC3) (TC4)
wherein in (TCI): >A3-B3- is >C(Rq)-CH(Rr)- and G is -Q-, -S-, -SO-, -S02- or >N(Rc); wherein in (TC2) : ml is 0,1 or 2; >A3-B3- is >C=C(Rr)- or >C(Rq)-CH(Rr)- and G is -0-, -S-, -SO-, -SO,- or >N(Rc);
wherein in (TC3): ml is 0,1 or 2; >A3-B3- is >C(Rq)-CH(Rr)- (other than when Rq and Rr are both together hydrogen) and G is -0-, -S-, -SO-, -S02- or >N(Rc); wherein in (TC4): nl is 1 or 2; ol is 1 or 2 and nl + ol = 2 or 3; >A3-B3- is >C=C(Rr)- or >C(Rq)-CH(Rr)- or >N-CH2- and G is -0-, -S-, -SO-, -S02- or >N(Rc); Rp is hydrogen, (1-

4C)aIkyl (other than when such substitution is defined by >A3-B3-), hydroxy, (l-4C)alkoxy or
(l-4C)aLkanoyloxy;
wherein in (TCI), (TC2) and (TC4); ml, nl and ol are as defined hereinbefore:
>A3-B3- is >N-CHr and G is >C(R")(R12), >C=0, >C-OH, >C-(l-4C)alkoxy, >C=N-OH,
>C=N-(l-4C)alkoxy, >C=N-NH-(l-4C)alkyl, >C=N-N((l-4C)alkyl)2 (the last two (1-
4C)alkyl groups above in G being optionally substituted by hydroxy) or >C=N-N-CO-(l-
4C)allcoxy; wherein > represents two single bonds;
Rqis hydrogen, hydroxy, halo, (l-4C)alkyl or (l-4C)alkanoyloxy;
Rr is (independently where appropriate) hydrogen or (l-4C)alkyl;
R" is hydrogen, (l-4C)alkyl, fluoro(l-4C)aIkyl, (l-4C)allcyl-thio-(l-4C)alkyl or hydroxy-(l-
4C)alkyl and R12 is -[C(Rr)(Rr)]^-N(Rr)(Rc) wherein m2 is 0,1 or 2;
and, other than the ring substitution defined by G, >A3-B3- and Rp, each ring system may be
optionally further substituted on a carbon atom not adjacent to the link at >A3- by up to two
substituents independently selected from (l~4C)alkyl, fluoro(l-4C)alkyl (including
trifluoromethyl), (l-4C)alkyl-thio-(l-4C)alkyl, hydroxy-(l-4C)alkyl, amino, amino-(l-
4C)alxyl, (l^C)alkanoylamino, (l-4C)alkanoylamino-(l-4C)alkyl, carboxy, (1-
4C)alkoxycarbonyl, AR-oxymethyl, AR-thiomethyl, oxo (=0) (other than when G is >N-Rc
and Re is group (Rc2) defined hereinbefore) or independently selected from Re; and also
hydroxy or halo (the last two optional substituents only when G is -0- or -S-);
wherein AR (or ARp) is as defined for formula (IP) hereinafter; Re is selected from groups
(Rcl) to (Rc5) defined hereinbefore.
For the avoidance of doubt, ( )rai, ( )ni and ()0l indicate (-CH2-)mi, (-CH2-)„i and (-CH,-)0l respectively (optionally substituted as described above).
In the above definition of (TCI) to (TC4) and of the further optional substituents, AR is preferably AR2, and the further optional substituents are preferably not selected from the values listed for Re. A preferred value for G is >N(Rc) or >C(Rn)(R12).
Particularly preferred values for the optional substituents and groups defined in (TCa) to (TCc), and (TCI) to (TC4) are contained in the following definitions (TC5) to (TCI 1):-

(TC5) (TC6) (TC7)

wherein Rc has any of the values listed hereinbefore or hereinafter.
Especially preferred are (TC5), (TC6), (TC7) and (TC9), most especially (TC5) in which Re has any of the values listed hereinbefore or hereinafter (especially R13CO- with the preferable R13 values given hereinafter). In (TC5) Rc is preferably selected from the group (Rc2), especially R13CO with the preferable R13 values given hereinafter. In (TC7) Rc is preferably selected from group (Rc3) or (Rc4).
The above preferred values of (TCa) to (TCc) are particularly preferred when present in Ql or Q2, especially Ql (especially when HET is isoxazole).
(TDa) When T is a bicyclic spiro-ring system as defined in (TDa), it is preferably selected from a group of formula (TDal) to (TDa9). The above preferred values of (TDa) are particularly preferred when present in Ql or Q2, especially Ql.

wherein;
(i) the A4 linking group is a nitrogen atom or an sp3 or sp2 carbon atom (with the double
bond, where appropriate, orientated in either direction); and
(ii) one of the ring carbon atoms at positions marked * and ** is replaced by one of the
following groups -NRc-, >CH-NHRc, >CH~NRc-(l-4C)alkyl, >CH-CH2-NHRc, >CH-CH2-
NRc-(l-4C)alkyl [wherein a central -CH2- chain link is optionally mono- or di-substituted by
(l-4C)alkyl]; with the provisos that positions marked * are not replaced by -NH- in the ring
containing the A, link when A4 is a nitrogen atom or an sp2 carbon atom, and that positions .
marked * are not replaced by -NH- in the three membered ring in (TDal), (TDa4) and (TDa5);
and
(iii) the ring system is optionally (further) substituted on an available ring carbon atom by
up to two substituents independently selected from (l-4C)alkyl, fluoro(l-4C)aIkyl (including
trifluoromethyl), (l-4C)aIkyl-thio-(l-4C)aIkyl, hydroxy-(l-4C)alkyl, amino, amino-(l-
4C)alkyl, (l-4C)a!kanoylamino,, (l-4C)alkanoylarnino-(l-4C)alkyl, cafboxy, (1-
4C)alkoxycarbonyl, AR2-oxymethyl, AR2-thiomethyl, oxo (=0) (other than when the ring
contains an >N-Rc and Re is group (Rc2)) and also hydroxy or halo;

wherein Re has any of the values listed hereinbefore or hereinafter.
(TDb) When T is a 7-, 8- or 9-membered bicyclic ring system containing a bridge of 1, 2 or 3 carbon atoms as defined in (TDb), it is preferably selected from a group defined by the ring skeletons shown in formulae (TDbl) to (TDb 14) :-

wherein;
(i) the ring system contains 0,1 or 2 ring nitrogen atoms (and optionally a further O or S
ring heteroatom),and when present the ring nitrogen, O or S heteroatom/s are at any position
other than as part of the 3-membered ring in (TDbl);
(ii) the ring system is linked via a ring nitrogen atom or a ring sp3 or sp2 carbon atom
(with the double bond, where appropriate, orientated in either direction) from any position in
either ring [other than from a bridgehead position or from an sp2 carbon atom in the 4-
membered ring in (TDb2), (TDb6) and (TDbl 1)];

(iii) one of the ring carbon atoms at a position not adjacent to the linking position, is replaced (other than when the ring contains an 0 or S heteroatom) by one of the following groups -NR.c- [not at a bridgehead position], >C(H)-NHRc, >C(H)-NRc-(l-4C)alkyl, >C(H)-CH2-NHRc, >C(H)-CH2-NRc-(l-4C)alkyl [wherein the hydrogen atom shown in brackets is not present when the replacement is made at a bridgehead position and wherein a central -CH2- chain link is optionally mono- or di-substituted by (l-4C)alkylJ; with the proviso that when the ring system is linked via a ring nitrogen atom or an sp2 carbon atom any replacement of a ring carbon atom by -NRc-, 0 or S is at least two carbon atoms away from the linking
position; and
(iv) the ring system is optionally (further) substituted on an available ring carbon atom as
for the bicyclic spiro-ring systems described in (TDa); wherein Re has any of the values listed
hereinbefore or hereinafter.
It will be appreciated that unstable anti-Bredt compounds are not contemplated in this
definition (i.e. compounds with stuctures (TDb3), (TDb4), (TDb7), (XDb8), (TDb9),
(TDM2), (TDbl3) and (TDbl4) in which an sp2 carbon atom is directed towards a bridgehead
position).
Particularly preferred values of (TDb) are the following structures of formula (TDb4),
(TDb8) and/or (TDb9); wherein Re has any of the values listed hereinbefore or hereinafter.
The above preferred values of (TDb) are particularly preferred when present in Ql or Q2,
In another embodiment there is provided a compound of formula (3) as defined by formula (IP) below:
especially Ql.

wherein
HET is an N-linked 5-membered heteroaryl ring, containing either (i) 1 to 3 farther nitrogen heteroatoms or (ii) a further heteroatom selected from O and S together with an optional further nitrogen heteroatom; which ring is optionally substituted on a C atom by an oxo or thioxo group; and/or the ring is optionally substituted on a C atom by 1 or 2 (l-4C)alkyl groups; and/or on an available nitrogen atom (provided that the ring is not thereby quaternised) by (l-4C)aUcyl; Qis

wherein:
R2 and R3 are independently hydrogen or fluoro;
R6p is hydrogen, (1^4C)alkylJ hydroxy, (l-4C)alkoxy or (2-4C)alkanoyloxy;
>A-B- is of the formula >OC(Ra)- , >CHCHRa-, >C(OH)CHRa- or >N-CH2-
(> represents two single bonds) wherein Ra is hydrogen or (1 -4C)alkyl;
DisO,S,SO, S02orNR7p;
R4p and R5p are independently oxo (=0) [but not when R7p is group (PC) below], (l-4C)allcylJ
(l-4C)alkanoylamino-(l-4C)alkyl, hydroxy-(l-4C)alkyl, carboxy, (l-4C)alkoxycarbonyl,
ARp-oxymethyl, ARp-thiomethyl (wherein ARp is as defined hereinbelow) or independently
as defined for R7p hereinbelow with the proviso that R4p and RSp are not phenyl, benzyl, ARp
(as defined hereinbelow), a tetraaole ring system, cyclopentyl or cyclohexyl; and when D is 0
or S, R4p and Rsp are additionally independently hydroxy or bromo;
wherein R7p is selected from (PA) to (PE) :-

(PA) hydrogen, cyano, 2-((l-4C)alkoxycarbonyl)ethenyl, 2-cyanoethenyl,
2-cyano-2-((l-4C)alkyl)ethenyl, 2-((1^4C)aIkylammocarbonyl)ethenyl; .
(PB) phenyl, benzyl, ARp (as defined hereinbelow) or a tetrazole ring system [optionally
mono-substituted in the 1- or 2- position of the tetrazole ring by (l-4C)alkyl, (2-4C)allcenyl,
(2-4C)alkynyl or (l-4C)alkanoyl] wherein the tetrazole ring system is joined to the nitrogen in
NR7p by a ring carbon atom;
(PC) R1CpCO-,R10pSO2-orR10pCS-
wherein R10p is selected from (PCa) to (PCf) :-
(PCa) ARp (as defined hereinbelow);
(PCb) cyclopentyl or cyclohexyl or l,3-dioxolan-4-yl or l,4-dioxan-2-yl or l,3-dioxan"4-yl
[optionally mono- or disubstituted by substituents independently selected from (l-4C)alkyl
(including geminal disubstitution), hydroxy (but excluding l,3-dioxolan-4-yl, l,4-dioxan-2-yl
and l,3-dioxan-4-yl substituted by hydroxy), (l-4C)alkoxy, (l-4C)alkylthio, acetamido,
(l-4C)alkanoyl, cyano and trifluoromethyl];
(PCc) hydrogen, (l«4C)alkoxycarbonyl, trifluoromethyl, amino, (l-4C)aU di((l-4C)altyl)arriino, 2-(5- or 6-membered heteroaryl)ethenyl, 2-(5- or 6-membered
(partially) hydrogenated heteroaryl)ethenyl, 2-phenylethenyl [wherein the heteroaryl or
phenyl substituent is optionally substituted on an available carbon atom by up to three
substituents independently selected from (l-4C)alkoxy, halo, cyano and (for the phenyl
substituent only) (l-4C)alkylsulfonylj;
(PCd) (l-10C)aIkyl [optionally substituted by one or more groups (including geminal
disubstitution) each independently selected from hydroxy and amino, or optionally
monosubstituted by cyano, halo, (MOQalkoxy, trifluoromethyl, (l-4C)alkoxy-(l-4C)alkoxy,
(l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxy,(l-4C)aUcanoyl,(l-4C)alkoxycarbonyl,
(l-4C)alkylamino, di((l-4C)alkyl)amino, (l-6C0alkanoylamino, (l-4C)aIkoxycarbonylamino,
HKl-4C)allkyl-N-(2-6C)alkanoylarnino, (l-4C)alkylS(0)pNH-,
(l-4C)alkylS(0)p((l-4C)alkyl)N-, fluoro(l-4C)alkylS(0)pNH-,
fluoro(l-4C)alkylS(0)p((l-4C)alkyl)N-,phosphono, (l-4C)alkoxy(hydroxy)phosphoryl,
di-(l-4C)alkoxyphosphoryl, (l-4C)alkylS(0)q-, phenyl, naphthyl, phenoxy, naphthoxy,
phenylamino, naphmylamino, phenylS(0)q-, naphthylS(0)q- [wherein said phenyl and
naphthyl groups are optionally substituted by up to three substituents independently selected

from (l-4C)alkoxy, halo and cyano], or CYp (as defined hereinbelow), wherein (where
appropriate) p is 1 or 2 and q is 0,1 or 2];
(PCe) RUpC(0)0(l-6C)alkyl wherein Rup is an optionally substituted 5- or 6-membered
heteroaryl, optionally substituted phenyl, (l-4C)a!kylamino, benzyloxy-(l-4C)alkyl or
optionally substituted (l-10C)alkyl;
(PCI) R12pO- wherein R12 p is benzyl or optionally substituted (1 -6C)alkyl;

(PD) RdOC(Re)=€H(C=0)-, RfC(=0)C(=0)-, REN==C(Rh)C(=0)- or RiNHC(Rj)=CHC(==0)-

wherein Rd is (l-6C)aIkyl, Re is hydrogen or (l-6C)alkyl, or Rd and Re together form a

(3-4C)alkylene chain, Rfis hydrogen, (l-6C)aIkyl, hydroxy(l-6C)alkyl,

(l-6C)alkoxy(l-6C)alkyl, amino, (l-4C)alkylamino,

di-(l-4C)alkylarnino, (l-6C)alkoxy, (l-6C)alkoxy(l-6C)alkoxy, hydroxy(2-6C)alkoxy,

(l-4C)alkylammo(2~6C)alkoxy, mXl-4C)alkylamino(2-6C)a]koxy, Rg is (l-6C)alkyl,

hydroxy or (l-6C)alkoxy, Rh is hydrogen or (l-6C)aIkyl, R is hydrogen, (l-6C)alkyl,

optionally substituted phenyl or an optionally substituted 5- or 6-membered heteroaryl [and

(partially) hydrogenated versions thereof] and RJ is hydrogen or (l-6Qalkyl;

(PE) R14PCH(R13P)(CH2)M wherein m is 0 or 1, R13p is fluoro, cyano, (l-4C)alkoxy,

(l-4C)alkylsulfonyl, (l-4C)alkoxycarbonyl or hydroxy, (provided that when m is 0, RI3p is not

fluoro or hydroxy) and R,4p is hydrogen or (l-4C)alkyl;

wherein ARp is optionally substituted phenyl, optionally substituted phenyl(l-4C)alkyl,

optionally substituted naphthyl, optionally substituted 5- or 6-membered heteroaryl;

wherein ARp is also an optionally substituted 5/6 or 6/6 bicyclic heteroaryl ring system, in

which the bicyclic heteroaryl ring systems may be linked via an atom in either of the rings

comprising the bicyclic system, and wherein botii the mono- and bicyclic heteroaryl ring

systems are linked via a ring carbon atom and may be (partially) hydrogenated;

wherein CYp is selected from:-

(i) 4-, 5- or 6-membered cycloalkyl ring;

(ii) 5- or 6-membered cycloalkenyl ring;

(iii) 5- or 6-membered heteroaryl, 5- or 6-membered heteroaryloxy, 5- or 6-membered

heteroaryl-S(0)q-, 5- or 6-membered heteroarylamino [and (partially) hydrogenated versions
thereof] and

(iv) 5/6 or 6/6 bicychc heteroaryl, 5/6 or 6/6 bicyclic heteroaryloxy, 5/6 or 6/6 bicychc
heteroaryl-S(0)q-, 5/6 or 6/6 bicychc heteroarylarnino [and (partially) hydrogenated versions
thereof];
wherein q is 0,1 or 2 and any of the aforementioned ring systems in CYp may be optionally
substituted by up to three substituents independently selected from halo,
(l-4C)alkyl [including geminal disubstitution when CYp is a cycloalkyl or cycloalkenyl ring],
acyl, oxo andnitro-(l-4C)alkyl; and pharmaceutically-acceptable salts thereof.
In this embodiment (IP) of the specification the term 'alkyl' includes straight chained and branched structures. For example,' (l-6C)alkyI includes propyl, isopropyl and tert-butyl. However, references to individual alkyl groups such as "propyl" are specific for the straight chained version only, and references to individual branched chain alkyl groups such as "isopropyl" are specific for the branched chain version only. A similar convention applies to other radicals, for example halo(l-4C)alkyl includes 1-bromoethyl and 2-bromoethyl.
In this embodiment (IP) of the specification a '5- or 6-membered heteroaryl' and 'heteroaryl (monocyclic) ring' means a 5- or 6-membered aryl ring wherein (unless stated otherwise) 1,2 or 3 of the ring atoms are selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5- or 6-membered heteroaryl ring systems are furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole and thiophene.
In this embodiment (IP) of the specification a l5/6 or 6/6 bicychc heteroaryl ring system' and 'heteroaryl (bicychc) ring' means an aromatic bicychc ring system comprising a 6-membered ring fused to either a 5 membered ring or another 6 membered ring, the bicychc ring system containing 1 to 4 heteroatoms selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5/6 and 6/6 bicychc ring systems are indole, benzofuran, benzoimidazole, benzothiophene, benzisothiazole, benzoxazole, benzisoxazole, pyridoimidazole, pyrimidoimidazole, quinoline, quinoxaline, quinazoline, phthalazine, cinnoline and naphthyridine.
In this embodiment (IP) of the specification a '4-, 5- or 6-membered cycloalkyl ring' means a cyclobutyl, cyclopentyl or cyclohexyl ring; and a '5- or 6-membered cycloalkenyl ring' a means cyclopentenyl or cyclohexenyl ring.

Particular optional substituents for alkyl, phenyl (and phenyl containing moieties) and naphthyl groups and ring carbon atoms in heteroaryl (mono or bicyclic) rings in Rllp, RI2p, R and ARp include halo, (l-4C)alkyl, hydroxy, nitro, carbamoyl, (l-4C)alkylcarbamoyl, di-((l-4C)alkyl)carbamoyl, cyano, trifluoromethyl, trifluoromethoxy, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-4C)alkylS(0)q-, (wherein q is 0,1 or 2), carboxy, (l-4Qalkoxycarbony}, (2-4C)alkenyl, (2-4C)alkynyl, (l-4C)aJkmoyl, (l-4C)alkoxy, (l-4C)alkylS(0)2amino, (l-4C)alkanoylamino, benzoylamino, benzoyl, phenyl (optionally substituted by up to three substituents selected from halo, (l-4C)alkoxy or cyano), furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene, hydroxyimino(l-4C)alkyl, (l-4C)alkoxyimmo(l-4C)alkyl, hydroxy-(l-4C)alkyl, halo-(l-4C)alkyl, nitro(l-4C)alkyl, amino(l-4C)aU bicyclic) rings in Rllp, R1 and ARp may be mono- or disubstituted on ring carbon atoms with substituents independently selected from the above list of particular optional substituents.
For the avoidance of doubt, phosphono is -P(0)(OH)2; (l-4C)alkoxy(hydroxy)-phosphoryl is amono-(l-4C)aIkoxy derivative of -0-P(0)(OH)2; and di-(l-4C)alkoxyphosphoryl is a di-(l-4C)alkoxy derivative of-O-P(0)(OH)2.
In this embodiment of formula (IP) a '5- or 6-membered heteroaryl' and 'heteroaryl (monocyclic) ring' means a 5- or 6-membered aryl ring wherein (unless stated otherwise) 1,2 or 3 of the ring atoms are selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5- or 6-membered heteroaryl ring systems are furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole and thiophene.
Particular examples of 5-membered heteroaryl rings containing 2 or 3 heteroatoms independently selected from N, 0 and S (with the proviso that there are no O-O, 0-S or S-S bonds; and in an alternative embodiment, also no N-S bonds) are pyrazole, imidazole, 1,2,3-triazole, 1,2,4-triazole, oxazole, isoxazole, thiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole; and also in an alternative embodiment, isothiazole, 1,2,5-thiadiazole, 1,2,4-thiadiazole or 1,2,3-thiadiazole.

In this embodiment of formula (IP) a '5/6 or 6/6 bicyclic heteroaryl ring system' and 'heteroaryl (bicychc) ring' means an aromatic bicyclic ring system comprising a 6-membered ring fused to either a 5 membered ring or another 6 membered ring, the bicyclic ring system containing 1 to 4 heteroatoms selected from nitrogen, oxygen and sulfur. Unless stated otherwise, such rings are fully aromatic. Particular examples of 5/6 and 6/6 bicyclic ring systems arc indole, benzofiiran, benzhmdazole, benzothiopheiie, benzisothiazole, benzoxazole, benzisoxazole, pytidoimidazole, pyrimidoimidazole, quinoline, quinoxaline, quinazoline, phthalazine, cinnoline and naphthyridine.
Particular optional substituents for alkyl, phenyl (and phenyl containing moieties) and naphthyl groups and ring carbon atoms in heteroaryl (mono or bicyclic) rings in R14p, R,5p, Ri and ARp include halo, (l-4C)alltyl, hydroxy, nitro, carbamoyl, (l-4C)alkylcarbamoyl, di-((l-4C)alkyl)carbamoyl, cyano, trifluoromethyl, trifluoromethoxy, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-4C)alkyl S(O) - (q is 0,1 or 2), carboxy, (l-4C)alkoxycarbonyl, (2-
4C)alkenyl, (2-4C)alkynyl, (l-4Qalkanoyl, (l-4C)alkoxy, (l-4C)alkylS(0)2amino, (1-4C)alkanoylarnino, benzoylamino, benzoyl, phenyl (optionally substituted by up to three substituents selected from halo, (l-4C)alkoxy or cyano), furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene, hydroxyirriino(l-4C)aIkyl, (MC)aUcoxyirnino(l-4C)alkyl, hydroxy-(l-4C)alkyl, halo-(l-4C)alkyl, nitro(l-4C)alkyl, amino(l-4C)alkyl, cyano(l-4C)alkyl, (l-4C)alkanesulfonamido, aminosulfonyl, (l-4C)alkylaminosulfonyl anddi-((l-4C)aHcyl)ammosulfonyl. The phenyl and naphthyl groups and heteroaryl (mono- or bicyclic) rings in R,4p, Ri and ARp may be mono- or di-substituted on ring carbon atoms with substituents independently selected from the above list of particular optional substituents.
In this specification the term 'alkyl' includes straight chained and branched structures. For example, (l-6C)alkyl includes propyl, isopropyl and tert-butyl. However, references to individual alkyl groups such as "propyl" are specific for the straight chained version only, and references to individual branched chain alkyl groups such as "isopropyl" are specific for the branched chain version only. A similar convention applies to other radicals, for example halo(l-4C)alkyl includes 1-bromoethyl and 2-bromoethyl.
There follow particular and suitable values for certain substituents and groups referred to in this specification. These values may be used where appropriate with any of the

definitions and embodiments disclosed hereinbefore, or hereinafter.
Examples of (l-4C)alkyl and (l-5C)alkyl include methyl, ethyl, propyl, isopropyl and t-butyl; examples of (l-6C)aIkyI include methyl, ethyl, propyl, isopropyl, t-butyl, pentyl and hexyl; examples of (l-lOC)alkyl include methyl, ethyl, propyl, isopropyl, pentyl, hexyl, heptyl, octyl andnonyl; examples of (l-4C)alkaiioyIamino-(l-4c) alkyl include formamidomethyl, acetamidomethyl and acetamidoethyl; examples of hydroxy(l-4C)alkyl and hydroxy(l-6C)aIkyI include hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl and 3-hydroxypropyl; examples of (l-4C)alkoxycarbonyl include methoxycarbonyl, ethoxycarbonyl and propoxycarbonyl; examples of 2-((l-4C)aIkoxycarbonyl)ethenyl include 2-(methoxycarbonyl)ethenyl and 2-(ethoxycarbonyl)ethenyl; examples of 2-cyano-2-((l-4C)alkyl)ethenyI include 2-cyano-2-methylethenyl and 2-cyano-2-ethylethenyl; examples of 2-nitro-2-((l-4C)aIkyl)ethenyl include 2-nitro-2-methylethenyl and 2-nitro-2-ethylethenyl; examples of 2-((l-4C)aIkylammocarbonyl)ethenyl include 2-(memylaminocarbonyl)ethenyl and2-(emylaminocarbonyl)ethenyl; examples of (2-4C)aIkenyI include allyl and vinyl; examples of (2-4C)aIkynyI include ethynyl and 2-propynyl; examples of (l-4C)aIkanoyl include formyl, acetyl and propionyl; examples of (1-4C)alkoxy include methoxy, ethoxy and propoxy; examples of (l-6C)aIkoxy and (1-lOQalkoxy include methoxy, ethoxy, propoxy and pentoxy; examples of (l-4C)aIkylthio include methylthio and ethylthio; examples of (l-4C)aIkylamino include methylamino, emylarnino and propylamino; examples of di-((l-4C)alkyl)amino include dimemylamino, N-ethyl-N-memylamino, diethylamino, N-memyl-N-propylamino and dipropylamino; examples of halo groups include fluoro, chloro andbromo; examples of (l-4C)alkylsulfonyl include methylsulfonyl and ethylsulfonyl; examples of (l-4C)allcoxy-(l-4Qalkoxy and (1-6C)alkoxy-(l-6C)aIkoxy include methoxymethoxy, 2-methoxyethoxy, 2-ethoxyethoxy and 3-methoxypropoxy; examples of
(l»4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxy include 2-(methoxymethoxy)ethoxy, 2-(2-methoxyethoxy)ethoxy; 3-(2-methoxyethoxy)propoxy and 2-(2-ethoxyethoxy)ethoxy; examples of (l-4C)aIkyIS(0)2amino include methylsulfonylamino and ethylsulfonylamino; examples of (l-4C)alkanoylamino and (l-6C)aIkanoylamrao include formamido, acetamido andpropionylamino; examples of (l-4C)alkoxycarbonyIamino include memoxycarbonylamino and emoxycarbonylamino; examples of N-(l-4C)aIkyl-N-(l-

oC)aiKanoyiamino include N-methylacetamido, N-ethylacetamido and N-methylpropionamido; examples of (l-4C)aIkylS(0)pNH- wherein p is 1 or 2 include memylsulfinylamino, methylsulfonylamino, emylsulfmylamino and ethylsulfonylamino; examples of (l-4C)alkylS(0)p((l-4C)aIkyl)N- wherein p is 1 or 2 include > melnylsulfinylmemylamino, memylsulfonylmethylamino, 2-(ethylsulfinyl)ethylamino and 2-(ethylsulfonyl)ethylamino; examples of fluoro(l-4C)aIkyIS(0)pNH- wherein p is 1 or 2 include trifluoromemylsulfmylamino and trifluoromethylsulfonylamino; examples of fluoro(l-4QaIkylS(0)p((l-4C)alkyI)NH- wherein p is 1 or 2 include trifluoromemylsuMnylmethylamino andtrifluoromemylsulfonylmemylamino examples of (1-4C)aIkoxy(hydroxy)phosphoryl include methoxy(hydroxy)phosphoryl and ethoxy(hydroxy)phosphoryl; examples of di-(l-4Qalkoxyphosphoryl include di-methoxyphosphoryl, di-ethoxyphosphoryl and ethoxy(methoxy)phosphoryl; examples of (1-4C)aIkylS(0)q- wherein q is 0,1 or 2 include methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl and ethylsulfonyl; examples of phenylS(0)q and
naphthyIS(0)q- wherein q is 0, l or 2 are phenylthio, phenylsulflnyl, phenylsulfonyl and naphthylthio, naphthylsulBnyl and naphthylsulfonyl respectively; examples of benzyloxy-(l-4QalkyI include benzyloxymethyl and benzyloxyethyl; examples of a (3-4C)aIkyIene chain are trimethylene or tetramethylene; examples of (l-6C)alkoxy-(l-6C)alkyI include methoxymethyl, ethoxymethyl and 2-methoxyethyl; examples of hydroxy-(2-6C)aIkoxy include 2-hydroxyethoxy and 3-hydroxypropoxy; examples of (l-4C)aIkylamino-(2-6C)alkoxy include 2-methylaminoethoxy and 2-ethylaminoethoxy; examples of di-(l-4C)aIkylamino-(2-6C)aIkoxy include 2-dimethylaminoethoxy and 2-diemylaminoethoxy; examples of phenyI(l-4C)alkyl include benzyl and phenethyl; examples of (1-4C)alkylcarbamoyl include memylcarbamoyl and ethylcarbamoyl; examples of di((l-4QaIkyl)carbamoyI include di(methyl)carbamoyl and di(ethyl)carbamoyl; examples of nydroxyimino(l-4C)aIkyl include hydroxyiminomethyl, 2-(hydroxyimino)ethyl and 1-(hydroxyimino)ethyl; examples of (l-4Qalkoxyimino-(l-4C)alkyl include memoxyiminomethyl, emoxyiminomethyl, l-(methoxyimino)ethyl and 2-(memoxyimino)ethyl; examples of halo(l-4C)alkyl include, halomethyl, 1-haloethyl, 2-haloethyl, and 3-halopropyl; examples of nitro(l-4C)aIkyI include nitromethyl, 1-nitroethyl, 2-nitroethyl and 3-nitropropyl; examples of ammo(l-4C)alkyl include aminomethyl, 1-

aminoethyl, 2-aminoethyl and 3~aminopropyl; examples of cyano(l-4C)alkyl include cyanomethyl, 1-cyanoethyl, 2-cyanoethyl and 3-cyanopropyl; examples of (1-4C)alkanesuIfonamido include methanesulfonamido and ethanesulfonamido; examples of (l-4C)alkylaininosuIfonyl include memylaminosulfonyl and emylarninosulfonyl; and examples of di-(l-4C)alkylaminosuIfonyl include dimemylaminosulfonyL diethylaminosulfonyl and N-methyl-N-ethylaminosulfonyl; examples of (1-4C)alkanesntfonyloxy include methylsulfonyloxy, ethylsulfonyloxy and propylsulfonyloxy; examples of (l-4C)alkanoyIoxy include acetoxy; examples of (l-4C)alkylaminocarbonyl include methylaminocarbonyl and ethylaminocarbonyl; examples of di((l-4C)alkyl)aminocarbonyl include dimemylaminocarbonyl and diemylaminocarbonyl; examples of (3-8C)cycIoalkyl include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl; examples of (4-7C)cycIoalkyl include cyclobutyl, cyclopentyl and cyclohexyl; examples of di(N-(l~4C)alkyl)aminomethylimino include dimethylarmnomethylimino and diethylammomemylimino.
Particular values for AR2 include, for example, for those AR2 containing one heteroatom, furan, pyrrole, thiophene; for those AR2 containing one to four N atoms, pyrazole, imidazole, pyridine, pyrimidine, pyrazine, pyridazine, 1,2,3- & 1,2,4-triazole and tetrazole; for those AR2 containing one N and one O atom, oxazole, isoxazole and oxazine; for those AR2 containing one N and one S atom, tbiazole and isothiazole; for those AR2 containing two N atoms and one S atom, 1,2,4- and 1,3,4-thiadiazole.
Particular examples of AR2a include, for example, dihydropyrrole (especially 2,5-dihydropyrrol-4-yl) and tetrahydropyridine (especially l,2,5,6-tetrahydropyrid-4-yl).
Particular examples of AR2b include, for example, tetrahydrofuran, pyrrolidine, morpholine (preferably morpholino), thiomorpholine (preferably thiomorpholino), piperazine (preferably piperazmo), imidazoline and piperidine, l,3-dioxolan-4-yl, l,3-dioxan-4-yl, 1,3-dioxan-5-yl and l,4-dioxan-2-yl.
Particular values for AR3 include, for example, bicyclic benzo-fused systems containing a 5- or 6-membered heteroaryl ring containing one nitrogen atom and optionally 1-3 further heteroatoms chosen from oxygen, sulfur and nitrogen. Specific examples of such ring systems include, for example, indole, benzofuran, benzothiophene, benzimidazole,

benzothiazole, benzisothiazole, benzoxazole, benzisoxazole, quinoline, quinoxaline, quinazoline, phthalazine and cinnoline.
Other particular examples of AR3 include 5/5-, 5/6 and 6/6 bicyclic ring systems containing heteroatoms in both of the rings. Specific examples of such ring systems include, for example, purine and naphthyridine.
Further particular examples of AR3 include bicyclic heteroaryl ring systems with at least one bridgehead nitrogen and optionally a further 1-3 heteroatoms chosen from oxygen, sulfur and nitrogen. Specific examples of such ring systems include, for example, 3H-pyrrolo[l,2-a]pyrrole, pyrrolo[2,l-b]thiazole, lH-imidazo[l,2-a]pyrroleJ lH-imidazo[l,2-a]imidazole5 lH,3H-pyrrolo[l,2-c]oxazole, lH-imidazo[l,5-a]pyrrole, pyrrolo[l,2-b]isoxazole, imidazo[5,l-b]thiazole, imidazo[2,l-b]thiazole, indolizine, imidazo[l,2-a]pyridine, imidazo[1,5-ajpyridine, pyrazolo[l,5-a]pyridine, pyrrolo[l,2-b]pyridazine, pyrrolo[l,2-c]pyrimidine, pyrrolo[l,2-a]pyrazme} pyirolo[l,2-a]pyrimidine, pyrido[2,l-c]-s-triazole, s-triazole[l,5-a]pyridine, inu^azo[l52-c]pyrimidine, imidazo[l,2-a]pyrazine, imidazo[l,2-a]pyrirnidine, imidazo[l,5-a]pyrazine, inn^azo[l,5-a]pyrimidine, imidazo[l,2-b]-pyridazine, s-triazolo[4}3-a]pyrimidine, imidazo[5,l-b]oxazole and imidazo[2,l-b]oxazole. Other specific examples of such ring systems include, for example, [lH]-pyrrolo[2,l-c]oxazine, [3H]-oxazolo[3,4-ajpyridine, [6H]-pyrrolo[2,l-c]oxazine andpyrido[2,l-c][l,4]oxazine. Other specific examples of 5/5- bicychc ring systems are imidazooxazole or imidazothiazole, in particular imidazo[5,l-b]thiazole, imidazo[2,l-b]thiazole, imidazo[5,l-b]oxazole or imidazo[2,l-b]oxazole.
Particular examples of AR3a and AR3b include, for example, indoline, l,3,4,6,9,9a-hexahydropyrido[2,lc][l,4]oxazin-8-yl, 1,2,3,5,8,8a-hexahydroimidazo[l,5a]pyridin-7-yl, l,5,8,8a-tetrahydrooxazolo[3,4a]pyridin-7-yl, l,5,6,7,8,8a-hexahydiooxazolo[3,4a]pyridm-7-yl,(7aS)[3H,5H]-l,7a-dihydropyrrolo[l,2c]oxazol-6-yl, (7aS)[5H]-l,2,3,7a-tetrahydropyrrolo[l,2c]imidazol-6-yl (7aR)[3H,5H]-l,7a-dihyd^opyrrolo[l,2c]oxazol-6-yl,t3H,5Hl-pyrrolo[l,2-c]oxazol-6-yl, [5H]-2,3-dmydropyrrolo[l,2-c]iniidazol-6-yl,[3H,5H]-pyrrolo[l,2-c]una2ol-6-yl, [3H,5H]-l,7a-dmydropyrrolo[l,2-c]thiazol-6-yl, [5H]-pyrrolo[l,2-c]imidazol-6-yl, [lH]-3,4,8,8a-

tetrahydropyrrolo[2,l-c]oxazm-7-yl, [3HJ-1,5,8a-tetrahydrooxazolo[3,4-a]pyrid-7yl,[3H]-5,8-dlhydroxazolo[3,4-a]pyrid-7-yl and5,8-dmydroiim\iazo[l,5-a]pyrid-7-yl.
Particular values for AR.4 include, for example, pyrrolo[a]quinoline, 2,3-pyrroloisoquinoline, pyrrolo[a]isoquinoline, lH-pyrrolo[l ,2-a]benzhrridazole, 9H-inudazo[l,2-a]indole, 5H-iinidazo[2,l-a]isoindole, lH-imidazo[3,4-a]indole, imidazo[l,2-a)quinoline, imdazo[2,l-a]isoqumolme, imidazollj-ajqumoline and imidazo[5,1 -a]isoquinoline.
Particular values of AR4a include partially hydrogenated version of those AR4 values listed immediately above.
The nomenclature used is that found in, for example, "Heterocyclic Compounds (Systems with bridgehead nitrogen), WX.Mosby (Ihtercsience Publishers Inc., New York), 1961, Parts 1 and 2.
Where optional substituents are listed such substitution is preferably not geminal disubstitution unless stated otherwise. If not stated elsewhere suitable optional substituents for a particular group are those as stated for similar groups herein.
Suitable substituents on AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 are (on ah available carbon atom) up to three substituents independently selected from (l-4C)alkyl {optionally substituted by (preferably one) substituents selected independently from hydroxy, trifluoromethyl, (l-4C)aIkyl S(0)q- (q is 0,1 or 2) (this last substituent preferably on AR1 only), (l-4C)alkoxy, (l-4C)alkoxycarbonyl, cyano, nitro, (1-4C)alkanoylamino, -CONRvRw or -NRvRw}, trifluoromethyl, hydroxy, halo, nitro, cyano, thiol, (l-4C)alkoxy, (l-4C)alkanoyloxy, d^ethylarmnomethyleneaminocarbonyl, di(N-(l-4C)allsyl)aminomemylimino, carboxy, (l-4C)alkoxycarbonyl, (l-4C)alkanoyl, (1-4C)alfylS02amino, (2-4C)alkenyl {optionally substituted by carboxy or (1-4C)alkoxycarbonyl}, (2-4C)alkynyl, (l-4C)alkanoylamino3 oxo (=0), thioxo (=S), (1-4C)alkanoylamino {the (l-4C)alkanoyl group being optionally substituted by hydroxy}, (1-4C)alkyl S(0)q- (q is 0, 1 or 2) (the (l-4C)alkyl group being optionally substituted by one or more groups independently selected from cyano, hydroxy and (l-4C)alkoxy}, -CONRvRw or -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl].
Further suitable substituents on AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 (on an available carbon atom), and also on alkyl groups (unless

indicated otherwise) are up to three substituents independently selected from trifluoromethoxy, benzoylamino, benzoyl, phenyl {optionally substituted by up to three substituents independently selected from halo, (l-4C)alkoxy or cyano}, ruran, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene, hydroxyimino(l-4C)alkyl, (l-4C)alkoxyimhio(l-4C)alkyl3 halo-(l-4C)alkyl, (l-4C)alkanesulfonamido, -S02NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkylj.
Preferable optional substituents on Ar2b as l,3-dioxolan-4-yl, l,3-dioxan-4-yl, 1,3-dioxan-5-yl or l,4-dioxan-2-yl are mono- or disubstitution by substituents independently selected from (l-4C)alkyl (including geminal disubstitution), (l-4C)alkoxy, (l-4C)alkylthio, acetamido, (l-4C)alkanoyl, cyano, trifluoromethyl and phenyl].
Preferable optional substituents on CY1 & CY2 are mono- or disubstitution by substituents independently selected from (l-4C)alkyl (including geminal disubstitution), hydroxy, (l-4C)alkoxy, (l-4C)alkylthio, acetamido, (l-4C)alkanoyl, cyano, and trifluoromethyl.
Suitable substituents on AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4 and AR4a are (on an available nitrogen atom, where such substitution does not result in quaternization) (1-4C)alkyl, (l-4C)alkanoyl {wherein the (l-4C)alkyl and (l-4C)alkanoyl groups are optionally substituted by (preferably one) substituents independently selected from cyano, hydroxy, nitro, trifluoromethyl, (l-4C)alkyl S(0)q- (q is 0,1 or 2), (l-4C)alkoxy, (1-4C)alkoxycarbonyL, (l-4C)alkanoylamino, -CONRvRw or -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl]}, (2-4C)alkenyl, (2-4C)alkynyl, (1-4C)alkoxycarbonyl or oxo (to form an N-oxide).
Suitable pharmaceutically-acceptable salts include acid addition salts such as methanesulfonate, furnarate, hydrochloride, citrate, maleate, tartrate and (less preferably) hydrobromide. Also suitable are salts formed with phosphoric and sulfuric acid. In another aspect suitable salts are base salts such as an alkali metal salt for example sodium, an alkaline earth metal salt for example calcium or magnesium, an organic amine salt for example triethylamine, morpholine, N-methylpiperidine, N-ethylpiperidine, procaine, dibenzylamine, N,N-diben2ylemylamine, tris-(2-hydVoxyemyl)amineJ N-methyl d-glucamine and amino acids such as lysine. There may be more than one cation or anion depending on the number of

charged functions and the valency of the cations or anions. A preferred pharmaceutically-acceptable salt is the sodium salt.
However, to facilitate isolation of the salt during preparation, salts which are less soluble in the chosen solvent may be preferred whether pharmaceutically-acceptable or not.
The compounds of the formula (I) may be administered in title form of a pro-drug which is broken down in the human or animal body to give a compound of the formula (I). A prodrug may be used to alter or improve the physical and/or pharmacokinetic profile of the parent compound and can be formed when the parent compound contains a suitable group or substituent which can be derivatised to form a prodrug. Examples of pro-drugs include in-vivo hydrolysable esters of a compound of the formula (J) or a pharmaceutically-acceptable salt thereof.
Various forms of prodrugs are known in the art, for examples see:
a) Design of Prodrugs, edited by H. Bundgaard, (Elsevier, 1985) and Methods in Enzymology, Vol. 42, p. 309-396, edited by K. Widder, et al (Academic Press, 1985);
b) A Textbook of Drug Design and Development, edited by Krogsgaard-Larsen and
H. Bundgaard, Chapter 5 "Design and Application of Prodrugs", by H. Bundgaard p. 113-191 (1991);
c) H. Bundgaard, Advanced Drug Delivery Reviews, 8,1-38 (1992);
d) H. Bundgaard, et al, Journal of Pharmaceutical Sciences, 22,285 (1988); and
e) N.Kalceya,et al., Chem Pharm Bull, 32, 692(1984).
An in-vivo hydrolysable ester of a compound of the formula (I) or a pharmaceutically-acceptable salt thereof containing carboxy or hydroxy group is, for example, a pharmaceutically-acceptable ester which is hydrolysed in the human or animal body to produce the parent acid or alcohol. Suitable pharmaceutically-acceptable esters for carboxy include (l-6C)alkoxymethyl esters for example methoxymethyl, (l-6C)allcanoyloxymethyl esters for example pivaloyloxymethyl, phthalidyl esters, (3-8C)cycloalkoxycarbonyloxy(l-6C)alkyl esters for example 1-cyclohexylcarbonyloxyethyl; l,3-dioxolan-2-onylmethyl esters for example 5-methyl-l,3-dioxolan-2-ylmethyl; and (l-6C)alkoxycarbonyloxyethyl esters for example 1-methoxycarbonyloxyethyl and may be formed at any carboxy group in the compounds of this invention.

An in-vivo iiydrolysable ester of a compound of the formula (I) or a pharmaceutically-acceptable salt thereof containing a hydroxy group or groups includes inorganic esters such as phosphate esters (including phosphoramidic cyclic esters) and a-acyloxyalkyl ethers and related compounds which as a result of the in-vivo hydrolysis of the ester breakdown to give the parent hydroxy group/s. Examples of a-acyloxyalkyl ethers include acetoxymethoxy and 2,2-dimethylpropionyloxymethoxy. A selection of in-vivo hydrolysable ester forming groups for hydroxy include (l-10C)alkanoyl, benzoyl, phenylacetyl and substituted benzoyl and phenylacetyl, (l-lOC)alkoxycafhonyl (to give alkyl carbonate esters), di-(l-4C)alkylcarbamoyl andH-(di-(K4C)aUcylan3inoethyl)-H-(l-4C)alkylcarbamoyl (to give carbamates), di-(l-4C)alkylamin0acetyl and carboxyacetyl. Examples of ring substituents on phenylacetyl and benzoyl include chloroniethyl or aminomethyl, (l-4C)alkylaminomethyl and di-((l-4C)alkyl)aminomethyl, and morpholino or piperazino linked from a ring nitrogen atom via a methylene linking group to the 3- or 4-position of the benzoyl ring.
Certain suitable in-vivo hydrolysable esters of a compound of the formula (T) are described within the definitions listed in this specification, for example esters described by the definition (Rc2d), and some groups within (Rc2c). Suitable in-vivo hydrolysable esters of a compound of the formula (T) are described as follows. For example, a 1,2-diol may be cyclised to form a cyclic ester of formula (PD1) or a pyrophosphate of formula (PD2) :

(fcDl) (PP2)
Particularly interesting ar^ such cyclised pro-drugs when the 1,2-diol is on a (1-4C)alkyl chain linked to a carbonyl group in a substituent of formula Re borne by a nitrogen atom in (TC4). Esters of compounds of formula (T) wherein the HO- function/s in (PD1) and (F&2) are protected? by (l~4C)allkyl) phenyl ar benzyl are useM intermediates for &e preparation of such pro-drugs.
Further in-vivo hydrolysable esters include phosphoramidic esters, and also compounds of formula (T) in which any free hydroxy group independently forms aphosphoryl

(npd is 1) or phosphiryl (npd is 0) ester of the formula (PD3):

Useful intermediates for the preparation of such esters include compounds containing a group/s of formula (PD3) in which either or both of the -OH groups in (PD3) is independently protected by (l-4C)alkyl (such compounds also being interesting compounds in their own right), phenyl or phenyl-(l-4C)alkyl (such phenyl groups being optionally substituted by 1 or 2 groups independently selected from (l-4C)alkyl, nitro, halo and (1-4C)alkoxy).
Thus, prodrugs containing groups such as (PD1), (PD2) and (PD3) may be prepared by reaction of a compound of formula (I) containing suitable hydroxy group/s with a suitably protected phosphorylating agent (for example, containing a chloro or dialtylamino leaving group), followed by oxidation (if necessary) and deprotection.
When a compound of formula (I) contains a number of free hydroxy group, those groups not being converted into a prodrug functionality may be protected (for example, using a t-butyl-dimethylsilyl group), and later deprotected. Also, enzymatic methods may be used to selectively phosphorylate or dephosphorylate alcohol functionalities.
Other interesting in-vivo hydrolysable esters include, for example, those in which Re is defined by, for example, R14C(0)0(l-6C)alkyI-CO- (wherein RI4is for example, benzyloxy-(l-4C)alkyl, or phenyl). Suitable substituents on a phenyl group in such esters include, for example, 4-(l-4C)piperazino-(l-4C)alkyl, piperazino-(l-4C)alkyl and morpholino-(l-4C)alkyl.
Where pharrnaceutically-acceptable salts of an in-vivo hydrolysable ester may be formed this is achieved by conventional techniques. Thus, for example, compounds containing a group of formula (PD1), (PD2) and/or (PD3) may ionise (partially or fully) to form salts with an appropriate number of counter-ions. Thus, by way of example, if an in-vivo hydrolysable ester prodrug of a compound of formula (I) contains two (PD3) groups, there are four HO-P- functionalities present in the overall molecule, each of which may form an

appropriate salt (i.e. the overall molecule may form, for example, a mono-, di-, tri- or tetra-sodium salt).
The compounds of the present invention have a chiral centre at the C-5 position of the oxazolidinone ring. The pharmaceutically active enantiomer is of the formula (IA):

The present invention includes the pure enantiomer depicted above or mixtures of the 5R and 5S enantiomers, for example a racemic mixture. If a mixture of enantiomers is used, a larger amount (depending upon the ratio of the enantiomers) will be required to achieve the same effect as the same weight of the pharmaceutically active enantiomer. For the avoidance of doubt the enantiomer depicted above is generally the 5(R) enantiomer, although certain compounds (such as HET as pyrid-2-one) are the 5(S) enantiomer. Examples of 5(S) compounds are illustrated in the accompanying non-limiting Examples.
Furthermore, some compounds of the formula (I) may have other chiral centres. It is to be understood that the invention encompasses all such optical and diastereo-isomers, and racemic mixtures, that possess antibacterial activity. It is well known in the art how to prepare optically-active forms (for example by resolution of the racemic form by recrystallisation techniques, by chiral synthesis, by enzymatic resolution, by biotransformation or by chromatographic separation) and how to determine antibacterial activity as described hereinafter.
The invention relates to all tautomeric forms of the compounds of the formula (I) that possess antibacterial activity.
It is also to be understood that certain compounds of the formula (I) can exist in solvated as well as unsolvated forms such as, for example, hydrated forms. It is to be understood that the invention encompasses all such solvated forms which possess antibacterial

activity.
It is also to be understood that certain compounds of the formula (I) may exhibit polymorphism, and that the invention encompasses all such forms which possess antibacterial activity.
As stated before, we have discovered a range of compounds that have good activity against a broad range of Gram-positive pathogens including organisms known to be resistant to most commonly used antibiotics. Physical and/or pharmacokinetic properties, for example increased stability to mammalian peptidase metabolism and a favourable toxicological profile are important features. Xhe following compounds possess favourable physical and/or pharmacokinetic properties and are preferred.
Particularly preferred compounds of the invention comprise a compound of formula (I) or of formula (IP), or a pharmaceutically-acceptable salt or an in-vivo hydrolysable ester thereof, wherein the substituents Q, HEX, T and other substituents mentioned above have values disclosed hereinbefore, or any of the following values (which may be used where appropriate with any of the definitions and embodiments disclosed hereinbefore or hereinafter):
Preferably Q is selected from Ql, Q2, Q4, Q6 and Q9; especially Ql, Q2 and Q9; more particularly Ql and Q2; and most preferably Q is Ql.
Preferably X is selected from (XAf), (XDb) or (XC); especially groups (TAG), (XCb) and (XCc); more particularly (XC2), (XC3) and (XC4); and most preferably (XC5), (XC7) or (XC9), and most particularly (XC9) and (XC5). Especially preferred is each of these values of X when present in Ql and Q2, particularly in Ql.
Preferable values for other substituents (which may be used where appropriate with any of the definitions and embodiments disclosed hereinbefore or hereinafter) are :-(aO) In. one embodiment HEX is a 6-membered heteroaryl ring as defined herein, and in another embodiment HEX is a 5-membered heteroaryl ring as defined herein. Preferably HEX is a 5-membered heteroaryl as defined herein.
In this specification it will be appreciated that when HEX is a 5-membered heteroaryl ring, the ring must be aromatic and that when HEX is a 6-membered heteroaryl ring, the ring system (which contains the optimum number of double bonds) can necessarily only be pseudoaromatic. It will also be appreciated that when HEX as an N-linked 5-membered

heteroaryl ring is optionally substituted on an available carbon atom by oxo or tbioxo then, when HEX contains 1 to 3 further nitrogen heteroatoms, one of the further nitrogen heteroatoms is present as NH or as N-(l-4C)alkyl. Similarly, when HEX as an N-linked 5-membered heteroaryl ring is optionally substituted on an available nitrogen atom by (1-4C)alkyl then the ring is substituted on an available carbon atom by oxo or thioxo.
(a) When HEX is a 6-membered heteroaryl as defined herein, preferably HEX is pyridine or pyridazine; preferably with a 2-oxo substituent.
(b) When HEX is a 5-membered heteroaryl as defined herein, preferably HEX contains only nitrogen heteroatoms or is thiadiazole or thiazole.
> (c) Yet more preferably HEX is triazole, tetrazole or imidazole, especially triazole or tetrazole, and most especially triazole.
(d) Further preferred as HEX is 1,2,3-triazole and 1,2,4-triazole, especially 1,2,3-triazole, and most especially 1,2,3-triazol-l-yl.
(e) Further preferred as HEX is 1,2,3,4-tetrazole, especially l,2,3,4-tetrazol-2-yl.
(f) Most preferred is HET as 1,2,3-triazol-l-yl.
(g) Preferably HEX (when a 5-membered ring) is unsubstituted. (h) Preferably R6p is hydrogen;
(i) Preferably R4p and R5p are independently selected from hydrogen, (l-4C)alkyl,
carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (l-4C)alkoxymethyl or carbamoyl;
(j) More preferably R4p and R5p are hydrogen;
(k) Preferably R2 and R3 are hydrogen or fluoro;
(1) In one aspect of the invention more preferably one of R2 and R3 is hydrogen and the
other fluoro. In another aspect of the invention both R2 and R3 are fluoro;
(m) Preferably >A-B- is of the formula >C=CH- (i.e. Ra is preferably hydrogen)
or>N-CH2-;
(n) Preferably D is 0 or NR7p;
(o) Preferably R7p is ARp, R10pCO-, RI0pSO2-, R10pCS-;
(p) More preferably R7p is ARp (most preferably benzyl, pyrimidyl, pyridinyl, pyridazinyl
or pyrazinyl) or R10pCO-;
(q) Particularly R7p is R10pCO-;

(ql) Especially preferred is R10pCO- (or R13CO-) wherein R10p (or R13) is (l-lO)alkyl
optionally substituted by hydroxy or (l-4C)alkylS(0)q- (wherein q is 0,1 or 2), wherein the
(l-4C)alkyl group is optionally substituted as defined herein for this particular substituent;
(r) Preferably ARp is 5- or 6-membered heteroaryl; more preferably ARp is 6-membered
heteroaryl, such as pyridinyl;
(s) Preferred substituents for phenyl and carbon atoms in heteroaryl (mono- and bicyclic)
ring systems in ARp, Rllp and R1 include halo, (l-4C)alkyl, hydroxy, nitro, amino, cyano,
(l-4C)alkylS(0)p- and (l-4C)alkoxy;
(t) Preferably the optionally substituted ring systems in ARp, R1 lp and R1 are
unsubstituted;
(u) In another embodiment in the definition of R10p in (PC) of embodiment (IP), 1,3-
dioxolan-4-yl and l,4-dioxan-2-yl are excluded.
(v) In one aspect of the invention, preferably R10p is (l-4C)alkoxycarbonyl,
hydroxy(l-4C)alkyl, (l-4C)alkyl (optionally substituted by one or two hydroxy groups, or by
an (l-4C)alkanoyl group), (l-4C)alkylamino, dimemylamino(l-4C)allcyl,
(L-4C)alkoxymethyl, (l-4C)alkanoylmethyl, (l-4C)alkanoyloxy(l-4C)alkyl, (l-5C)alkoxy or
2-cyanoethyl;
(w) In one aspect of the invention, more preferably R10p is 1,2-dihydroxyethyl,
l,3-dihydroxyprop-2-yl, 1,2,3-trihydroxyprop-l-yl, methoxycarbonyl, hydroxymethyl,
methyl, memylamino, dimemylaminomethyl, methoxymethyl, acetoxymethyl, methoxy,
methylthio, naphthyl, tert-butoxy or 2rcyanoethyl;
(x) In one aspect of the invention, particularly R10p is 1,2-dihydroxyethyl,
l,3-dihydroxyprop-2-yl or 1,2,3-trihydroxyprop-l-yl;
(y) In another aspect of the invention preferably R10p is hydrogen, (1-1 OQalkyl [optionally
substituted by one or more hydroxy] or RllpC(0)0(l-6C)alkyl.
(z) In another aspect of the invention, more preferably R10p is hydrogen, hydroxymethyl,
1,2-dihydroxyethyl or acteoxyacetyl; and/or Rc2c is (l-10C)alkyl optionally substituted by (1-
4C)alkyl S(0)q-(q is 0-2), optionally substituted as in claim 1.
(aa) Preferably Rup is (1-1 OQalkyl;

. (ab) Preferred optional substituents for (1 -10C)aliyl in Rllp are hydroxy, cyano, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino9 (l-4C)alkylS(0)p (wherein p is 1 or 2), carboxy, (l-4C)alkoxycarbonyl, (l-4C)alkoxy, piperazino or morpholino;
(m) Preferred optional substituents for (1 -6C)alkyl in R12p are hydroxy, (1 -4C)alkoxy, cyano, amino, (l-4C)all{ylamino, di((l-2C)alkyl)amino, (l-4C)alkylS(0)p- (wherein p is 1 or 2);
(n) Preferably 5- or 6-membered heteroaryl in Rllp is pyridinyl or imidazoH-yl;
(o) Preferably R12p is (l-6C)alkyl; most preferably R,2p is lert-butyl or methyl; (at) Preferably R13p is cyano or fluoro;
(ag) Preferably R,4p is hydrogen;
(ah) Preferably CYp is naphthoxy, especially naphth-1 -oxy or naphth-2-oxy.
Where preferable values are given for substituents in a compound of formula (IP), the corresponding substituents in a compound of formula (I) have the same preferable values (thus, for example, Re and R13 in formula (I) correspond with R7p and R,0p in formula (DP), and similarly for groups D and G). The preferred values of R7*1, for example, defined with reference to (IP) are also preferred values of Re and may be used as preferred values of Re in any compound of formula (I). For compounds of formula (T) preferred values for Re are those in group (Rc2) when present in any of the definitions herein containing Re - for example when present in compounds in which there is a (TC5) or (TC9) ring system. The preferred values for R10p listed above for compounds of formula (D?) are also preferred values for R13 in compounds of formula (I). In the definition of (Rc2c) the AR2a, AR2b, AR3a and AR3b versions of AR2 and AR3 containing groups are preferably excluded.
Particularly, HET (when substituted) is selected from the following 7 rings (HET-P1 to HET-P7) :-

The above HET definitions are especially preferred in embodiment (IP). Especially preferred compounds of the present invention are of the formula (EB):

wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fiuoro; and Rpl and Rp2 are independently hydrogen, hydroxy, bromo, (l-4C)alkyl, carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (1-4C)alkoxymethyl or carbamoyl; or pharmaceutically-acceptable salts thereof.
Further especially preferred compounds of the invention are of the formula (IB) wherein HET is wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fiuoro; and Rpl and Rp2 are independently hydrogen, AR-oxymethyl or AR-thiomethyl (wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrirnidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene); or pharmaceutically-acceptable salts thereof.
Of the above especially preferred compounds of the invention of the formula (IB), particularly preferred compounds are those wherein Rpl and Rp2 are hydrogen are particularly preferred.
Further especially preferred compounds of the present invention are of the formula (T3-1):

(IB-1)
wherein HET is triazole or tetrazole, and most especially triazole (particularly 1,2,3-triazole, and especially 1,2,3-triazoI-l-yI); R2 and R3 are independently hydrogen or fluoro and p is 1 or 2.
Further, especially preferred compounds of the invention are of the formula (IC):
Rp1 R2

(IC)
wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are independently hydrogen, AR-oxymethyl or AR-thiomethyl (wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene), (l-4C)allcyl, carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (1-4C)alkoxymethyl or carbamoyl and Rep is cyano, pyrimidin-2-yl, 2-cyanoethenyl, 2-cyano-2- ((l-4C)allcyl)ethenyl or Rep is of the formula R10pCO-, R10pSO2- or R,0pCS- (wherein R10p is hydrogen, (l-5C)alkyl [optionally substituted by one or more groups each independently selected from hydroxy and amino, or optionally monosubstituted by (l-4C)alkoxy, (1-4C)alkylS(0)q-, (l-4C)alkylarnino, (l-4C)alkanoyl, naphthoxy, (2-6C)aUcanoylamino or (1-4C)alkylS(0)pNH- wherein p is 1 or 2 and q is 0,1 or 2], imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, pyridoimidazole,
pyrimidoimidazole, quinoxaline, quinazoline, phthalazine, cinnoline or naphthyridine, or R10p is of the formula RllpC(0)0(l-6C)alkyl wherein Rllp is (l-6C)allcyl), or Rep is of the formula RfC(=0)C(=0)- wherein Rf is (l-6C)alkoxy; orpharmaceutically-acceptable salts thereof.

Of the above especially preferred compounds of the invention of the formula (IC), ' those wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are independently hydrogen, AR-oxymethyl or AR-thiomethyl (wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrirnidine, pyiidazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene), (l-4C)alkyl, carboxy, (l-4C)alkoxycarbonyl, hydroxymethyl, (1-4C)aIkoxymethyl or carbamoyl and Rep is cyano, pyrirnidin-2-yl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl or Rep is of the formula R10pCO-, R,0pSO2- or R10pCS- (wherein R,10p is hydrogen, (l-5C)alkyl [optionally substituted by one or more groups each independently selected from hydroxy and amino, or optionally monosubstituted by (l-4C)alkoxy, (1-4C)alkylS(0)q, (l-4C)alkylarnino, (l-4C)alkanoyl, (2-6C)alkanoylamino or (1-4C)alkylS(0)pNH- wherein p is 1 or 2 and q is 0,1 or 2], pyridine, or R10p is of the formula RllpC(0)0(l-6C)allcyl wherein RUp is (l-6C)alkyl), or Rep is of the formula RfC(=0)C(=0)-whereinRf is (l-6C)alkoxy; or pharmaceutically-acceptable salts thereof are further preferred.
Of the above especially preferred compounds of the invention of the formula (IC), particularly preferred compounds are those wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are hydrogen, and Rep is pyridin-2-yl (optionally substituted with cyano) or Rcp is of the formula R10pCO- (wherein R10p is hydrogen, l,3-dioxolan-4-yl (optionally disubstituted with (1-4C)alkyl) or (l-5C)allkyl [optionally substituted by one or more hydroxy groups] or R10p is of the formula RllpC(0)0(l-6C)alkyl wherein R11p is (l-6C)alkyl)); or pharmaceutically-acceptable salts thereof.
Of the above especially preferred compounds of the invention of the formula (IC), particularly preferred compounds are those wherein Rep is of the formula R10pCO- (wherein R10p is hydrogen, l,3-dioxolan-4-yl (optionally disubstituted with (l-4C)alkyl) or (l-5C)alkyl [substituted by two hydroxy groups, e.g. 2,3-dihydroxypropanoyl or by one hydroxy group, e.g. hydroxyacetyl]; or pharmaceutically-acceptable salts thereof.
In another aspect of the invention particularly preferred compounds of the invention are of the formula (IC) wherein HET is triazole or tetrazole, and most especially triazole; R2 and R3 are independently hydrogen or fluoro; Rpl and Rp2 are hydrogen and Rep is R10pCO-(wherein R10p is hydrogen, (l-5C)alkyl [optionally substituted by one or two hydroxy groups],

or Rl0p is of the formula RllpC(0)0(l-6C)alkyl (wherein RUp is (l-6C)alkyl)); and pharmaceutically-acceptable salts thereof.
In another aspect of the invention all of the compounds of formula (IB) or (IC) described above are further preferred when HET is triazole.
In yet another aspect the invention relates to all of the compounds of formula (IB) or (IC) described above wherein HET is 1,2,3-triazoM-yl.
In another aspect of the invention there are provided preferred compounds of the formula (IP) wherein HET is triazole or tetrazole, and most especially triazole; >A-B- is >N-CH2- and D is NR7p (or D is O) wherein Rep is a 6-membered heteroaiyl ring containing 1,2 or 3 ring nitrogen atoms as the only ring heteroatoms, linked via a ring carbon atom and optionally substituted on a ring carbon atom by one, two or three substituents independently selected from (l-4C)alkyl, halo, trifluoromethyl, (l-4C)alkyl S(0)q- (wherein q is 0,1 or 2), (l-4C)aIkylS(0)2amino, (l-4C)aUcanoylarnino, carboxy, hydroxy, amino, (l-4C)alkylairiino, di-(l-4C)altylamino, (MQalkoxycarbonyl, carbamoyl, K-(l-4C)alkylcarbamoyl, di-(N-(l-4C)aIkyl)carbamoyl, (l-4C)alkoxy, cyano or nitro; or pharmaceutically-acceptable salts thereof.
In yet another aspect the invention relates to all of the compounds of formula (IP) described immediately above wherein >A-B- is >N-CH2- and D is NR7p and wherein HET is triazole or tetrazole, and most especially triazole.
In all of the above aspects and preferred compounds of formula (IB) or (IC), in-vivo hydrolysable esters are preferred where appropriate, especially phosphoryl esters (as defined by formula (PD3) with npd as 1).
In all of the above definitions the preferred compounds are as shown in formula (IA), i.e. the pharmaceutically active (5(R)) enantiomer.
Particular compounds of the present invention include the compounds of Examples 34b, 44a, 52, 54,56, 58, 64 and 74 (wherein "a" refers to the first named compound, and "b" the second named compound in the Example title); or pharmaceutically-acceptable salts thereof. Particularly preferred salts are the sodium salts. In-vivo hydrolysable esters, or pharmaceutically-acceptable salts thereof, of Examples with hydroxy groups are also preferred, especially phosphoryl esters.

In a further aspect the present invention provides a process for preparing a compound of formula (I) or a pharmaceutically-acceptable salt or an in-vivo hydrolysable ester thereof. It will be appreciated that during certain of the following processes certain substituents may require protection to prevent their undesired reaction. The skilled chemist will appreciate when such protection is required, and how such protecting groups may be put in place, and later removed.
For examples of protecting groups see one of the many general texts on the subject, for example, 'Protective Groups in Organic Synthesis' by Theodora Green (publisher: John Wiley
»
& Sons). Protecting groups may be removed by any convenient method as described in the literature or known to the skilled chemist as appropriate for the removal of the protecting group in question, such methods being chosen so as to effect removal of the protecting group with minimum disturbance of groups elsewhere in the molecule.
Thus, if reactants include, for example, groups such as amino, carboxy or hydroxy it may be desirable to protect the group in some of the reactions mentioned herein.
A suitable protecting group for an amino or alkylamino group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an alkoxycarbonyl group, for example a methoxycarbonyl, ethoxycarbonyl or /-butoxycarbonyl group, an aiylmethoxycarbonyl group, for example benzyloxycarbonyl, or an aroyl group, for example benzoyl. The deprotection conditions for the above protecting groups necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or alkoxycarbonyl group or an aroyl group may be removed for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide. Alternatively an acyl group such as a f-butoxycarbonyl group may be removed, for example, by treatment with a suitable acid as hydrochloric, sulfuric or phosphoric acid or trifluoroacetic acid and an arylmethoxycarbonyl group such as a benzyloxycarbonyl group may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon, or by treatment with a Lewis acid for example boron tris(rrifluoroacetate). A suitable alternative protecting group for a primary amino group is, for example, a phthaloyl group which may be removed by treatment with an alkylamine, for example dimemylammopropylamine, or with hydrazine.

A suitable protecting group for a hydroxy group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an aroyl group, for example benzoyl, or an arylmethyl group, for example benzyl. The deprotection conditions for the above protecting groups will necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or an aroyl group may be removed, for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example Hthium or sodium hydroxide. Alternatively an arylmethyl group such as a benzyl group may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon.
A suitable protecting group for a carboxy group is, for example, an esterifying group, for example a methyl or an ethyl group which may be removed, for example, by hydrolysis with a base such as sodium hydroxide, or for example a f-butyl group which may be removed, for example, by treatment with an acid, for example an organic acid such as trifiuoroacetic acid, or for example a benzyl group which may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon.
Resins may also be used as a protecting group.
The protecting groups may be removed at any convenient stage in the synthesis using conventional techniques well known in the chemical art.
A compound of the formula (I), or a pharmaceutically-acceptable salt or an in vivo hydrolysable ester thereof, may be prepared by any process known to be applicable to the preparation of chemically-related compounds. Such processes, when used to prepare a compound of the formula (I), or a pharmaceutically-acceptable salt or an in vivo hydrolysable ester thereof, are provided as a further feature of the invention and are illustrated by the following representative examples. Necessary starting materials may be obtained by standard procedures of organic chemistry (see, for example, Advanced Organic Chemistry (Wiley-[nterscience), Jerry March). The preparation of such starting materials is described within the accompanying non-limiting Examples (in which, for example, 3,5-difluorophenyl, 3-Quorophenyl and (des-fluoro)phenyl containing intermediates may all be prepared by malagous procedures; or by alternative procedures - for example, the preparation of (T jroup)-(fluoro)phenyl intermediates by reaction of a (fluoro)phenylstannane with, for jxample, a pyran or (tetrahydro)pyridine compound, may also be prepared by anion chemistry see, for example, WO97/30995). Alternatively, necessary starting materials are obtainable by

analogous procedures to those illustrated which are within the ordinary skill of an organic chemist. Information on the preparation of necessary starting materials or related compounds (which may be adapted to form necessary starting materials) may also be found in the following Patent and Application Publications, the contents of the relevant process sections of which are hereby incorporated herein by reference :
WO99/02525; W098/54161; WO97/37980; WO97/30981 (& US5,736,545); WO97/21708 (& US5,719,154); WO97/10223; WO97/09328; W096V35691; W096/23788; WO96/15130; WO96/13502; WO95/25106 (& US5,668,286); W095/14684 (& US5,652,238); WO95/07271 (& USS,688,792); W094/13649; WO94/01110; W093/23384 (& US5,547,950 & US 5,700,799); WO93/09103 (&US5,565,571, US5,654,428, US5,654,435, US5,756,732 & US5,801,246); US5,231,188; US5,247,090; US5,523,403; W097/27188; WO97/30995; W097/31917; WO98/01447; WO98/01446; WO99/10342; WO99/10343; W099/11642; W099/64416; W099/64417 and GB99/03299;
European Patent Application Nos. 0,359,418 and 0,609,905; 0,693,491 Al (& US5,698,574); 0,694,543 Al (& AU 24985/95); 0,694,544 Al (& CA 2,154,024); 0,697,412 Al (& US5,529,998); 0,738,726 Al (& AU 50735/96); 0,785,201 Al (& AU 10123/97); German Patent Application Nos. DE 195 14 313 Al (& US5,529,998); DE 196 01 264 Al (& AU 10098/97); DE 196 01 265 Al (& AU 10097/97); DE 196 04 223 Al (& AU 12516/97); DE 196 49 095 Al (& AU 12517/97).
The following Patent and Application Publications may also provide useful information and the contents of the relevant process sections are hereby incorporated herein by reference :
FR 2458547; FR2500450(& GB 2094299, GB 2141716 & US 4,476,136); DE 2923295 (& GB 2028306, GB 2054575, US4,287,351, US4,348,393, US4,413,001, US4,435,415 & US4,526,786), DE 3017499 (& GB 2053196, US4,346,102 & US4,372,967); US4,705,799; European Patent Application Nos. 0,312,000; 0,127,902; 0,184,170; 0,352,781; 0,316,594;
The skilled organic chemist will be able to use and adapt the information contained and referenced within the above references, and accompanying Examples therein and also the Examples herein, to obtain necessary starting materials, and products.
Thus, the present invention also provides that the compounds of the formulae (!) and pharmaceutically-acceptable salts and in vivo hydrolysable esters thereof, can be prepared by a

process (a) to (d) as follows (wherein the variables are as defined above unless otherwise
stated):
(wherein the variables are as defined above unless otherwise stated) :
(a) by modifying a substituent in or introducing a substituent into another compound of formula (E);
(b) by reaction of a compound of formula (IT):

wherein Y is a displaceable group (which may be preformed, such as chloro or mesylate, or generated in-situ, for example under Mitsunobu conditions) with a compound of the formula (TO) :
HET
OH) wherein HET is HET-H free-base form or HET- anion formed from the free base form; or .
(c) by reaction of a compound of the formula (TV) :
Q-Z dV) wherein Z is an isocyanate, amine or urethane group with an epoxide of the formula (V) :

(d) For the 1,2,3-triazoles there is the additional possibility by cycloaddition via the azide
(wherein Y in (II) is azide);
and thereafter if necessary: (i) removing any protecting groups; (ii) forming a pharmaceuticaUy-acceptable salt; (iii) forming an in-vivo hydrolysable ester.
The main synthetic routes are illustrated in the Scheme below (with Q as phenyl, and X, R and A defined with reference to analogous substituents defined elsewhere herein). The

compounds of the invention maybe prepared by analogous chemistry adapted from this Scheme. The Scheme also shows the preparation of 1,2,3-triazoles via the azide (prepared from the relevant hydroxy compound).

Deprotection, salt formation or in-vivo hydrolysable ester formation may each be provided as a specific final process step.
The N-linked hetereocycle can of course be prepared early in the overall synthesis, and then other functional groups changed.

Where Y is a displaceable group, suitable values for Y are for example, a halogeno or sulfonyloxy group, for example a chloro, bromo, methanesulfonyloxy or toluene-4-. sulfonyloxy group.
General guidance on reaction conditions and reagents may be obtained in Advanced Organic Chemistry, 4th Edition, Jerry March (publisher : J.Wiley & Sons), 1992. Necessary starting materials may be obtained by standard procedures of organic chemistry, such as described in this process section, in the Examples section or by analogous procedures within the ordinary skill of an organic chemist. Certain references are also provided which describe the preparation of certain suitable starting materials, for example International Patent Application Publication No. WO 97/37980, the contents of which are incorporated here by reference. Processes analogous to those described in the references may also be used by the ordinary organic chemist to obtain necessary starting materials.
(a) Methods for converting substituents into other substituents are known in the art. For example an alkylthio group may be oxidised to an alkylsulfinyl or alkysulfonyl group, a cyano group reduced to an amino group, a nitro group reduced to an amino group, a hydroxy group alkylated to a methoxy group, a hydroxy group thiomethylated to an arylthiomethyl or a heteroarylthiomethyl group (see, for example, TetXett., 585,1972), a carbonyl group converted to a thiocarbonyl group (eg. using Lawsson's reagent) or a bromo group converted to an alkylthio group. It is also possible to convert one Re group into another Re group as a final step in the preparation of a compound of the formula (I), for example, acylation of a group of formula (TC5) wherein Re is hydrogen.
(b)( i) Reaction (b)(i) (in which Y is initially hydroxy) is performed under Mitsunobu conditions, for example, in the presence of tri-n-butylphosphine and diethyl azodicarboxylate (DEAD) in an organic solvent such as THF, and in the temperature range 0°C - 60°C, but preferably at ambient temperature. Details of Mitsunobu reactions are contained in Tet. Letts., 21,699, (1990); The Mitsunobu Reaction, D.L.Hughes, Organic Reactions, 1992, Vol.42, 335-656 and Progress in the Mitsunobu Reaction, D.L.Hughes, Organic Preparations and Procedures International, 1996, Vol.28,127-164.
Compounds of the formula (H) wherein Y is hydroxy may be obtained as described in the references cited herein (particularly in the section proceeding the discussion of protecting

groups), for example, by reacting a compound ef the formula (VI) with a compound of formula (VII):

wherein R21 is (l-6C)alkyl or benzyl and R22 is (l-4C)aIkyl or -S(0)„(l-4C)alkyl where n is 0, 1 or 2. Preferably R22 is (l-4C)alkyI.
In particular, compounds of the formula (IT), (VI) and (VII) may be prepared by the skilled man, for example as described in International Patent Application Publication Nos. WO95/07271, W097/27188, WO 97/30995, WO 98/01446 and WO 98/01446, the contents of which are hereby incorporated by reference, and by analogous processes.
If not commercially available, compounds of the formula (IE) may be prepared by procedures which are selected from standard chemical techniques, techniques which are analogous to the synthesis of known, structurally similar compounds, or techniques which are analogous to the procedures described in the Examples. For example, standard chemical techniques are as described in Houben Weyl, Methoden der Organische Chemie, E8a, Pt.I (1993), 45-225, B.J.Wakefield.
(b)( ii) Reactions (b)(ii) are performed conveniently in the presence of a suitable base such as, for example, an alkali or alkaline earth metal carbonate, alkoxide or hydroxide, for example sodium carbonate or potassium carbonate, or, for example, an organic amine base such as, for example, pyridine, 2,6-lutidine, collidine, 4-dimethylarninopyridine, Memylamine, morpholine or diazabicyclo-[5.4.0]undec-7-ene, the reaction is also preferably carried out in a suitable inert solvent or diluent, for example methylene chloride, acetonitrile, tetrahydrofuran,

1,2-dimethoxyethane, N N-dmiethylfomamLde, N,N-dtrnethylacetamide, N-methylpyrrolidin-2-one or dhnethylsulfoxide at and at a temperature in the range 25-60°C.
When Y is chloro, the compound of the formula (II) may be formed by reacting a compound of the formula (11) wherein Y is hydroxy (hydroxy compound) with a chlorinating agent. For example, by reacting the hydroxy compound with thionyl chloride, in a temperature range of ambient temperature to reflux, optionally in a chlorinated solvent such as dichloromethane or by reacting the hydroxy compound with carbon tetrachloride/triphenyl phosphine in dichloromethane, in a temperature range of 0°C to ambient temperature. A compound of the formula (II) wherein Y is chloro or iodo may also be prepared from a compound of the formula (II) wherein Y is mesylate or tosylate, by reacting the latter compound with lithium chloride or hthium iodide and crown ether, in a suitable organic solvent such as THF, in a temperature range of ambient temperature to reflux
When Y is (l-4C)alkanesulfonyloxy or tosylate the compound (H) may be prepared by reacting the hydroxy compound with (l-4C)alkanesulfonyl chloride or tosyl chloride in the presence of a mild base such as triemylamine or pyridine.
When Y is a phosphoryl ester (such as Ph02-P(0)-0-) or Pb2-P(0)-0- the compound (II) may be prepared from the hydroxy compound under standard conditions. (c) Reaction (c) is performed under conditions analogous to those described in the following references which disclose how suitable and analogous starting materials may be obtained.
Reaction (c) is especially suitable for compounds in which HET is an electron deficient heteroaryl (such as, for example, thiadiazole or triazine).
Compounds of the formula Q-Z wherein Z is an isocyanate may be prepared by the skilled chemist, for example by analogous processes to those described in Walter A. Gregory et al in J. Med. Chem. 1990, 33,2569-2578 and Chung-Ho Park et al in J. Med. Chem. 1992, 35,1156-1165. Compounds of the formula Q-Z wherein Z is a urethane may be prepared by the skilled chemist, for example by analogous processes to those described in International Patent Application Publication Nos. WO 97/30995 and WO 97/37980.,
A similar reaction to reaction (c) may be performed in which Q-Z wherein Z is a amine group is reacted with the epoxide (optionally in the presence of an organic base), and the product is reacted with, for example, phosgene to form the oxazolidinone ring. Such

reactions and the preparation of starting materials in within the skill of the ordinary chemist with reference to the above-cited documents disclosing analogous reactions and preparations.
Epoxides of the formula (V) may be prepared from the corresponding compound of formula (VIH):

Certain such epoxide and alkene intennediates are novel and are provided as a further feature of the invention. Asymmetric epoxidation may be used to give the desired optical isomer.
(d) The cycloaddition reaction to form 1,2,3 triazoles from the corresponding azide is performed under conventional conditions.
Compounds of the formula (II) wherein Y is azide may be obtained as described in the references cited herein (particularly in the section proceeding the discussion of protecting groups), for example from the corresponding compounds in which Y is hydroxy or mesylate. The removal of any protecting groups, the formation of apharmaceutically-acceptable salt and/or the formation of an in vivo hydrolysable ester are within the skill of an ordinary organic chemist using standard techniques. Furthermore, details on the these steps, for example the preparation of in-vivo hydrolysable ester prodrugs has been provided in the section above on such esters, and in certain of the following non-limiting Examples.
When an optically active form of a compound of the formula (T) is required, it may be obtained by carrying out one of the above procedures using an optically active starting material (formed, for example, by asymmetric induction of a suitable reaction step), or by resolution of a racemic form of the compound or intermediate using a standard procedure, or by chromatographic separation of diastereoisomers (when produced). Enzymatic techniques may also be useful for the preparation of optically active compounds and/or intermediates. Similarly, when a pure regioisomer of a compound of the formula (I) is required, it may be obtained by carrying out one of the above procedures using a pure regioisomer as a starting material, or by resolution of a mixture of the regioisomers or intermediates using a. standard procedure.

According to a further feature of the invention there is provided a compound of the formula (I), or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof for use in a method of treatment of the human or animal body by therapy.
According to a further feature of the present invention there is provided a method for producing an antibacterial effect in a warm blooded animal, such as man, in need of such treatment, which comprises administering to said animal an effective amount of a compound of the present invention, or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof.
The invention also provides a compound of the formula (I), or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof, for use as a medicament; and the use of a compound of the formula (I) of the present invention, or a pharmaceutically-acceptable salt, or in-vivo hydrolysable ester thereof, in the manufacture of a medicament for use in the production of an antibacterial effect in a warm blooded animal, such as man.
In order to use a compound of the formula (I), an in-vivo hydrolysable ester or a pharmaceutically-acceptable salt thereof, including a pharmaceutically-acceptable salt of an in-vivo hydrolysable ester, (hereinafter in this section relating to pharmaceutical composition "a compound of this invention") for the therapeutic (including prophylactic) treatment of mammals including humans, in particular in treating infection, it is normally formulated in accordance with standard pharmaceutical practice as a pharmaceutical composition. Therefore in another aspect the present invention provides a pharmaceutical composition which comprises a compound of the formula (I), an in-vivo hydrolysable ester or a pharmaceutically-acceptable salt thereof, including a pharmaceutically-acceptable salt of an in-vivo hydrolysable ester, and a pharmaceutically-acceptable diluent or carrier.
The pharmaceutical compositions of this invention may be administered in standard manner for the disease condition that it is desired to treat, for example by oral, rectal or parenteral adrninistration. For these purposes the compounds of this invention may be formulated by means known in the art into the form of, for example, tablets, capsules, aqueous or oily solutions or suspensions, (lipid) emulsions, dispersible powders, suppositories, ointments, creams, aerosols (or sprays), drops and sterile injectable aqueous or oily solutions or suspensions.

In addition to the compounds of the present invention the pharmaceutical compositio of this invention may also contain or be co-administered (simultaneously, sequentially or separately) with one or more known drugs selected from other clinically useful antibacterial agents (for example, B-lactams or aminoglycosides) and/or other anti-infective agents (for
i
example, an antifungal triazole or amphotericin). These may include carbapenems, for example meropenem or imipenem, to broaden the therapeutic effectiveness. Compounds of this invention may also contain or be co-administered with bactericidal/permeability-increasing protein (BPI) products or efflux pump inhibitors to improve activity against gram negative bacteria and bacteria resistant to antimicrobial agents.
A suitable pharmaceutical composition of this invention is one suitable for oral administration in unit dosage form, for example a tablet or capsule which contains between lmg and lg of a compound of this invention, preferably between lOOmg and lg of a compound. Especially preferred is a tablet or capsule which contains between 50mg and 800mg of a compound of this invention, particularly in the range lOOmg to 500mg.
In another aspect a pharmaceutical composition of the invention is one suitable for intravenous, subcutaneous or intramuscular injection, for example an injection which contam between 0.1% w/v and 50% w/v (between lmg/ml and 500mg/ml) of a compound of this invention.
Each patient may receive, for example, a daily intravenous, subcutaneous or
intramuscular dose of 0.5 mgkg-1 to 20 mgkg-1 of a compound of this invention, the composition being administered 1 to 4 times per day. In another embodiment a daily dose of i
mgkg-1 to 20 mgkg-1 of a compound of this invention is administered. The intravenous, subcutaneous and intramuscular dose may be given by means of a bolus injection. Alternatively the intravenous dose may be given by continuous infusion over a period of time, Alternatively each patient may receive a daily oral dose which may be approximately equivalent to the daily parenteral dose, the composition being administered 1 to 4 times per day.
A pharmaceutical composition to be dosed intravenously may contain advantageously (for example to enhance stability) a suitable bactericide, antioxidant or reducing agent, or a suitable sequestering agent.

In the above other, pharmaceutical composition, process, method, use and medicament manufacture features, the alternative and preferred embodiments of the compounds of the invention described herein also apply.
Antibacterial Activity:
The pharmaceutically-acceptable compounds of the present invention are useful antibacterial agents having a good spectrum of activity in vitro against standard Gram-positive organisms, which are used to screen for activity against pathogenic bacteria. Notably, the pharmaceutically-acceptable compounds of the present invention show activity against enterococci, pneumococci and methicillin resistant strains of S.aureus and coagulase negative staphylococci, together with haemophilus and moraxella strains. The antibacterial spectrum and potency of a particular compound may be determined in a standard test system.
The (antibacterial) properties of the compounds of the invention may also be demonstrated and assessed in-vivo in conventional tests, for example by oral and/or intravenous dosing of a compound to a warm-blooded mammal using standard techniques.
The following results were obtained on a standard in-vitro test system. The activity is described in terms of the minimum inhibitory concentration (MIC) determined by the agar-dilution technique with an inoculum size of 104 CFU/spot. Typically, compounds are active in the range 0.01 to 256 |xg/ml.
Staphylococci were tested on agar, using an inoculum of 104 CFU/spot and an
incubation temperature of 37°C for 24 hours - standard test conditions for the expression of methicillin resistance.
Streptococci and enterococci were tested on agar supplemented with 5% defibrinatec
horse blood, an inoculum of 10^ CFU/spot and an incubation temperature of 37°C in an atmosphere of 5% carbon dioxide for 48 hours - blood is required for the growth of some of the test organisms. Fastidious Gram negative organisms were tested in Mueller-Hinton brotli, supplemented with hemin and NAD, grown aerobically for 24 hours at 37°C, and with an innoculum of 5x104 CFU/well.
For example, the following results were obtained for the compound of Example 44a:

MICQig/mj)
0.125
0.25
0.25
0.06 0.13
Organism Staphylococcus aureus:
, Oxford
Novb. Res
MRQR Coagulase Negative Staphylococci
MS
MR
0.25
0.25
0.25
2
2
Streptococcus pyogenes
C203 Enterococcus faecalis Bacillus subtilis
Haemophilus influenzae ARC446
Moraxella catarrhalis ARC445
Novb. Res - Novobiocin resistant MRQR - methicillin and quinolone resistant MR = methicillin resistant MS = methicillin sensitive
Certain intermediates and/or Reference Examples described hereinafter within the scope of the invention may also possess useful activity, and are provided as a further feature of the invention.
The invention is now illustrated but not limited by the following Examples in which unless otherwise stated :-
(i) evaporations were carried out by rotary evaporation in vacuo and work-up procedures were carried out after removal of residual solids by filtration;
(ii) operations were carried out at ambient temperature, that is typically in the range 18-26°C and in air unless otherwise stated, or unless the skilled person would otherwise work under an inert atmosphere; (iii) column chromatography (fay the flash procedure) was used to purify compounds and

was performed on Merck Kieselgel silica (Art. 9385) unless otherwise stated; (iv) yields are given for illustration only and are not necessarily the maximum attainable; (v) the structure of the end-products of the formula (I) were generally confirmed by NMR and mass spectral techniques [proton magnetic resonance spectra were generally determined in DMSO-d6 unless otherwise stated using a Varian Gemini 2000 spectrometer operating at a field strength of 300 MHz, or a Bruker AM250 spectrometer operating at a field strength of 250 MHz; chemical shifts are reported in parts per million downfield from tetramethysilane as an internal standard (5 scale) and peak multiplicities are shown thus: s, singlet; d, doublet; AB or dd, doublet of doublets; dt, doublet of triplets; dm, doublet of multiplets; t, triplet, m, multiplet; br, broad; fast-atom bombardment (FAB) mass spectral data were generally obtained using a Platform spectrometer (supplied by Micromass) run in electrospray and, where appropriate, either positive ion data or negative ion data were collected]; (vi) intermediates were not generally fully characterised and purity was in general assessed by thin layer chromatographic, infra-red (IR), mass spectral (MS) or NMR analysis; and (vii) in which the following abbreviations may be used :-
® is a Trademark; DMF is N,N-dimeraylformamide; DMA is N,N-dimethylacetamide; TLC is thin layer chromatography; HPLC is high pressure liquid chromatography; MPLC is medium pressure liquid chromatography; DMSO is dimethylsulfoxide; CDC13 is deuterated chloroform; MS is mass spectroscopy; ESP is electrospray; EI is electron impact; CI is chemical ionisation; THF is tetrahydrofuran; TFA is trifluoroacetic acid; NMP is N-methylpyrrolidone; HOBT is 1-hydroxy-benzotriazole; EtOAc is ethyl acetate; MeOH is methanol; phosphoryl is (HO)2-P(0)-0-; phdsphiryl is (HO)2-P~0-; EDC is l-(3-dimemylaminopropyl)-3-ethylcarbodiimide (hydrochloride); PTSA is para-toluenesulfonic acid, (viii) Temperatures are quoted as °C.
Sample 1: (5R)-3-(4-fl.4-DioYa-8-a7aspiro[4.5ldec-8-vn-3-flaornphenvn-5-f1.2.3-triazol-lrylmethyl)oxazolJdin-2-one
(5J?)-3-(4-(ls4-Dioxa-8-azaspho[4,5]decan-8-yl)-3-fluorophenyl)-5-azidomemyloxazolidin-2-one (2.44 g, 6.5 mM) was dissolved in dioxane (50 ml), treated with nofbornadiene (2,98 g, 32.3 mM) and heated under reflux for 20 hours. After removal of the solvent, the residue was

dissolved in dichloromethane (350 ml) washed with water (3 x 200 ml), and dried over magnesium sulfate. After filtration and evaporation the residue was purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 2.5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (1.5 g). MS (ESP): 404 (MET) for C19H22FN5O4
NMR fCDCl,) 8: 1.79 (t,4H); 3.04 (t,4H); 3.80 (dd, 1H); 3.92 (s,4H); 4.04 (t, 1H); 4.70 (m, 2H); 4.96 (m, 1H); 6.85 (overlapping m, 2H); 7.20 (t, 1H); 7.66 (d, 1H); 7.71 (d, 1H).
The intermediates for this compound were prepared as follows (see also WO 95-25106 - Ex 3).
4-(1.4-Dioxa-8-azaspiro[4.5]dec-8-yl)-3-fluoronitrobenzene
3,4-DifJuoronitrobenzene (15.53 g, 0.098 M) was dissolved in acetonitrile (150 ml), and
treated with -N,N-diisopropylethylamine (31.5 g, 0.244 M) and l,4-dioxa-8-aza-
spiro[4,5]decane (15.36 g, 0.107 M). The mixture was stirred and heated to reflux for 18
hours. After cooling, product precipitated as a yellow solid, and was filtered off (16.1 g);
further product could be obtained by concentrating the residues (8.43 g).
MS (ESPY. 283 (MIT) for CI3H15FN204
NMRfCDCl,) 8: 1.86 (t,4H); 3.41 (t,4H); 4.00 (s,4H); 6.91 (t, 1H); 7.89(dd,lH); 7.96
(dd, 1H).
5- Amino-2-(l .4-dioxa-8-azaspiro[4.5]dec-8-yl)fluorobenzene
4-(l,4-Dioxa-8-azaspiro[4,5]dec-8-yl)-3-fluoronitrobenzene (24.48 g, 0.087 M) was dissolved in ethyl acetate (500 ml) treated with palladium catalyst (10% on carbon, 5 g) and hydrogenated at atmospheric pressure until the theoretical uptake of gas. After filtration through celite and evaporation, the required product was obtained as a pink solid of sufficient quality for use without purification (19.3 g). MS (ESP): 253 (MET) for C13HI7FN202
NMRfDMSO-d£) 8: 1.69 (t,4H); 2.84 (t,4H); 3.86 (s, 4H); 4.91 (s,2H); 6.28 (m,2H); 6.75 (t, 1H).

5-EthoxvcarbonvIammo-2-CL4-dioy:a-8-azaRpiro[4.5]dec-8-vnf1norobenzene 5-Amino-2-(l,4-dioxa-8'azaspiro[4,5]dec-8-yl)£luorobenzene (19.26 g, 0.076 M), was dissolved in dry pyridine (75 ml) and cooled under nitrogen with stirring to 0°. Ethyl chloroformate (9.08, 0.084 M) was added dropwise, and the mixture stirred 30 minutes at the same temperature. Ice-water (300 ml) was added, and stirring continued for 1 hour. The resulting precipitate was collected, washed thoroughly with water, and dried, to give the desired product of sufficient quality for use without purification (20.5 g). MSJCESE): 325 (MH+) for C16H2lFN204
NMRfDMSO-d^ 8: 1.21 (t,3H); 1.71 (t,4H); 2.96 (t, 4H); 3.88 (s,4H); 4.09 (q,2H); 6.95 (t, 1H); 7.09 (dd, 1H); 7.27 (dd, 1H); 9.54 (s, 1H).
(5/;)-3-f4-fl.4-Dioxa-8-azaspko[4.5]dec-8-vlV3-fluorophenvlV5-hydroxvrnethv1oyazolidin-2-
one
5-Emoxycarbonylamino-2-(l,4-dioxa-8-azaspiro[4,5]dec-8-yl)fluorobenzene (22.9 g, 0.071
M) was dissolved in dry tetrahydrofuran (250 ml) under nitrogen, cooled to -70°, and treated
dropwise over 30 minutes with a solution of lithium f-butoxide (1M in tetrahydrofuran, 77.6
ml), keeping the temperature below -70°. After stirring for 5 minutes, (i?)-glycidylbutyrate
(11.19 g, 0.077 M) was added, and stirring continued at -65° for 1 hour, before allowing the
temperature to rise to ambient over 16 hours. The precipitate was collected and washed with
tetrahydrofuran to give the desired product (17.8 g).
MS fESPI: 353 (MET) for C17H21FN,05
NMRtoMSO-d^ 8: 1.83 (t, 4H); 3.09 (t, 4H); 3.69 (dd, 1H); 3.82 (dd} 1H); 3.88 (dd,
1H); 3.96 (s, 4H); 4.07 (t, 1H); 4.72 (m, 1H); 4.92 (s, 1H); 7.05 (t, 1H); 7.15 (dd, 1H);
7.46 (dd, 1H).
r5ffV3-r4-ri.4-Dioxa-8-azaspiro[4.5]dec-8-v1)-3-f1iioropheTiylV5-Tnethanesulfonyloxvmethvl-r)Yazolidin-2-one
[5i2)-3-(4-(l,4-Dioxa-8-azaspko[4,5]dec-8-yl)-3-iluorophenyl)-5-hydroxymethyloxazolidin-2-ane (4.024 g, 11.43 mM) was dissolved in dichloromethane (200 ml), and treated with [riethylamine (1.45 g, 14.4 mM), then cooled under nitrogen to 0°. Methanesulfonyl chloride '1.32 g, 11.5 mM) was added dropwise, and the mixture stirred 18 hours allowing the

temperature to rise to ambient. The mixture was washed with water (3 x 75 ml), concentrated, and purified by chromatography on a 90 g silica Biotage column, eluting with 1% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (3.09 g). ! MaiESE):.431(MH+)for C18H23FN207S NMR (DMSO-d) 5: 1.82 (t, 4H); 3.03 (s, 3H); 3.08 (t, 4H); 3.84 (dd, 1H); 3.92 (s, 4H); 4.04 (t, 1H); 4.33 (dd, 1H); 4.43 (dd, 1H); 4.84 (m, 1H); 6.91 (t, 1H); 7.02 (dd, 1H); 7.34 (dd, 1H).
(5R)-3-(4-(l14-Dioxa-8-azaspiro[4.5]dec-8-yl)-3-fluorophenyl)-5-azidomethyloxazolidm-2-
PJQS
(5R)-3-(4-(l,4-Dioxa-8-azaspiro[4,5Jdec-8-yl)-3-fluorophenyl)-5-methanesulfonyIoxymethyl-
oxazolidin-2-one (3.03 g, 7.04 mM) was dissolved in N,N-dimemylformamide (50 ml), treated
with sodium azide (732 mg, 11.3 mM), and heated with stirring at 50° for 4 hours. After
cooling the mixture was diluted with water (250 ml), and extracted into ethyl acetate (3 x 100
ml). The combined organics were dried (magnesium sulfate), and evaporated to give product
(2.44 g), of sufficient quality for use without purification.
MS (ESP): 378 (MH4) for C]7H2()FN504
NMR (CDCl3) 6: 1.73 (t,4H); 3.02 (t,4H); 3.66 (dd, 1H); 3.74 (m, 2H); 3.91 (s,4H); 4.11
(t, IB); 4.86 (m, 1H); 7.09 (t, 1H); 7.17 (dd, 1H); 7.48 (dd, 1H).
Example 2: (5JgV3-r4-f4-Oxopiperidin-l-vn-3-flnorophenyn-5-(1.2.3-triazoM-yImethyI)oxazolidin-2-one
(5i?)-3-(4-(l ,4-Dioxa-8-azaspiro[4,5]dec-8-yl)-3-fluorophenyl)-5-(l ,2,3-triazol-l -ylmethyl)oxazolidin-2-one (1.47 g, 3.65 mM) was dissolved in amixture of glacial acetic acid (30 ml) and water (30 ml), and heated at 50° for 18 hours. Solvent was evaporated, the residue azeotroped with toluene (50 ml), then partitioned between ethyl acetate (150 ml) and water (100 ml). The organic layer was washed with saturated aqueous sodium bicarbonate solution (2 x 100 ml), water (100 ml), dried (magnesium sulfate) and evaporated to give product (894 mg), of sufficient quality for use without purification. MS (ESP): 360 (MET) for C17H18FN503

NMR(CDC1^ 8: 2.53 (t, 4H); 3.29 (t, 4H); 3.84 (dd, IH); 4.06 (t, IH); 4.71 (d, 2H); 4.97 (m, IH); 6.90 (overlapping m, 2H); 7.24 (dd, IH); 7.67 (d, IH); 7.72 (d, IH).
Example 3: f5J?V3-f4-f4-Aminopiperidui.-1 -vn-3-fluorophenvr>-5-fL2.3-triazo1-1 -ylmeth vnoxazolidin-l-nTi R
(5fl)-3-(4-(4-Oxopiperidin-l -yl)-3-fluorophenyl)-5-(l ,2,3-triazol-l -yl) methyl)oxazolidin-2-
one (838 mg, 2.33 mM) was dissolved in methanol (25 ml), treated with ammonium acetate
(1.8 g, 23.3 mM) and sodium cyanoborohydride (1.03 g, 16.3 mM) and refluxed 16 hours.
The mixture was neutralised with 1 N hydrochloric acid, water (125 ml) added, extracted with
dichloromethane (5 x 75 ml), and dried (magnesium sulfate). Evaporation gave the desired
product (686 mg).
MS (ESP): 361 (MH+) for C17H21FN602
NMR rDMSO-d6) 5: 1.43 (m,2H); 1.86(dd,2H); 2.71(tm,4H); 3,29 (m, IH); 3.90 (dd,
IH); 4.25 (t, IH); 4.87 (d, 2H); 5.15 (m, IH); 7.08 (t, IH); 7.12 (dd, IH); 7.42 (dd, IH);
7.81 (d, IH); 8.21 (d, IH); NH2 exchanged, not seen.
Example 4: f5JgV3-(;4-r4-MethaTiesulfonamidopiperidiii-l-vn-3-flnorophenylV5-ri.2,3" triazoI-l-yImethyI)oxazoIidin-2-one
(5if)-3-(4-(4-Aimnopiperidm-l-yl)-3-iluorophenyl)-5-(l,2,3-tria2ol-l-yl)memyl)oxa^^ 2-one (175 mg, 0.49 mM) in dichloromethane (10 ml) was treated with triemylamine (78 mg, 0.78 mM) and methanesulfonyl chloride (67 mg, 0.58 mM) and the mixture stirred for 18 hours at ambient temperature under nitrogen. The niixture was filtered, and solution purified directly by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 2.5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (19 mg). MSJESE): 439(MH+)forC18H23FN604S
NMR fDMSO-d^ 8: 1.66 (m,2H); 1.98(dd,2H); 2.76(tm,4H); 3.00 (s, 3H); 3.89 (dd, IH); 4.12 (dd, IH); 4.25 (t, IH); 4.87 (d, 2H); 5.17 (m, IH); 7.08 (t, IH); 7.14 (d, IH); 7.19 (dd, IH); 7.42 (dd, IH); 7.81 (d, IH); 8.21 (d, IH).

Example 5: (5R)-3-r4-r4-MethoxycarbonvIaminopiperfdin-l-vn-3-fluorophenvn-f>-ri.2.3-triazo1-l-vlmethynoxazo1idin-2-one
(5J2)-3-(4-(4-Aminopiperidin1-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-yl)methyl)oxazolidin
2-one (151 mg, 0.42 mM) in dichloromethane (20 ml) was cooled to 0° and treated with 5%
sodium bicarbonate solution (4 ml). The resulting suspension was stirred vigorously, methyl
chloroformate (245 mg, 2.6 mM) added, and stirring continued for 3 hours at ambient
temperature. The dichloromethane was removed by evaporation, ethyl acetate (15 ml) added,
and the organic layer was separated, washed with 2% sodium dihydrogen phosphate (2x15
ml), brine (15 ml), and dried (magnesium sulfate), to give the desired product (170 mg).
MSiESE): 419(MHf)forC19H23FN604
NMR (DMSO-d6) 8: 1.53(qm,2H); 1.82(dd,2H); 2.68 (t,2H); 3.24 (m,2H); 3.39 (m,
IH); 3.52 (s, 3H); 3.83 (dd, IH); 4.18 (t, IH); 4.83 (d, 2H); 5.09 (m, IH); 7.02 (t, IH);
7.06(dd,lH); 7.15 (d, IH); 7.36(dd,lH); 7.74 (d, IH); 8.14 (d, IH).
Example 6: (5JgV3-(4-(4-Methylaminopiperidm-l-yl)->3-flnoropheny][)-5-(1.2.3-triazoI-l" ylmethyl)oxazolidm-2~one
(5i2)-3-(4-(4-Oxopiperidm-l-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-ylmemyl)oxazolidm-2-(250 mg, 0.70 mM) was dissolved in a mixture of anhydrous tetrahydrofuran (5 ml) and dichloromethane (5 ml) under nitrogen. Acetic acid (1 drop), methylamine (33% solution in methanol, 31uJL, 0.77 mM) and sodium acetoxyborohydride (222 mg, 1.05 mM) were added, and the mixture stirred at ambient temperature for 3 hours. The mixture was diluted with water (15 ml) and dichloromethane (15 ml), and the pH adjusted to 9 by addition of triemylamine. The organic phase was separated, washed with water (2 x15 ml), brine (15 ml), and dried (magnesium sulfate). Evaporation gave the desired product (145 mg). MS (ESP): 375(MH+)forC18H23FN602
NMRflDMSO-d^ 6: 1.45 (m, 2H); 1.95 (dd, 2H); 2.36 (s, 3H); 2.48 (dd, 2H); 2.71 (t, 2H); 3.91 (dd, IH); 4.25 (t, IH); 4.87 (d, 2H); 5.16 (m, IH); 7.10 (overlapping m, 2H); 7.45 (dd, IH); 7.81 (d, IH); 8.22 (d, IH); NH exchanged, CH-—N under H20, neither seen.
Example 7: (5R)-3-(4-(4-Ar-Methy1-niethaDesa1fonamidopiperidiii-1 -v1V3-fluorophenvlV 5-(1.2.3-triazoI-l-ylmethyI)oxazolidm-2-one

(5R)-3-(4-(4-Methylammopiperidm-lyi)-3fluorophenyl)-5-(1,2,3-triazol-1yl)methyl)-
oxazolidin-2-one (200 mg, 0.53 mM, Example 6), was treated essentially as Example 4 to

give the title product after chromatography (53 mg).

MS (ESP): 453 (MH+) for C^FNAS

NMR(DMSOd6) 8: 1.79 (d,2H); 2.00 (ddd, 2H); 2.74 (t,2H); 2.84 (s,3H); 2.87 (s, 3H);

3.44 (d, 2H); 3.87 (m, IH); 3.89 (dd, IH); 4.12 (t, IH); 4.77 (d, 2H); 5.04 (m, IH); 6.89 (t,

IH); 6.95 (dd, IH); 7.28 (dd, IH); 7.74 (d, IH); 7.79 (d, IH).

Example 8: (5R))-3-r4-r4-iV-MethyI-methoxycarbonyIaminopiperidm-l-yn-3-
fhiorophen vIV5-(l .2.3-triazol-l -vlmeth vnoxazoIidin-2-one

(5J2)-3-(4-(4-Methylarnmopiperidin-l-yl)-3-fl^^

oxazolidin-2-one (200 mg, 0.53 mM, Example 6), was treated essentially as Example 4,

except for the substitution of methyl chloroformate for methanesulfonyl chloride, to give the

title product after chromatography (131 mg).

MS(ESP): 433 (MH4) for CjoH^FNA

NMRfDMSO-d^ 5: 1.62 (d,2H); 1.82 (ddd, 2H); 2.69 (t,2H); 2.74 (s,3H); 3.32 (d,2H);

3.59 (s, 3H); 3.83 (dd, IH); 3.92 (m, IH); 4.18 (t, IH); 4.81 (d, 2H); 5.10 (m, IH); 7.03 (t,

IH); 7.08 (dd, IH); 7.37 (dd, IH); 7.73 (d, IH); 8.13 (d, IH).

Example 9: (5igV3 phenyl)-5-(1.23-triazol-l-ylmethyl)oxazolidin"2-one

(5i2)-3-(4-(4-Memylanimopiperidm-l-yl)-3-fl^^

oxazolidin-2-one (350 mg, 0.94 mM, Example 6), was treated essentially as Example 4,

except for the substitution of acetoxyacetyl chloride for methanesulfonyl chloride, to give the

title product after chromatography (207 mg).

MS (ESP): 475 (MH4) for C22H27FN605

NMRfDMSO-d.) 8: 1.75 (d,2H); 1.87(dd,2H); 2.07 (s,3H); 2.70 (t,2H); 2.74 (s,3H);

3.36 (d, 2H); 3.62 (m, IH); 3.83 (dd, IH); 4.18 (t, IH); 4.53 (s, 2H); 4.82 (d, 2H); 5.11 (m,
IH); 7.10 (overlapping m,2H); 7.49 (dd, IH); 7.76 (d, IH); 8.16 (d, IH).

Example 10: (5R) )-3-(4-4-N-MethyNr2-hydro^acetvnami>npfperidm-1-ylV3-fluQrophenvlV5-fl.2.3-triazol-1-vlmethvl1>oxazolidin-2-one
(5i?)-3-(4-(4-A^-Methyl-(2-acetoxyacetyl)ammopiperidin 1-yl)-3-fluorophenyl)-5-(l^ triazol-l-ylmethyl)oxazolidin-2-one (186 mg, 0.39 mM) was dissolved in methanol (20 ml), i treated with potassium carbonate (0.3 g, 2.1 mM) and stirred at ambient temperature for 30 minutes, After removal of the solvent the residue was purified by chromatography on a 5 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (30 mg). MS (ESP): 433 (MIT) for C20H25FN6O4
NMRXDMSQdi^ 8: 1.73 (d, 2H); 1.93 (ddd, 2H); 2.74 (t, 2H); 2.79 (s, 3H); 3.45 (d, 2H); 3.68 (s, IH); 3.89 (dd, IH); 4.11 (t, IH); 4.16 (s,2H); 4.58 (m, IH); 4.79 (d,2H); 5.04 (m, IH); 6.91 (t, IH); 6.95 (dd, IH); 7.29 (dd, IH); 7.73 (d, IH); 7.79 (d, IH).
Example 11: f5JgV3-r4-r4-(2^-2.3-DihvdroxvpropioiiyI)piperazin-l -yn-3-flttorophenvlV 5-( 1.2.3-triazol-1 -vImefliyl)oxazoIidih-2-one
(5i?)-3 NMR fDMSO-d^ 5: 2.91 (brm, 4H); 3.45 (m, IH); 3.51 (m, IH); 3.63 (brm, 4H); 3.82 (dd, IH); 4.18 (t, IH); 4.34 (dd, IH); 4.66 (t, IH); 4.80 (d, 2H); 4.91 (d, IH); 5.11 (m, IH); 7.04 (t5 IH); 7.11 (dd, IH); 7.39 (dd, IH); 7.74 (d, IH); 8.13 (d, IH).
The intermediates for this compound were prepared as follows:

I. '£>
£ifii,.. 4-r4-M^utoxvcarbonylpiperazin-l-ylV3-f]uorophenyl)-5-rL2.3-tria7ol-1-vlmethvnoxazolidiTi-2-nr^R
(5i^)-3-(4-(4-^Butoxycarbonylpiperazin4-yl)-3"fluorophenyl)-5-azidomethyl)oxazolidill-2-
one (2.52 g, 6 rnM) and norbornadiene (4.2 g, 45.6 mM) were dissolved in dioxane (50 ml)
and heated under reflux for 6 hours. After evaporation of solvent, the residue was purified by
recrystallisation from isopropanol (50 ml) to give the desired product (2.29 g).
MS (ESP): 447(MH^forC21H27FN604
NMR (DMSO-d^ 8: 1.40 (s, 9H); 2.81 (t, 4H); 3.45 (t, 4H); 3.83 (dd, 1H); 4.18 (t, 1H);
4.79 (d,2H); 5.10 (m,lH); 7.06 (t, 1H); 7.11(dd, 1H); 7.38 (dd, 1H); 7.73 (d, 1H); 8.13
(d,lH).
(Intermediate oxazoHdinone described in Upjohn WO 93-23384)
r5flV3-(;4-(Tiperazin-l-viy3-fluoropheeny)-5-1,2,3-triazol-1-ylmethyl)oxazolidin-2 one
(5R)-3 -(4-(4-f-Butoxycarbonylpiperazin-1 -yl)-3-fiuorophenyl)-5-(l ,2,3 -triazol-1 -
ylmethyl)oxazolidin-2-one (2.0 g, 4.48 mM), was suspended in ethanol (20 ml), and treated
with a solution of hydrogen chloride in ethanol (3.8M, 15 ml). After stirring 18 hours at
ambient temperature, the solution was evaporated to dryness, and the residue recrystallised
from ethanol and diethyl ether, with charcoal treatment to give the product as its
dihydrochloride salt (0.72 g).
kl&XESE): 347 (MIT) for C16H19FN602
IVTicroanalvsis: Found, C 46.2; H5.1; N 18.8%. G16H19FN602-2HC1 requires C 45.8; H5.0;
Nf20.0%
r5^)-3-(4-f4-r(^S)-2.2-Dimemvl-1.3-dioxolane-4-carbonvnpiperazin-1-yn-3-flunrophenyl)-5-[] .2.3 -triazol-1 -vlmethvDoxazoliri jt|-2-nne
Fhe Uthium salt of (4S>2,2-dimemyl-l,3-dioxolan-4-carboxylic acid (342 mg, 2.25 mM) in iichloromethane (10 ml) under nitrogen was cooled with stirring to 0°, treated with thionyl chloride (321 mg, 2.7 mM), then stirred at the same temperature for 3 hours. After filtration, he residue was evaporated to dryness, and redissolved in dichloromethane (10 ml), then tdded to a stirred suspension of (Jif)-3-(4-piperazin-l-yl-3-fluorophenyl)-5-(l,2,3-triazoH-^lmethyl)oxazolidin-2-one dihydrochloride (630 mg, 1.5 mM) in dichloromethane (30 ml)

containing pyridine (370 rug, 4.9 mM) and triethylamine (500 mg, 4.9 mM). The mixture was stirred for 18 hours, allowing the temperature to rise to ambient. After dilution with dichloromethane (30 ml), the organic layer was separated, washed with water (3x30 ml), brine (50 ml), and dried (magnesium sulfate). The residue after evaporation was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (278 mg). MS (ESP): 475 (MH*) for C22H27FN605
NMRfDMSO-d^) 8: 1.32 (s,6H); 2.95 (br m, 4H); 3.63 (m,4H); 3.86 (dd, 1H); 4.08 (t, 1H); 4.21 (m, 2B); 4.83 (d, 2H); 4.89 (t, 1H); 5.12 (m, 1H); 7.07 (t, 1H); 7.12 (dd, 1H); 7.42 (dd, 1H); 7.77 (d, 1H); 8.17 (d, 1H).
Examples 12-16
(5R)-3-(4-(4-(2-Chloroaceryl)piperazin-l-yl)-3-fluorophenyl)-5-(ls2,3-triazol-l-5 ylmethyl)oxazolidin-2-one (422 mg, 1 mM) and the appropriate amine (3 mM) were dissolved in a mixture of dichloromethane (10 ml) and ethanol (1 ml) and stirred at ambient temperature for 18 hours. Solvent was evaporated and the residue purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with an appropriate increasing gradient of methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired i products.

Notes
1 MS (ESP^: 474(MH+)for C22H28FN704
NMR(DMSO-d6) 8: 2.40(br,4H); 2.90(br,2H); 2.96(br,2H); 3.19 (br,2H); 3.56 (br, 6H); 3.65 (br, 2H); 3.84 (dd, 1H); 4.20 (t, 1H); 4.83 (d, 2H); 5.12 (m, 1H); 7.06 (t, 1H); 7.11 (dd, 1H); 7.41 (dd, 1H); 7.75 (d, 1H); 8.17 (d, 1H).
2 Sample after chromatography dissolved in the minimum volume of ethanol,
treated with a solution of hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether
to precipitate the hydrochloride salt.
MS (ESP): 462(MH4)for C21 H28FN704
NMRflPMSO-d^ 5: 2.87 (d,3H); 2.99 (brm, 4H); 3.19 (brm, 1EQ; 3.28 (brm, 1H); 3.49 (br, 2H); 3.64 (br, 2H); 3.76 (t, 2H); 3.85 (dd, 1H); 4.18 (t, 1H); 4.34 (dd, 1H); 4.46 (dd, 1H); 4.81 (d, 2H); 5.11 (m, 1H); 7.04 (t, 1H); 7.13 (dd, 1H); 7.40 (dd, 1H); 7.74 (d, 1H); 8.16 (d, 1H); 9.58 (br, 1H); OH missing under solvent; +1H for HC1 salt
3 Little reaction in ethanol at ambient temperature; solvent replaced by
isopropanol (10 ml), and refluxed 18 hours before work up as above. Sample after
chromatography dissolved in the minimum volume of ethanol, treated with a solution of
hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether to precipitate the
hydrochloride salt.
MS (ESP): 489(MH+)forC22H29FNg04
NMR(DMSO-d^) 5: 1.83 (s, 3H); 2.97 (br, 6H); 3.33 (brm, 2H); 3.51 (br, 2H); 3.64 (br, 2H); 3.85 (dd, 1H); 4.10 (brt, 2H); 4.18 (t, 1H); 4.81 (d, 2H); 5.11 (m, 1H); 7.050 (t, 1H); 7.13 (dd, 1H); 7.41 (dd, 1H); 7.74 (d, 1H); 8.16 (d, 1H); 8.27 (brt, 1H); 9.07 (br, 2H); +1H for HC1 salt.
4 Sample after chromatography dissolved in the minimum volume of ethanol,
treated with a solution of hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether

' to precipitate the hydrochloride salt. MS (ESP): 476 (MET) for C22H30FN704
NMR (DMSO-d6) 8: 2.87 (d,3H); 2.99 (m,4H); 3.28 (s, 3H); 3.33 (m, IH); 3.42 (m
overlapped by solvent, ~1H); 3.52 (br, 2H); 3.69 (t overlapping br, 4H); 3.86 (dd, IH); 4.20
(t, IH); 4.33 (dd, IH); 4.43 (dd, IH); 4.84 (d, 2H); 5.13 (m, IH); 7.05 (t, IH); 7.13 (dd,
IH); 7.42 (dd, IH); 7.75 (d, IH); 8.18 (d, IH); 9.78 (br, IH); +1H for HC1 salt
5 Sample after chromatography dissolved in the minimum volume of ethanol,
treated with a solution of hydrogen chloride in ethanol (3.8M, 1 ml), then excess diethyl ether to precipitate the hydrochloride salt. MS CESP): 462(MH+)forC21H28FN704
NMRfDMSO-d^ 8: 2.72 (t, 2H); 2.93 (t, 4H); 3.25 (s, 3H); 3.39 (t, 2H); 3.52 (s, 2H); 3.54(br,2H); 3.63(br,2H); 3.84(dd,lH); 4.18 (t, IH); 4.80 (d,2H); 5.11 (m, Iff); 7.03 (t, IH); 7.12 (dd, IH); 7.41 (dd, IH); 7.76 (d, IH); 8.16 (d, IH); NH missing under solvent.
The intermediate for these compounds was prepared as follows:
(5^-3-r4-(4-pipera7in-l-ylV3-fluorophenvlV5-n ■2.3-triazoU -
ylmethvfloxa2olidm-2-one
(5jR)-3-(4-(Piperazm-l-yl)-3-iluorophenyl)-5-(1,2,3-triazol-1ylmethyl)oxazolidin-2one
dihydrochloride (4.19 g, 10 mM) was suspended in dry dichloromethane (100 ml) under
nitrogen and treated with triethylamine (3.03 g, 30 mM) to give a solution. After cooling to
4°, chloroacetyl chloride (1.14 g, 10 mM) was added and the mixture stirred for 15 minutes.
The volume was reduced to 20 ml, and the solution chromatographed on silica, eluting with
dichloromethane (30 ml). Relevant fractions were combined, washed with water (50 ml) and
dried (magnesium sulfate). Evaporation gave the desired product (2.86 g).
MS(ESP) - 423 (MIT) for C18H20ClFN6O3
NMR fDMSO-d^ S: 2.93 (br, 2H); 2.98(br,2H); 3.60(br,4H); 3.84(dd,lH); 4.18 (t,
IH); 4.41 (s, 2H); 4.81 (d, 2H); 5.11 (m, IH); 7.06 (t, IH); 7.13 (dd, IH); 7.42 (dd, IH);
7.76 (d,lH); 8.16 (d, IH).

Example 17: (5RV3-(4-((3R)-3-t-ButoxycarbonvnammopvrroIidin-l-yn-3-fluorn-phenyI)-5-(1.23-triazoM-yImethyfloxazolidin~2-one
(5i?)-3-(4-((3i?)-3-(^Butoxycarbonyl)arrmiopyrrolidin-l-yl)-3-fluorophenyl)-5-azidomethyl-oxazolidin-2-one (695 mg, 1.65 mM) was dissolved in dioxane (30 ml), treated with norbornadiene (760 mg, 8.25 mM) and heated under reflux for 6 hours. After removal of the solvent, the residue was dissolved in the minimum of dichloromethane and purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 2.5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (544 mg). MS (ESP): 447 (MH4) for C21H27FN604
NMRfCDCl^ 5: 1.44 (s, 9H); 1.86 (m, IH); 2.24 (m, IH); 3.22 (d, IH); 3.31 (t, IH); 3.52 (m, 2H); 3.84 (dd, IH); 4.04 (t, IH); 4.28 (br, IH); 4.74 (m, 3H); 5.01 (m, IH); 6.58 (t, IH); 6.87 (dd, IH); 7.18 (dd, IH); 7.73 (d, IH); 7.78 (d, IH).
The intermediates for this compound were prepared as follows:
3-Fluoro-4-((3R)-3-(t-butoxycarbonyl)aminopyrrohdin-l-yl)mtrobenzene 3,4-Difluoronitrobenzene (16.03 g, 0.101 M) was dissolved in acetonitrile (300 ml), and treated with JVyV-du^opropylemylarnine (32.63 g, 0.253 M) and (3i?)-3-(f-butoxycarbonyl)-aminopyrrolidine (20.65 g, 0.111 M). The mixture was stirred and heated to reflux for 18 hours. Solvent was evaporated, and the residue treated with ethyl acetate (300 ml) and water (200 ml). The organic layer was washed with water (150 ml), citric acid solution (10% in water, 2 x 150 ml), and dried (magnesium sulfate). Evaporation gave the desired product as a yellow solid (32.7 g), of sufficient quality for use without purification. MS (ESP): 326(MH+)forC15H20FN3O4
NMR (CDCl2) 5: 1.43 (s, 9H); 1.85 (m, IH); 2.25 (m, IH); 3.44 (dt, IH); 3.65 (overlapping m, 2H); 3.84 (dm, IH); 4.34 (br m, IH); 4.69 (br, IH); 6.53 (t, IH); 7.87 (dd, IH); 7.92 (dd, IH).
5-Amino-2-((3R)-3-(t-butoxycarbonvl)aminnpyrrolidm-l--yl)fluorobenzene 3-Fluoro-4
was dissolved in ethyl acetate (500 ml) treated with palladium catalyst (10% on carbon, 7.5 g) and hydrogenated at atmospheric pressure until the theoretical uptake of gas. After filtration through celite and evaporation, the required product was obtained as a red gum of sufficient quality for use without purification (29.85 g). MS (ESP): 296 (MH4) for C^PNA NMR rCDC12) 8: 1.44 (s, 9H)l 1-82 (m, 1H); 2.27 (m, 1H); 3.11 (m, 2H); 3.37 (m, 2H); 3.4^,2Hy, 4.27(bim,lHy, 482(br,lHy, 63S(dd,lKy, 6.44 (dd, VKy, 6.57 (t,lH).
5-Ethoxyc3rhnr>Y|arpiTin-9-((3R-3-(t-butoxycarbonynaminopvn-olidin4-vnf]uoroberi2e 5-Ammo-2-((3R)-3-^butoxycarbonyl)arnmopyrrohdin-l-yl)fluorobenzene (27.33 g, 0.093 M) was dissolved in dry pyridine (150 ml) and cooled under nitrogen with stirring to 0°. Ethyl chloroformate (11.01, 0.102 M) was added dropwise, and the mixture stirred 30 minutes at the same temperature. Ice-water (250 ml) was added, and stirring continued for 1 hour. The resulting precipitate was collected, washed thoroughly with water, and dried, to give the desired product of sufficient quality for use without purification (33.6 g). MS (ESP): 368 (MS") for C18H26FN304
NMRfDMSO-da) 5: 1.21 (t, 3H); 1.36 (s, 9H); 1.90 (m, 1H); 2.05 (m, 1H); 3.04 (m, 1H); 3.20 (m, 1H); 3.32 (m, 1H); 3.40 (m, 1H); 4.02 (br, 1H); 4.05 (q, 2H); 6.62 (t, 1H); 7.02 (d, 1H); 7.08 (d, 1H); 7.22 (d, 1H); 9.38 (br, 1H).
(5/?V3'r3-Fluoro-4-rf3igV3-r^butoxvcarbonvl)aminopyrrolidin4-yl)-5-hydroxymethyl-
oxazolidin-2-one
5-Emoxycarbonylammo-2-((3jR)-3-(t-butoxycarbon^
(33.6 g, 0.092 M) was dissolved in dry tetrahydrofuran (300 ml) under nitrogen, cooled to
-70°, and treated dropwise over 30 minutes with a solution of lithium /-butoxide (1M in
tetrahydrofuran, 100.7 ml), keeping the temperature below -65°. After stirring for 5 rninutes,
[R)-glycidylbutyrate (14.52 g, 0.101 M) was added, and stirring continued at -65° for 1 hour,
jefore allowing the temperature to rise to ambient over 16 hours. The mixture was treated
,vith methanol (50 ml), stirred at ambient temperature for 1 hour, and the precipitate collected
md washed well with tetrahydrofuran to give the desired product (21,8 g).
VIS fESP): 396 (MH*) for C,9H26FN305

3.35 (m, IH); 3.49 (m, 2H); 3.62 (m, IH); 3.73 (dd, IH); 3.98 (t, IH); 4.04 (m, IH); 4.63 (m, IH); 5.15 (t, IH); 6.70 (t, IH); 7.09 (dd overlapping br, 2H); 7.39 (dd, IH).
r5igV3-r4-rr3i?V3-(t-butoxvcarbonvDaminopyrrolidm-l-vlV3-fluoropheny1V5-
metaanesulfonyloxymethyloxazolidm-2-one
(5i?)-3-(4-((5i?)-3-^butoxycarbonyl)ammopyrrolidin^l-yl)-3-fluorophenyl)-5-
hydroxymethyloxazolidin-2-one (3.99 g, 10.1 mM) was suspended in dichloromethane (50
ml), and treated with Memylamine (1.53 g, 15.2 mM), then cooled under nitrogen to 0°.
Methanesulfonyl chloride (1.39 g, 12.12 mM) was added dropwise, and the mixture stirred 18
hours allowing the temperature to rise to ambient. Precipitated hydrochloride was filtered, the
filtrate washed with saturated sodium bicarbonate (75 ml) and water (3 x 75 ml),
concentrated, and purified by chromatography on a 90 g silica Biotage column, eluting with
dichloromethane. Relevant fractions were combined and evaporated to give desired product
(1.25g).
MS fESPV 474 (MEt) for C20H28FN3O7S
NMRfCDO,) 8: 1.37 (s,9H); 1.82 (m, IH); 2.17 (m, IH); 3.03 (s,3H); 3.17 (d, IH);
3.26 (t, IH); 3.48 (m, 2H); 3.82 (dd, IH); 4.03 (t, IH); 4.24 (br, IH); 4.33 (dd, IH); 4.41
(dd, IH); 4.72 (br, IH); 4.83 (m, IH); 6.57 (t, IH); 6.96 (dd, IH); 7.27 (dd, IH).
(5Jg)-3-(4-((3ig)-3-(/-butoxycarbonyl)aminopyrrolidin-1yl)-3-fiurophenyl)-5azidomethyl)-
oxazolidin-2-one
(5iJ)-3-(4-((3R)-3-(^butoxycarbonyl)ammopyrroUdin-l-yl)-3-fluorophenyl)-5-methane-
sulfonyloxymethyloxazohdin-2-one (1.25 g, 2.64 mM) was dissolved in AyV-dimethyl-
formamide (20 ml), treated with sodium azide (275 mg, 4.23 mM), and heated with stirring at
50° for 5 hours. After cooling the mixture was diluted with water (100 ml), and extracted into
ethyl acetate (3 x 75 ml). The combined organics were dried (magnesium sulfate), and
evaporated to give a yellow solid, whichl4:32 was recrystallised from isopropanol to give the
required product (715 mg).
MS CESV): All (MH*) for C19h25fn6o4

NMR(CDC1^ 5: 1.37 (s, 9H); 1.82 (m, IH); 2.17 (m, IH); 3.17 (d, IH); 3.25 (t, IH);

3.51 (dd overlapping m, 3H); 3.61 (dd, IH); 3.71 (dd, IH); 3.95 (t, IH); 4.25 (br, IH); 4.78

(m, 2H); 6.57 (t, IH); 6.98 (dd, IH); 7.28 (dd, IH).
Example 18: f5jRV3-r4-rr.?ffV3-AminopvrroIidin-l-yn-3-flnorophenvIV5-fl.2.3-triazo1-l-ylmethyI)oxazolidin-2-one
(5^)-3-(4-((3i?)-3"^Butoxycarbonyl)arm^opyiroUdm4-yl)-3-fluorophenyl)-5 NMRfDMSO-dJ 8: 2.03 (m, IH); 2.25 (m, IH); 3.25 (dd, IH); 3.41 (m, IH); 3.51 (m, 2H); 3.82 (overlapping m,2H); 4.17 (t, IH); 4.81 (d,2H); 5.08 (m, IH); 6.74 (t overlapped byH20,~lH); 7.05 (dd, IH); 7.32(dd,lH); 7.74 (d, IH); 8.15 (d, IH); 8.43 (br, ~2H).
Example 19: r5J?V3-r4-rr.?/?V3-MethoxycarhonylaminopvrroIidm-l-yIV3-fluorophenvlV 5-(1.2.3-triazol-l-yImethyI)oxazolidin-2-one
(5i?)-3-(4-((3i?)-3-AmmopyrroHdm-l-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-yhnethyl)oxazolidin-2-one hydrochloride (200 mg, 0.5 mM) in dichloromethane (20 ml) was cooled to 0° and treated with 5% sodium bicarbonate solution (5 ml). The resulting suspension was stirred vigorously, methyl chloroformate (245 mg, 2.6 mM) added, and stirring continued for 3 hours at ambient temperature. The organic layer was separated, washed with 2% sodium dihydrogen phosphate (2x10 ml), brine (10 ml), and dried (magnesium sulfate), to give the desired product (143 mg). MS (ESP): 405 (MH4) for C18H21FN604
NMR (DMSO-d£> 5: 1.82 (m, IH); 2.11 (m, IH); 3.13 (m, IH); 3.27 (dd, IH); 3.37 (dd, IH); 3.53 (s overlapping m, 4H); 3.81 (dd, IH); 4.09 (m, IH); 4.15 (t, IH); 4.80 (d, 2H); 5.08 (m, IH); 6.69 (t, IH); 7.01 (dd, IH); 7.28 (dd, IH); 7.42 (br, IH); 7.75 (d, IH); 8.13 (d, IH).

Example 20: r5/gV3^4-rf3RV3-rf4SV2.2-dimethvI-1.3-dioxolan-4-yImethoxy-
carbonylammo)pyrrolidin-l-yI)-3-fluorophenyIV5-ri.2.3-ti,iazoI-l-ylmethyI)oxazolidin-
2-one
(J29-3-(4-((3/0-3-Ainmopym)H^
oxazolidin-2-one hydrochloride (400 mg, 1.05 mM) was suspended in tetrahydroiuran (10 ml)
and treated with du^opropylethylarnine (176 mg, 1.36 mM) and (4S)-2,2-dimethyl-l,3-
dioxolan-4-ylmethyl 4-nitrophenyl carbonate (429 mg, 1.44 mM) dissolved in
dichloromethane (5 ml). The mixture was stirred vigorously at ambient temperature for 18
hours, with the addition of two further portions of dusopropylemylarnine (137 mg, 1.06 mM).
Solvent was evaporated, the residue redissolved in ethyl acetate (20 ml), washed with water (3
x 20 ml), and dried (magnesium sulfate). After removal of the solvent, the residue was
purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a
gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions
were combined and evaporated to give the desired product (273 mg).
MS fESP;>: 505 (MH*) for (yEWNA
NMRfDMSO-d^ 5: 1.25 (s,3H); 1.31 (s, 3H); 1.84 (m, 1H); 2.10 (m, 1H); 3.15 (m, 1H);
3.38 (dd, 1H); 3.50 (t, 1H); 3.63 (t, 1H); 3.81 (dd, 1H); 3.91 (m, 1H); 3.95-4.25
f (overlapping m, 6H); 4.79 (d, 2H); 5.08 (m, 1H); 6.69 (t, 1H); 7.01 (dd, 1H); 7.28 (dd,
1H); 7.57 (br, 1H); 7.75 (d, 1H); 8.14 (d, 1H).
The reagent for this compound was prepared as follows: (4SV2.2-DimethyM.3-dioxolan-4-ylmethyl 4-nitrophenyl carbonate (^iS)-2,2-Dimethyl-l,3-dioxolan-4-ylmethanol (362 mg, 2.74 mM) was dissolved in pyridine (9 ml), stirred at ambient temperature, and treated in portions with 4-nitrophenyl chloroformate (552 mg, 2.74 mM). After 6 hours, solvent was evaporated, the residue redissolved in ethyl acetate (15 ml), washed with water (15 ml), sodium bicarbonate solution (15 ml), brine (15 ml), and dried (magnesium sulfate). Removal of the solvent gave the product as an oil sufficiently pure for further use (858 mg). MS ffiSP): 298 (MH*) for C13HlfN07
NMR fDMSO-d^ 6: 1.28 (s,3H); 1.34 (s,3H); 3.74(dd,lH); 4.05 (t, 1H); 4.20 (dd, 1H); 4.25(dd,2H); 7.54 (d,2H); 8.29 (d,2H).

Example 21: f5JgV3-f4-(f3J?V^-rf2SV2.3-DihydroxvpropvIo3cvcarbonyIamino^pyrrolidin-l-yl)-3-flttorophenyl)-5-fl.2.3-triazol-l-yImethyl)oxazolidin-2-one
yI)-3-fluorophenyl)-5-(l,2,3-Mazol-l-ylmethyl)oxazolidin-2-one (240 mg, 0.48 mM) in tetrahydrofuran (5 ml) was treated with hydrochloric acid (2M, 2 ml) and stirred at ambient temperature for 18 hours. Solid potassium carbonate was added to neutralise, and the mixture filtered, and the filtrate evaporated to dryness. The residue was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 10% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (170 mg). MS (ESP): 465 (MH+) for C^FNA
NMR (DMSO-d^ 8: 1.83 (hextet, IH); 2.10 (hextet, IH); 3.15 (s, IH); 3.17 (s, IH); 3.33 (t, 2H); 3.50 (t, IH); 3.60 (dd, IH); 3.80 (dd, IH); 3.84 (dd, IH); 3.97 (dd, IH); 4.05 (dd, IH); 4.09 (d, IH); 4.15 (t, IH); 4.54 (t, IH); 4.73 (d, IH); 4.80 (d, 2H); 5.08 (m, IH); 6.69 (t, IH); 7.00 (dd, IH); 7.27 (dd, IH); 7.43 (d, IH); 7.74 (d, IH); 8.13 (d, IH).
Example 22: r5/gV3-f4-ff3JeV3-(2-Methoxvetlioxvcarbonvlaniinn^pyrrolidin-l-yn-3-fluoropheny1)-5-fl.2.3-triazoI~l-ylmethyl)oxazolidiii-2-one
(Ji?)-3 oxazolidin-2-one hydrochloride (200 mg, 0.52 mM) was suspended by stirring in
dichloromethane (10 ml) at 0° and sodium bicarbonate solution (5 ml) added.
2-Methoxyethyl chloroformate (340 mg, 2.46 mM) was added, and the mixture stirred 4
hours, allowing the temperature to rise to ambient. The organic layer was separated, washed
with sodium dihydrogen phosphate (2%, 2x15 ml), water (15 ml) and dried (magnesium
sulfate). Filtration and evaporation gave the desired product (183 mg).
MS flESP^: 449 (MH^) for QoH^FNA
NMRfDMSO-d^ 8: 1.82 (hextet, IH); 2.10 (hextet, IH); 3.13 (m, IH); 3.24 (s,3H); 3.36
(t, IH); 3.48 (m, 4H); 3.79 (dd, IH); 4.05 (m, 3H); 4.16 (t, IH); 4.79 (d, 2H); 5.08 (m,
IH); 6.69 (t, IH); 7.01 (dd, IH); 7.28 (dd, IH); 7.51 (d, IH); 7.74 (d, IH); 8.13 (d, IH).

Example 23: (5R)V3-r4-rr3JgV3-f2-Hydroxyethoxycarbonylamino^pyrrolidiii-l-yn-3-flnorophenyIl-5-(L2.3-triazoI-t-yImethyI)oyazoIidm-2-one
The resin bearing the title compound bound via its terminal hydroxy group (200 mg, nominz 0.118 mM) was swelled in dichloromethane (2 ml) for 30 minutes. Excess solvent was drained, and a solution of trifluoroacetic acid (1% in dichloromethane, 1 ml) was added, and the mixture agitated at ambient temperature for 2 hours. The resin was washed repeatedly with dichloromethane (5x5 ml), and the combined washings concentrated. The gum so obtained was azeotroped with isohexane/dichloromethane (20 ml) to give the desired produc (40 mg).
MS (ESP): 435 (MET) for C19H23FN605
NMRfDMSO-d^ 5: 1.85 (hextet, 1H); 2.10 (hextet, 1H); 3.17 (m, 1H); 3.28 (dd, 1H); 3.41 (dd, 1H); 3.51 (m, 2H); 3.82 (dd, 1H); 3.97 (t, 1H); 4.12 (m, 1H); 4.17 (t, 1H); 4.29 (m, 1H); 4.55 (m, 1H); 4.81 (d, 2H); 5.10 (m, 1H); 6.69 (t, 1H); 7.01 (dd, 1H); 7.27 (dd, 1H); 7.46 (d, 1H); 7.75 (d, 1H); 8.15 (d, 1H); 1 x OH exchanging, not seen.
The intermediates for this compound were prepared as follows: A polystyrene resin derivatised with 2-hydroxyethoxy-2'-chlorotrityl functionality (Novabiochem, 0.59 mM/g, 250 mg, 0.148 mM) was swelled in base-washed dichloro¬methane (3 ml) for 30 minutes, then excess dichloromethane drained. A solution of 4-nitrophenyl chloroformate (149 mg, 0.738 mM) and pyridine (175 mg, 2.22 mM) in base-washed dichloromethane was added, and the mixture shaken gently for 18 hours at ambient temperature. Solvent was then drained, and the resin washed with several portions of dichloromethane, then diethyl ether and dried in a desiccator. IR: 1768; 1596; 1264 cm'1.
The above resin (200 mg, nominally 0.118 mM) was swelled miV^-dimethylacetamide (3 ml) for 30 minutes, solvent drained, and a pre-mixed solution of (5i?)-3-(4-((3i?)-3-ammopyrroHo%-l-yl)-3-fiuorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxa2oUdm-2-one hydrochloride (226 mg, 0.59 mM) and dnsopropylethylamine (228 mg, 1.77 mM) in AyV"-dimethylacetamide (3 ml) added. The mixture was shaken gently for 4 hours at ambient temperature. Solvent was then drained, and the resin washed with 7^-dimethylacetamide (3

x 4 ml), then dichloromethane (3x4 ml), and dried in a desiccator: IE: 3409; 1758; 1725 compound"1.
Example 24: (5R)3-f4-((3S-3-(t-BntoTvcarhonvnaniinopvrroIidin-l-ylV3-fluoro~ phenyl)-5-(1.2.3-triazol-l-ylmethyI)oxazoIidm-2-one
(5i2)-3-(4-((5iS)-3-^Butoxycarbonyl)ammopyrroUdin-l-yl)-3-fluorophenyl)-5-azidomethyl-oxazolidin-2-one (3.2 g, 7.61 mM) was reacted by essentially the technique of Example 17 and purified by chromatography on a 60 g silica Biotage column, eluting with a gradient increasing in polarity from 0 to 7% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (1.66 g). MS (ESVY. 447 (MH4) for Q^FNA
NMR fDMSO-d^ 6: 1.39 (s, 9H); 1.84 (m, IH); 2.10 (m, IH); 3.12 (m, IH); 3.27 (t, IH); 3.38 (m, IH); 3.50 (t, IH); 3.83 (dd, IH); 4.06 (m, IH); 4.18 (t, IH); 4.82 (d, 2H); 5.11 (m, IH); 6.71 (t, IH); 7.03 (dd, IH); 7.13 (br, IH); 7. 30 (dd, IH); 7.77 (d, IH); 8.16 (d, IH).
The intermediates for this compound were prepared as follows:
3-Fluoro-4-rri^-3-r^bntoxycarbony^aminopviTolidin-l-yDnitrobenzene
Using essentially the technique for the equivalent intermediate in Example 17, but starting
from (5iS)r3-(^butoxycarbony)laminopyrroUdine (20 g, 0.108 M), gave the desired product as
a yellow solid (33.5 g), of sufficient quality for use without purification.
MS fESP): 326 (MH4) for C15H20FN3O4
NMR fDMSO-ayi 5: 1.36 (s,9H); 1.87 (m, IH); 2.08 (m, IH); 3.36 (m, IH); 3.54 (m, IH);
3.62 (tm, IH); 3.73 (m, IH); 4.09 (m, IH); 6.72 (t, IH); 7.19 (d, IH); 7.88 (overlapping m,
2H).
5-Anu^o-2-((3^-3-r^butoxvcarbonvnaminopyrrolidm-1-yl)fluorobenzene Using essentially the technique for the equivalent intermediate in Example 17, but starting from S-fluoro^-^i^-S-^butoxycarbony^ammopyrroUdm-l-y^nitrobenzene (33.5 g, 0.103 M), gave the desired product as an oil of sufficient quality for use without purification (-30

5-Ethoxycarbonylammo-2-((3iS)-3-(^b^
(35.2 g, 0.096 M). was dissolved in dry tetrahydrofuran (400 ml) under nitrogen, cooled to -70°, and treated dropwise over 20 minutes with a solution of lithium f-butoxide, prepared from f-butanol (9.3 g, 123 mM) in dry tetrahydrofuran (70 ml) and n-butyl lithium (66 ml, 1.6M in hexane). After stirring for 20 minutes, (i?)-glycidylbutyrate (15.2 g, 0.102 M) in tetrahydrofuran (20 ml) was added over 10 minutes, and the temperature allowed to rise to ambient over 16 hours. The mixture was treated with methanol (10 ml), stirred at ambient temperature for 10 minutes, then treated with a mixture of 5% aqueous sodium bicarbonate (250 ml) and ethyl acetate (500 ml). The precipitate was collected and washed well with ethyl acetate and water to give the desired product (19.5 g). The filtrate was separated into an organic layer, which was dried (magnesium sulfate) and evaporated The residue was refluxed briefly with ethyl acetate (100 ml), cooled, and filtered to give further product (16.6

MS (TBSP): 396 (MB4) for C19H26FN305
NMR (DMSO-d^ 5: 1.37 (s, 9H); 1.79 (m, 1H); 2.07 (m, IK); 3.08 (m, 1H); 3.24 (m overlapping H20, ~1H); 3.36 (m, 1H); 3.48 (tm, 1H); 3.53 (d, 1H); 3.63 (d, 1H); 3.74 (dd, 1H); 3.99 (t, 1H); 4.04 (m, IK); 4.63 (m, 1H); 5.15 (s, 1H); 6.71 (t, 1H); 7.08 (dd over¬lapping br, 2H); 7.39 (dd, 1H).
r5i?V3-(4-((3^-3-(^Butoxycarbonyl)anunopyiToHdm-l-ylV3-fluorophenyl)-5-methane-sulfonyloxymethyloxazQlidin-2-one
(5J2)-3-(4-((56)-3-^Butoxycarbonyl)anrniopyrroUdm-l-yl)-3-fluorophenyl)-5-hydroxy-methyloxazolidin-2-one (3.04 g, 7.7 mM) was suspended in a mixture of dichloromethane (25 ml) and pyridine (20 ml), cooled under nitrogen to 0°, and treated with triethylamine (1.15 g, 11.4 mM). Methanesulfonyl chloride (1.04 g, 9.1 mM) in dichloromethane (5 ml) was added dropwise, and the mixture stirred 45 minutes at the same temperature. The mixture was concentrated to dryness, and the residue dissolved in ethyl acetate (70 ml), then washed with 5% sodium bicarbonate (70 ml), water (2 x 70 ml), brine (70 ml), and dried (magnesium sulfate). After evaporation and azeotroping with toluene (20 ml), product of sufficient quality was obtained for use without further purification (3.64 g). MS rESP): 474 (MB4) for C2DH28FN307S
NMR rPMRO-d^ 5: 1.37 (s, 9H); 1.81 (m, 1H); 2.08 (m, 1H); 3.11 (m, 1H); 3.26 (s, 3H); 3.28 (m, 1H); 3.38 (m, IK); 3.49 (tm, IK); 3.76 (dd, 1H); 4.05 (m, IK); 4.11 (t, 1H); 4.43 (dd, IK); 4.50 (dd, IK); 4.96 (m, IK); 6.72 (t, IK); 7.10 (dd, IK); 7.16 (d, IK); 7.49 (dd, IK).
f5igV3-r4-r^^-3~^Buto\^carbonvnaminopvrrolidin4-v1V3-fluoropheny1V5-azidomethvl-oxazolidin-2-one
(5i?)-3-(4-((3iS)-3-(^Butoxycarbonyl)arxitnopyrrohdm-l-yl)-3-fluorophenyl)-5-methane-sulfonyloxymethyloxazolidin-2-one (3.6 g, 7.61 mM) was dissolved in A^V'-dimethyl-formamide (40 ml), treated with sodium azide (0.99 g, 15.2 mM), and heated with stirring at 80° for 3.5 hours. After cooling the mixture was diluted with water (400 ml), and extracted into ethyl acetate (400 ml). The combined organics were washed with water (2 x 400 ml) and

brine (200 ml), dried (magnesium sulfate), and evaporated to give the required product (3.2
g)-
MS (ESP): 421 (MH*) for C19H25FN604
Example 25: f5J?V3-r4-fr3^-3-AminopyrroIidiii-l-vn-3-fluorophenylV5-a.2.3-triazo1-l-ylmethyl)oxazoIidm-2-one
(5i?)-3-(4-((itf)-3-^Butoxycarbonyl)a
l-ylmethyl)oxazolidin-2-one (1.55 g, 3.47 mM), was dissolved in dichloromethane (8 ml),
and treated with a solution of hydrogen chloride in ethanol (3.8M, 40 ml). After stirring 2
hours at ambient temperature, the mixture was evaporated to dryness to give product as a
hydrochloride of sufficient quality to require no purification (1.64 g).
MS (ESP): 347 (MET) for C16H19FN602
NMRfl3MSO-df) 6: 2.00 (m, IH); 2.25 (m, IH); 3.24 (dd, IH); 3.41 (m, IH); 3.52 (m,
2H); 3.82 (overlapping m,2H); 4.17 (t, IH); 4.81 (d,2H); 5.10 (m, IH); 6.78 (t, IH); 7.06
(dd, IH); 7.33 (dd, IH); 7.76 (d, IH); 8.17 (d, IH); 8.36 (br, ~2H).
Example 26: r5J?V3-r4-fr^-3-AcetamidopyrroIidin-l-yn-3>flnorophenvn-5-f 1.2.3-triazol-l-ylmethyl)oxazolidip-2-one
Using essentially the technique of Example 19, but starting from (5iZ)-3-(4-((55)-3-ammopyiroHdm-l-yl)-3-fluorophenyl)-5-(l,2,3-1riazol-l-ylmemyl)oxazoUdin-2-one hydrochloride (250 mg, 0.65 mM), and replacing the methyl chloroformate with acetic anhydride gave the desired product (150 mg). MS (ESP): 405 (MET) for C18H21FN603
NMR fDMSO-d,) S: 1.87 (s overlapping m, 4H); 2.16 (m, IH); 3.18 (m, IH); 3.33 (dd, IH); 3.46 (t, IH); 3.56 (tm, IH); 3.88 (dd, IH); 4.24 (t, IH); 4.35 (m, IH); 4.88 (d, 2H); 5.15 (m,lH); 6.89 (t, IH); 7.08 (dd, IH); 7.37 (dd, IH); 7.84 (d, IH); 8.19 (d, IH); 8.23 [d, IH).

Using essentially the technique of Example 19, but starting from (5if)-3-(4-((55)-3-
ammopyrroh^n-l-yl)-3-fiuorophenyl)-5-(l,2,3-M
hydrochloride (250 mg, 0.65 mM) gave the desired product (192 mg).
MS (ESP): 405 (MET) for ClgH21FN604
NMR fDMSO-d£) 5: 1.82 (m, 1H); 2.11 (m, 1H); 3.13 (m, 1H); 3.31 (m overlapping H20,
~2H); 3.51 (s overlappingm, 4H); 3.81 (dd, 1H); 4.07 (m, 1H); 4.17 (t, 1H); 4.80 (d, 2H);
5.08 (m, 1H); 6.71 (t, 1H); 7.02 (dd, 1H); 7.27 (dd, 1H); 7.47 (d, 1H); 7.76 (d, 1H); 8.15
(d, 1H).
Example 28: (5Jg)-3-f4-rf.?,V)-3-Methanesulfonamidopvrro]idin-l-vlV3-fli]nrophenvTV5-(1.2.3-triazol-l -yImethyl)oxazolidin-2-one
(5J?)-3 MS (ESP): 425 (MH4) for C17H21FN60 NMR fDMSO-dJ 8: 1.84 (m, 1H); 2.18 (m, 1H); 2.93 (s, 3H); 3.18 (m, 1H); 3.34 (m overlapping H20,~2H); 3.54 (t, 1H); 3.80 (dd, 1H); 3.96(dd,lH); 4.15 (t, 1H); 4.49 (d, 2H); 5.08 (m, 1H); 6.71 (t, 1H); 7.01 (dd, 1H); 7.28 (dd, 1H); 7.34 (d, 1H); 7.74 (d, 1H); 8.13 (d, 1H).

EmmDle29: (SjR)^-r4-Tmidazoi-l-vI-3-fluoroiyhenvl).5-n.2.3-triazol-l-vlmethyl)-oxazolidin-2-one
(5i?)-3-(4-Imidazol-l-yl-3-fluoroplienyl)-5-a2idomethyloxazolidiii-2-one (755 mg, 1.35 rnM)
was dissolved in dioxane (40 ml), treated with norbornadiene (1.15 g, 12.5 mM) and heated
under reflux for 16 hours. After removal of the solvent, the residue was dissolved in the
minimum of dichloromethane and purified by chromatography on a 20 g silica Mega Bond •
Elut® column, eluting with a gradient increasing in polarity from 0 to 10% methanol in
dichloromethane. Relevant fractions were combined and evaporated to give the desired
product (660 mg).
MS (PSg): 329 (MIT) for C15H13FN602
NMRiRMSQ^ 8: 3.95 (dd, 1H); 4.29 (t, 1H); 4.85 (d, 2H); 5.16 (m, 1H); 7.11 (d, 1H);
7.39 (dd, 1H); 7.54 (overlapping m, 2H); 7.66 (d, 1H); 7.77 (d, 1H); 7.98 (m, 1H); 8.18 (d,
1H).
(Intermediate oxazolidinone described in Upjohn WO 96-23788)
Example30: f5K)-3-(4-ImidazoI-1 -vl-3-fluorophenvn~5-fl-pviazoIyl)methyI)oxazoIidin-?-one
Sodium hydride (60% in oil, 32 mg, 0.8 mM) was stirred under nitrogen in A^AT-dirnethylformamide (2 ml), pyrazole (68 mg, 1 mM) added, and stirring continued for 10 minutes. (5R)-3 -(4-hnidazoM -yl-3-fluorophenyl)-5-methanesiifonyloxymethyloxazolidin-2-one (142 mg, 0.4 mM) was dissolved in iV^-dimethylformarnide (1 ml)* added to the above, and the mixture stirred 18 hours at ambient temperature. After diluting with 5% aqueous sodium bicarbonate (30 ml), the mixture was extracted with ethyl acetate (50 ml), the extract cashed with water (2x 30 ml), brine (25 ml), dried (magnesium sulfate) and evaporated. The residue was dissolved in the rninirmiTn of dichloromethane and purified by chromatography on i 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 ;o 15% isopropanol in dichloromethane. Relevant fractions were combined and evaporated, hen dissolved in dichloromethane (5 ml) and stirred for 18 hours with PS-Isocyanate resin Argonaut Technologies, 500 mg) to remove ring opened impurities. Filtration and ivaporation gave the desired product (34 mg). v£S (ESP.): .328 (Mir) for C16HI4FNA

NMRtpMSO-dJ 8: 3.89 (dd, 1H); 4.17 (t, 1H); 4.46 (d, 2H); 5.04 (m, 1H); 6.21 (t, 1H); 7.08 (m, 1H); 7.32 (dd, 1H); 7.39 (d, 1H); 7.50 (m, 1H); 7.58 (t, 1H); 7.60 (dd, 1H); 7.72 ' (d, 1H); 8.00 (m, 1H). (Intermediate described in WO 96-23788)
Example 31: (5ig)-3-(4-Imidazol-l-yl-3-fluorophenyl)-5-tetrazoI-l-ylmethyloxazolidm-2-oneand(5R)-3-(4-ImidazoI-l-yl-3-fluoropheny))-5-tetrazoI-2-ylmethyloxazoIidm-2-ope
(5J?)-3-(4-Inn^azol-l-yl-3-fluorophenyl)-5-memanesulfonyloxymemyloxazoUdm
mg, 0.7 mM) was dissolved in A^A^dimethylformamide (2 ml), treated with li7-tetrazole (123
mg, 1.75 mM) and potassium carbonate (241 mg, 1.75 mM), and heated at 95° for 3 hours.
After cooling, the mixture was diluted with water (30 ml), extracted with ethyl acetate (50
ml), the extract washed with water (2x 30 ml), brine (25 ml), dried (magnesium sulfate) and
evaporated. The residue was dissolved in the minimum of dichloromethane and purified by
chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing
in polarity from 0 to 10% isopropanol in dichloromethane, then 0 to 20% methanol in
dichloromethane. Relevant fractions were combined and evaporated, the first eluting product
being the 2-isomer (80 mg).
MS (ESP): 330(MH+)forC14H12FN7O2
NMR (DMSO-dg) 8: 3.96(dd,lH); 4.34 (t,lH); 5.26 (overlapping m, 3H); 7.12 (m, IB);
7.40 (dd, 1H); 7.55 (d, 1H); 7.66 (t overlapping dd, 2H); 8.00 (m, 1H); 9.05 (s, 1H).
The second eluting product was the 1-isomer (51 mg).
MS (ESP): 330(MB+)forC14H12FN7O2
NMR rDMSO-d^ 8: 3.98 (dd, 1H); 4.31 (t, 1H); 4.95 (m, 2H); 5.21 (m, 1H); 7.12 (m,
IB); 7.43 (dd, 1H); 7.55 (d, IB); 7.67 (t overlapping dd, 2H); 8.01 (m, 1H); 9.49 (s, 1H).
Intermediate described in WO 96-23788.
Example 32: f5ift-3-(4-f4-HvdroxymethvIimidazoM -vn-3-fluorophenvlV5-tetrazoI-l-
^lmethyIoxazoIidin-2-oneand(5RV3-(,4-r4-Hydroxymethylimidazol-l-yl)-3-
nuorophenyIV5-tetrazol-2-yImethyIoxazoIidin-2-one
'5if)-3-(4-(4-^Buryldmiemylsilyloxymemyh^mdazol-l-yl)-3-fluorophenyl)-5-hydroxy-nemyloxazolidin-2-one (421 mg, 1 mM), l#-tetrazole (105 mg, 1.5 mM), and triphenyl-

phosphine (393 mg, 1.5 mM) were dissolved by stirring in dry tetrahydrofuran (5 ml) under nitrogen in an ice-bath. Diisopropylazodicarboxylate (303 mg, 1.5 mM) was added dropwise, and the mixture stirred 2 hours, allowing the temperature to rise to ambient. The mixture was cooled to 0°, treated with trifluoroacetic acid (5 ml), and stirred 30 rninutes at ambient temperature. The mixture was diluted with ethyl acetate (100 ml), and extracted with aqueous
hydrochloric acid (1M, 100 ml). The acid extract was washed with ethyl acetate (100 ml),
then made basic with concentrated aqueous ammonia, and reextracted with dichloromethane.
After drying (magnesium sulfate), the residue was purified by chromatography on a 10 g silica
Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 10%
methanol in dichloromethane. Relevant fractions were combined to give the less polar
tetrazol-2-yl isomer (105 mg).
MS fESP^l: 360 0vnr)forC15H,4FN7O3
NMRfDMSO-dg) 8: 3.96 (dd, 1H); 4.32 (t, 1H); 4.39 (d, 2H); 4.96 (t, 1H); 5.16 (dd, 1H);
5.25 (dd, 1H); 5.31 (m, 1H); 7.32 (d, 1H); 7.38 (dd, 1H); 7.63 (t, 1H); 7.66 (dd, 1H); 7.90
(d, 1H); 9.02 (s, 1H).
The aqueous ammonia liquors were cooled to 4° overnight, to precipitate crystals of the more
polar tetrazol-1 -yl isomer (6 mg).
MS (ESPV 360 (MIT) for C14H12FN702
The oxazolidinone intermediate is described in WO 97-31917.
Example33: f5Jfl-3-f4-f2-MethvlimidazoM-vn-3-fliiorophenvr>-5-tetrazol-1 -vl-
methyIoxazolidm-2-oneand(5i?V3-r4-r2-Methylimidazol-l-yI)-3-flaorophenyI)-5-
tetrazol-2-yImethyIoxazoIidm-2-one
Essentially the technique of Example 17 was used, but starting from (5i?)-3-(4-(2-memylimidazol-l-yl)-3-fluorophenyl)-5-hydroxymethyloxazoUdin-2-one (582 mg, 2 mM). Crude material from the acid extract was purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 20% methanol in dichloromethane. Relevant fractions of the first eluting product were combined to give the less polar tetrazol-2-yl isomer (246 mg). MS fESP): 344 (MIT) for CI5H14FN702 NMR fDMSO-d^ 5: 2.14 (s, 3H); 3.97 (dd, 1H); 4.34 (t, 1H); 5.16 (dd, 1H); 5.26 (dd,

IH); 5.32 (m, IH); 6.91 (d, IK); 7.20 (d, IK); 7.40 (dd, IH); 7.54 (t, IK); 7.66 (dd, 1H);
9.02 (sa IH).
The second eluting product was the 1-isomer (210 mg).
MSilSE): 344 (MET) for C15H14FN702
NMR (DMSO-d^ 8: 2.13 (s, 3H); 3.97 (dd, IH); 4.31 (t, IH); 4.94 (d, 2H); 5.21 (m, IH);
6.91 (d, IH); 7.20 (d, IH); 7.42 (dd, IH); 7.55 (t, IH); 7.67 (dd, IH); 9.47 (s} IH).
The intermediates for these compounds were prepared as follows:
3-Fluorn-4~(2-methylimidazol-]["yl)nitrobenzene
2-Methylimidazole (9.02 g, 0.11 M) and N,N-diisopropylemylarnine (32.2 g, 0.25 M) were
dissolved in acetonitrile (160 ml), and 3,4-difluoromtrobenzene (15.9 g, 0.1 M) added. The
mixture was stirred and heated to reflux under nitrogen for 24 hours. Solvent was evaporated,
the residue dissolved in ethyl acetate (300 ml), washed with water (150 ml), brine (150 ml),
and dried (magnesium sulfate). The residue was recrystallised from a mixture of ethyl acetate
(25 ml) and cyclohexane (150 ml) with the addition of charcoal to give the title compound
(11.5 g),mp 106-107°.
M3_Q3£E): 222 (MH1) for C10HgFN3O2
NMR fDMSO-d_;> 6: 2.25 (s, 3H); 7.00 (d, IH); 7.35 (t, IH); 7.87 (t, IH); 8.23 (dd, IH);
8.43 (dd, IH).
5-Amino-2-(2-methylimidazol-l-vnfluorobenzene
3-Fluoro-4-(2-methylimidazol-l-yl)nitrobenzene (40 g, 0.181 M) was dissolved in a mixture of methanol (200 ml) and tetrahydrofuran (800 ml), cooled to 0° under nitrogen, and treated with ammonium formate (57 g, 0.905 M) followed by palladium on charcoal (10%, 2 g). The mixture was stirred at ambient temperature for 18 hours, filtered through celite, celite washed with methanol (100 ml), and filtrate evaporated to dryness. The residue was partitioned between ethyl acetate (800 ml) and 10% aqueous sodium bicarbonate (250 ml). The organic layer was separated, washed with brine (250 ml), dried (magnesium sulfate) and evaporated to give title compound (34.6 g). _MS flESP): 192 (MH*) for C10H10FN3

NMR CPMSO-dJ 5: 2.08 (s, 3H); 5.68 (s, 2H); 6.45 (overlapping m, 2H); 6.84 (d, 1H); 7.03 (overlapping m, 2H).
5-Benzvloxvcarhonylamino-2-r2-methvlimidazol-l-yDfluorobenzene 5-Arrmio-2-(2-memylimidazol-l-yl)fluorobenzene (34.25 g, 0.179 M) was dissolved in dry dichloromethane (600 ml) under nitrogen, and cooled to -5°. Pyridine (17.7 g, 0.224 M) was added, followed by benzyl chloroformate (33.7 g, 0.197 M) over 20 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 250 ml) was added, the organic layer separated, the aqueous layer re-extracted with dichloromethane (2 x 300 ml), and combined extracts dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (400 ml) to give title product (54.5 g). MS^ESE): 326(MH+)forC18H16FN302
NMRfDMSO-d^ S: 2.13 (s, 3H); 5.18 (s, 2H); 6.89 (s, 1H); 7.17 (s, 1H); 7.41 (overlapping m, 7H); 7.73 (dd, 1H); 10.21 (br, 1H).
(5Jg)-3-(3-Fluoro-4-(2-methylmiida7.ol-l-yl)phenylV5-hydroxymethyloxazolidin-2-one 5-Benzyloxycarbonylammo-2-(2-methylimidazol-l-yl)fluorobenzene (54 g, 0.166 M) was dissolved in a mixture of dry tetrahydrofuran (600 ml) and 1,3-dimethyl-tetrahydropyrirnidin-2-one (100 ml) under nitrogen, cooled to -70°, and treated with a solution of n-butyllithium (1.6M in isohexane, 1.14 ml), over 30 minutes. After stirring for 30 minutes at -70°, a solution of (iO-glycidylbutyrate (26.35 g, 0.183 M) in dry tetrahydrofuran (50 ml) was added over 15 minutes. Stirring was continued for 16 hours allowing the temperature to rise to ambient. The mixture was treated with aqueous sodium bicarbonate (5%, 500 ml) and ethyl acetate (800 ml), the organic layer separated, and the aqueous extracted with further ethyl acetate (3 x 750 ml). The combined extracts were dried (magnesium sulfate) and evaporated, and the resulting oil triturated with diethyl ether. The resulting solid was recrystallisd from isopropanol to give the title compound (21.5 g). MS (ESP): 292 (MH4) for C, jvrivQlfDMSO-d^ S: 2.16 (s,3H); 3.56 (dt, 1H); 3.69 (dt, 1H); 3.88 (dd, 1H); 4.15 (t,lH); 4.74 (m, 1H); 5.24 (t, 1H); 6.92 (s, 1H); 7.20 (s, 1H); 7.48 (dd, 1H); 7.53 (t, 1H); 7.74

(dd, 1H).
Example 34: (5JgV.^-f4-f4-Methylimidazol-l-yIV3-fliiomphenvlV5-tetrazol-l-yl-methyloxazoIidin-2-one and f5gV3-f4-f4-MethvIimidazo]-1 -yIV3-fluorophenyIV5-tetrazol-2-ylmethvIoxazoIidm-2-one
Sodium hydride (50% in oil, 108 mg, 2.25 mM) was stirred m JV^-dunethylformamide (3 ml) under nitrogen, and l#-tetrazole (158 mg, 2.25 mM), dissolved m A^-dimethylformamide (4 ml) added. After stirring for 10 minutes, (5i?)-3-(4-memylimidazol-l-yl-3-fiuorophenyl)-5-methanesuIfonyIoxymethyloxazolidin-2-one (553 mg, 1.5 mM) was added, the mixture heated to 80° for 4 hours. The mixture was diluted with aqueous sodium bicarbonate (30 ml), extracted with ethyl acetate (3 x 20 ml), and the extract washed with water (2 x 20 ml), and brine (20 ml). After drying (magnesium sulfate) and evaporation, the residue was purified by chromatography on a 20 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 20% methanol in dichloromethane. Relevant fractions of the first eluting product were combined to give the less polar tetrazol-2-yl isomer (269 mg).
MSiESE): 344(MHVorC15HMFN702
NMR fDMSO-d^ 8: 2.15 (s, 3H); 3.96 (dd, 1H); 4.34 (t, 1H); 5.17 (dd, 1H); 5.27 (dd,
1H); 5.33 (m, 1H); 7.21 (d, 1H); 7.37 (dd, 1H); 7.63 (t, 1H); 7.66 (dd, 1H); 7.87 (d, 1H);
9.04 (s, 1H).
The second eluting product was the 1-is'omer (166 mg).
MSiESJP): 344 (MET) for C^FNA
NMR(DMSQ-d^ 5: 2.16 (s, 3H); 3.97 (dd, 1H); 4.31 (t, 1H); 4.96 (d, 2H); 5.21 (m, 1H);
7.21 (d, 1H); 7.39 (dd, 1H); 7.62 (t, 1H); 7.66 (dd, 1H); 7.87 (dd, 1H); 9.48 (s, 1H).
The intermediates for these compounds were prepared as follows:
3-Fluoro-4-(4-methvlimidazol-l-yl)nitroben2ene
4-Memylimidazole (45.1 g, 0.55 M) and 7y;N-du^opropylethylamine (161 g, 1.25 M) were dissolved in acetonitrile (800 ml), and 3,4-difluoronitrobenzene (79.5 g, 0.5 M) added. The mixture was stirred and heated to reflux under nitrogen for 24 hours. Solvent was evaporated, the residue dissolved in ethyl acetate (800 ml), washed with water (400 ml), brine (200 ml),

and dried (magnesium sulfate). The residue was dissolved in toluene (250 ml), treated with
charcoal, filtered, and diluted with hot cyclohexane (75 ml) to crystallise 3-fhioro-4-(4-
memylimidazol"l-yl)nitrobenzene (64.7 g).
MS (ESQ: 222 (MET) for C10H8FN3O2
NMRfpMSO-ds) 5: 2.18 (s, 3H); 7.29 (s, 1H); 7.92 (t, 1H); 8.07 (s,lH); 8.18(dd,lH);
8.38 (dd, 1H).
5-Arrmio-2-r4-memvlirnidazol-1-ynfluorobenzene
3-Fluoro^-(4-memylirnidazol-l-yl)nitrobenzene (64.7 g, 0.293 M) was dissolved in a mixture of methanol (200 ml) and tetrahydrofuran (800 ml), cooled to 0° under nitrogen, and treated with ammonium formate (99.3 g, 1.46 M) followed by palladium on charcoal (10%, 2.5 g). The mixture was stirred at ambient temperature for 48 hours, filtered through celite, celite washed with methanol (200 ml), and filtrate evaporated to dryness. The residue was partitioned between ethyl acetate (800 ml) and 10% aqueous sodium bicarbonate (250 ml). The organic layer was separated, washed with brine (250 ml), dried (magnesium sulfate) and evaporated to give title compound (50.6 g). MS (ESP): 192(MH^forC10H10FN3
NMRtoMSO-d^ 5: 2.12 (s, 3H); 5.60 (br s, 2H); 6.42 (dd, 1H); 6.47 (dd, 1H); 6.98 (s, 1H); 7.11 (t,lH); 7.60 (s,lH).
5-Benzyloxycarbonylamino-2-(4-methylirnidazol-l-yl)fluorobenzerie 5-Ammo-2-(4-memylimidazol-l-yl)fluorobenzene (50.6 g, 0.265 M) was dissolved in dry dichloromethane (800 ml) under nitrogen, and cooled to -5°. Pyridine (26.1 g, 0.33 M) was added, followed by benzyl chloroformate (49.9 g, 0.292 M) over 30 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium' bicarbonate (5%, 350 ml) was added, the organic layer separated, and the aqueous layer re-extracted with dichloromethane (2 x 200 ml), and combined organics dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (300 ml) to give title product (80 g). MS (ESP): 326(MH0forClgH]6FN3O2 [sfMR (DMSO-d^ 8: 2.15 (s, 3H); 5.16 (s, 2H); 7.13 (s, 1H); 7.31 (dd, 1H); 7.41 (m, 5H);

7.48 (t, IK); 7.57 (dd, IK); 7.78 (s, 1H); 10.15 (br s, IK).
r5JgV3~r3-Fluoro-4-(4-rnethy1imidazol-l-yl)phenv1V5-hvdroxymemy1oxazolidiTi-2~r>Tift 5-Benzyloxycarbonylarnmo-2-(4-memylimidazol-l-yl)fluorobenzene (54 g, 0.166 M) was 5 dissolved in a mixture of dry tetrahydrofuran (600 ml) and 1,3-dimemyl-tetrahydropyrhiudin-2-one (100 ml) under nitrogen, cooled to -70°, and treated with a solution of n-butyllithium (1.6M in wohexane, 114 ml), over 30 minutes. After stirring for 30 minutes at -70°, a solution of (i?)-glycidylbutyrate (26.35 g, 0.183 M) in dry tetrahydrofuran (50 ml) was added over 15 minutes. .Stirring was continued for 16 hours allowing the temperature to rise to ambient. ) The mixture was treated with aqueous sodium bicarbonate (5%, 500 ml) and ethyl acetate (800 ml), and undissolved solid was removed and washed well with diethyl ether to give title product (16.3 g).
The aqueous layer was further extracted with ethyl acetate (2 x 750 ml), the combined extracts dried (magnesium sulfate) and evaporated, and the residue triturated with diethyl ether. The resulting solid was recrystallised from ethanol to give more product (10.9 g).
MS (ESP): 292(MHVorCMHMFN303
NMR fDMSO-dJ 8: 2.13 (s, 3H); 3.56 (dd, IK); 3.68 (dd, IK); 3.86 (dd, IK); 4.11 (t, 1H); 4.73 (m, IK); 5.21 (br, IK); 7.18 (s, IK); 7.45 (dd, IK); 7.60 (t, IK); 7.73 (dd, IK); 7.83 (s, IK).
(5Jn-3-f3-Fluoro-4-(4-methy1imidazol-U^ 2-one
(5iZ)-3-(3-Fluoro-4-(4-memylimidazol-1 -yl)phenyl)-5-hydroxymethyloxazohdin-2-one (11.8 g, 40.5 mM) was stirred in a mixture of pyridine (200 ml) and triethylamine (4.86 g, 48.2 mM) under nitrogen in an ice-bath. Methanesulfonyl chloride (5.16 g, 45 mM) was added dropwise, and the mixture stirred for 2 hours, allowing the temperature to rise to ambient. Solvent was evaporated, and the residue stirred vigorously with a mixture of aqueous sodium bicarbonate (5%, 200 ml) and isohexane (200 ml). The precipitate was filtered, washed with water then wohexane, and dried. The residue was recrystallised from hot acetone (200 ml) by dilution with isohexane (300 ml) to give the title product (11.7 g), mp 151-153°. MSXEI): 369 (M*) for C]5H16FN305S

NMRCPMSQ-dJ 5: 2.16 (s, 3H); 3.27 (s, 3H); 3.88 (dd, IH); 4.24 (t, IH); 4.47 (dd, IH); 4.54 (dd, IH); 5.04 (m, IH); 7.20 (d, IH); 7.45 (dd, IH); 7.63 (t, IH); 7.73 (dd, IH); 7.85 (UH).
Example 35: f5i?V3- (5i?)-3-(4-(l-Benzyl-l>2,5,6-tetrahyQ^opyridin-4-yl)-3,5-difluorophenyl)-5-hydroxy-methyloxazolidin-2-one (4.67 g, 11.6 mM), 3#-l,3,4-oxadiazol-2-one (1 g, 11.6 mM, J. Het. Chan., 1995, 32,123), and triphenylphosphine (4.58 g, 17.5 mM) were treated with toluene (50 ml) and evaporated to dryness at 50° to remove water traces. The residue was dissolved in dry tetrahydrofuran (100 ml) by stirring under nitrogen in an ice-bath. Diisopropylazo-dicarboxylate (3.53 g, 17.5 mM) was added dropwise, and the mixture stirred 2 hours, allowing the temperature to rise to ambient. Solvent was evaporated and the residue purified by chromatography on a 90 g silica Biotage column, eluting with a gradient increasing in polarity from 0 to 100% ethyl acetate in dichloromethane. Relevant fractions were combined to give the impure product (6.2 g), contaminated with triphenylphosphine oxide. A portion (2 g) of this material was applied in dichloromethane to a 10 g Isolute strong acid SCX column, and eluted with a gradient increasing in polarity from 0 to 50% methanol in dichloromethane to remove neutral impurities, and finally with a mix' of dichloromethane : methanol: concentrated aqueous ammonia 80:16:4. Solvent was evaporated from appropriate fractions, the residue taken up in 10% aqueous phosphoric acid, and reprecipitated with ammonia to give the title product (275 mg). MS (RSP): 469 (MH4) for C^H^NA
NMR (DMSO-d^ 6: 2.29 (br, 2H); 2.62 (t, 2H); 3.03 (m, 2H); 3.57 (s, 2H); 3.86 (dd, IH); 4.01 (dd, IH); 4.11 (dd, IH); 4.18 (t, IH); 5.00 (m, IH); 5.78 (s, IH); 7.27 (d, 2H); 7.33 (m, 5H); 8.45 (s, IH).

Example 36: r5ig^-3-r4-ri-BenzyI-1.2.S.6-tetrahydropyridin-4-ylV3.5-difluorophenyIV^-r2-oxo-3H-1.3.4-thiadiazol^3-y1methynoxazoIidin-2-one
Essentially the procedure of Example 35 was used, but starting with (5R)-3-(4-(l-benzyl-
l,2,5,64etrahydropyridm-4-yl)-3,5-difluoropte
mg, 2 mM), and 3#-l,3,4-thiadiazol-2-one (214 mg, 2.2 mM, Helv. Chim. Acta, 1982, 65,
2606), and stirring the reaction for 18 hours. After elution from the SCX column, the gum
after evaporation was triturated with diethyl ether to give the desired product (291 mg).
MS (ESK): 485 (MH4) for C^H^NAS
NMR fDMSO-d^ 8: 2.29 (br, 2H); 2.60 (t, 2H); 3.03 (m, 2H); 3.57 (s, 2H); 3.85 (dd, IH);
4.18 (overlapping m, 2H); 4.29 (dd, IH); 5.03 (m, IH); 5.76 (s, IH); 7.26 (d, 2H); 7.32 (m,
5H); 8.56 (s^ IH).
Example 37: r5^-3-f4-f3.6-Dihydro-2g-pvraii-4-vl>-3-fliiorophenyn-5-f3-methvl-2-oxo-2.3-dihydrojmidazoI-l -ylmethyl) oxazoIidin-2-on e
A. solution of l-methyhrnidazolidin-2-one (80 mg, 0.82 mM, Heterocycles, 1987,26, 3153) in irmethylsulfoxide (1 ml) was treated with sodium hydride (55% in oil, 40 mg, 0.92 mM) at ambient temperature under nitrogen. After stirring for 20 minutes, (5JR)-3-(4-(3,6-dihydro-ZH-pyran-4-yl)-3-fiuorophenyl)-5-memanesulfonyloxymemyloxazoHdin-2-one(300mg, 3.81 mM; WO 97-09328) in dimethylsulfoxide (1.5 ml) was added and stirring continued for 1.5 hours. The temperature was then progressively raised to 85°, and heated at this :emperature for 24 hours. After cooling and dilution with water (50 ml), the mixture was jxtracted witii ethyl acetate (3 x 30 ml), and combined extracts washed with brine (20 ml). \fter drying (magnesium sulfate) and evaporation, the residue was purified by chromato¬graphy on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in )olarity from 0 to 6% methanol in dichloromethane. Relevant fractions were combined to rive the title product (60 mg). 4S (ESP): 374(MH+)forC19H20FN3O4
NIMR (DMSO-d^ 8: 2.41 (s, 2H); 3.08 (s, 3H); 3.76-3.95 (overlapping m, 5H); 4.15 (t, .H); 4.20 (m, 2H); 4.92 (m, IH); 6.08 (s, IH); 6.50 (m, 2H); 7.25 (d, IH); 7.40 (m, 2H).

Example 38: (5J?V3-r4-n.fi-L^hydro-2Jy-pvran-4-yn-3-fluorophenvn-5-f3-metTiyl-2-thiQrQ-2.3-dihydroimidazol-l-ylmethynorazoIidin-2-one
Essentially the procedure of Example 37 was used, but starting with (5i?)-3-(4-(3,6-dihydro-2ZT-pyran-4-yl)-3-fluorophenyl)-5-methanesdfonyloxvme1nyloxazoHdin-2-one(300mg, 0.81 mM), and l-methyltmidazolidin-2-thione (100 mg, 0.88 mM) and heating the reaction at 60° for 1.5 hours. Chromatography on two columns gave the desired product (29 mg). MS (RSP): 390(Mir)forCli>H20FN3O3S
NMR (DMSO-d^ 8: 2.42 (br s, 2H); 3.46 (s, 3H); 3.80 (t, 2H); 4.02 (dd, IK); 4.20 [overlapping m,3H); 4.27-4.47 (m, 2H); 5.09 (m,lH); 6.09 (br s, 1H); 7.17 (m,2H); 7.29 [dd, 1H); 7.38 (d, IK); 7.45 (dd, 1H).
Example 39: r5i?V3-r4-Methv1thiophenvn-5-a.2.3-triazol-l-vlTnethvnoxazolidin-2-one
(JJ?)-3-(4-Methyltbiophenyl)-5-a2idomemyloxazohdin-2-one (1.62 g, 6.14 mM) was
iissolved in dioxane (30 ml), treated with norbomadiene (2.98 g, 31.5 mM) and heated under
eflux for 6 hours. After removal of the solvent, the residue was dissolved in the minimum of
lot ethyl acetate, filtered, cooled, then diluted with isohexane to precipitate the desired
>roduct (600 mg).
dS (CI): 291 (MIT) for C13H14N402S
4MR (270 MHz. CDCU 5: 2.46 (s, 3H); 3.92 (dd, 1H); 4.15 (t, 1H); 4.79 (m,2H); 5.04
m, IK); 7.23 (d, 2H); 7.31 (d, 2H); 7.74 (d, IK); 7.80 (d, 1H).
"he starting material is described by WA Gregory et al, J.Med.Chem., 1989,32,1673.
:xample40: (5gV3-f4-MethvlsulfnnvlphenvIV5-(1.2.3-triazol-l-yImethynoxazolidin-2-ne
;5Ji)-3-(4-MemyltMophenyl)-5 iM) was dissolved in dichloromethane (15 ml), treated with 3-chloroperoxy-benzoic acid
50%, 1.24 g, 3.59 mM), and stirred at ambient temperature for 3 hours. After removal of the
Dlvent, the residue was triturated with diethyl ether and filtered, to give the desired product
550 mg).
fS(CT>: 323 (MIT) for C13HI4N404S
MR (270 MHz. CDC^ + DMSO-d^) 5: 2.57 (s, 3H); 3.52 (dd, 1H); 3.78 (t, IK); 4.36 (m,

2H); 4.67 (m, IH); 7.18 (d, 2H); 7.26 (d, IH); 7.38 (d, 2H); 7.47 (d, IH).
Example 41: r5i?)-3-(4-f-BiitvIpheriyn-5-rt.2.3-triazol-1 -vlmethynoxazolidin-2-one
(5i?)-3-(4-f-Butylphenyl)-5-azidomethyloxazolidin-2-one (400 mg, 1.46 mM) was dissolved i in dioxane (8 ml), treated with norbomadiene (1.3 g, 14.1 mM) and heated under reflux for 6 hours. After removal of the solvent, the residue was dissolved ethyl acetate, and purified by flash chromatography on silica, eluting with the same solvent. Relevant fractions were combined to give the desired product (260 mg, mp 140-142°). MS (ED: 300 (M^) for ClfrH20N4O2
NMR (270 MHz. CDC^ 5: 1.26 (s,9H); 3.90 (dd, IH); 4.15 (t, IH); 4.77 (m,2H); 5.03 (m, IH); 7.30 (d, 2H); 7.36 (d, 2H); 7.72 (d, IH); 7.79 (d, IH).
(5i^)-3-(4-^Butylphenyl)-5-a2idomethyloxazohdin-2-one may be prepared by the routes described in WA Gregory et al, J.Med.Chem., 1990, 33,2569.
Example 42: (55)-3-f4-MethvlsuIfonyIphenylV5-(imidazoI-l-ylmethyl)oxazolidin-2-one
(5iS)-3-(4-Methylthiophenyl)-5 The intermediate for this compound was prepared as follows:
(5^-3-r4-Methvlthiopheriy1)-5^irnidazol-t-v1rnethvlloxazolidin--2-one Sodium hydride (80% in oil, 23 mg, 0.77 mM) was stirred under nitrogen in iV^-dimethylformamide (5 ml), imidazole (52 mg, 0.77 mM) added, and stirring continued

for 10 minutes. (5J?)-3-(4-Methyl1mophenyl)-5-memanesulfonyloxymethyloxazolidm-2-one (200 mg, 0.63 mM) was dissolved in JV^dimethylformamide (5 ml), added to the above, and the mixture stirred 18 hours at ambient temperature. After diluting with water (30 ml), the mixture was extracted with ethyl acetate (30 ml), the extract washed with brine (25 ml), dried (magnesium sulfate) and evaporated. The residue was triturated with diethyl ether, and filtered to give the desired product (129 mg, mp 129-131 °). MS (CI): 290(MHr)forC14H15N3O2S
NTvnm70MHz.CDC13;> S: 2.48 (s, 3H); 3.66(dd,lH); 4.11 (t, 1H); 4.28 (dd, 1H); 4.37 (dd, 1H); 4.91 (m, 1H); 7.11 (brs,2H); 7.25 (d,2H); 7.35 (d,2H); 7.58 (brs, IE).
(5i?)-3-(4-Methylthiophenyl)-5-memaaesulfonyloxymethyloxazoHdin-2~one may be prepared from the corresponding 5-hydroxymethyl compound (described by WA Gregory et al, J.Med.Chem., 1989, 32,1673) by a route analogous to that used for the methanesulfonyl intermediate of Example 1.
Example 43: (5^)-3-(4-MethvIthiophenvn-5-fpvra7:n^l-vlmethvnoxazolidiii-2-one
Sodium hydride (80% in oil, 63 mg, 2.1 mM) was stirred under nitrogen in
A^-dimethylformamide (2 ml), (Ji?)-3-(4-methylthiophenyl)-5-methanesulfonyloxymethyl-
oxazolidin-2-one (630 mg, 2 mM) dissolved in A^dimethylformamide (10 ml) added,
followed by pyrazole (140 mg, 2 mM) dissolved in iV^-dimethylformamide (2 ml). Stirring
was continued for 1.5 hours at ambient temperature. After diluting with water (30 ml) and
stirring for 1 hour, the precipitate was filtered to give the desired product (190 mg, mp
72-73°).
VISfEn: 289 (W) for C14H15N302S
WTO (9.70 MHz. fDCI^ 8: 2.47 (s, 3H); 3.96-4.10 (m,2H); 4.50 (d,2H); 4.99 (m, 1H);
>.29 (m, 1H); 7.26 (d, 2H); 7.36 (d, 2H); 7.53 (m, 2H).
Sample 44: r5J?V3-f3.5-Difluoro-4-f3.6-dihvdrn-171 -dioxn-2y7'-thiopvTan-4-ynphenvn-
UT.2.3-triazol-l-vlmethvnoxazo]idiD-2-nnft3Tid(^gUW3.5-Difluoro-4-0.6-dihvdro-l.l-
linvn-2?T-thiopyran-4-vnphenyIV5-fl.2.3-tria7nl-2-ylmethvnnxazolidin^2-oiie
iodium hydride (50% in oil, 72 mg, 1.5 mM) was stirred under nitrogen in

N-Ndrmethylformarnide (3 ml), and a solution of 1,2,3-triazole (104 mg, 1.5 mM) in N,Af-dimemylformamide (4 ml) added, and stirring continued for 10 minutes. (5i?)-3-(3,5-Difluoro-4-(2,6-dihydro-1,1 -dioxo-2^r-thiopyran-4-yl)phenyl)-5-methanesulfonyl-oxymethyloxazolidin-2-one (437 mg, 1 mM) was added as solid, and the reaction heated at 75° for 1.5 hours. The mixture was diluted with aqueous 5% sodium bicarbonate (25 ml), extracted into ethyl acetate (2 x 20 ml), washed with water and brine (20 ml of each), dried (magnesium sulfate) and evaporated. The residue was purified by chromatography on a 10 g i silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 100% ethyl acetate in dichloromethane. Relevant fractions were combined to give the 2-triazole as
the less polar product (250 mg) and the 1-triazole as the more polar product (100 mg).
2-Triazole:
MS (ESP): 411 (MB*) for C17H16F2N404S
NMR (DMSO-d^ 6: 2.82 (m,2H); 3.32 (m overlapped by H20,~2H); 3.90 (dd overlapped
by m, 3H); 4.23 (t, 1H); 4.86 (m, 2H); 5.22 (m, 1H); 5.74 (t, 1H); 7.28 (d, 2H); 7.83 (s,
23).
l-Triazole:
MS (ESP): 411 (MH4) for C17H16F2N404S
NMR (pMSO-dfll 5: 2.82 (m, 2H); 3.32 (m overlapped by H20, ~2H); 3.90 (dd overlapped
bym, 3H); 4.21 (t, 1H); 4.82 (m, 2H); 5.16 (m, 1H); 5.75 (t, 1H); 7.30 (d, 2H); 7.87 (d,
1H); 8.18 (d,lH).
The intermediates for this compound were prepared as follows:
4-(4-Ammo-2.6-difluorQ-phenylVtetrahydro-thiopyran-4-ol
3,5-Difluoroaniline (12.9 g, 0.1 M) in dry tetrahydrofuran (400 ml) was stirred and cooled under nitrogen to -78°. w-Butyllithium (1.6M in hexanes, 131 ml, 0.21 M) was run in slowly over 15 minutes, mamtaining the temperature below -65°. Stirring was continued at the same temperature for 30 minutes, then trimethylsilyl chloride (22.8 g, 0.21 M) in tetrahydrofuran (100 ml) was added dropwise over 15 minutes. The temperature was then allowed to rise to ambient, and the mixture stirred overnight After recooling to -78°, further rc-butylKthium (1.6M in hexanes, 68.8 ml, 0.11 M) was added dropwise below -70°, and stirring continued

for 5 hours to form anion. A solution of tetrahydrothiopyran-4-one (12.5 g, 0.107 M) in tetrahydrofuran (80 ml) was added dropwise, keeping the temperature below -70°, and the temperature allowed to warm to ambient overnight. The mixture was cooled in an ice-bath and acidified to pH NMR (CDCl^ 5: 2.27 (d,2H); 2.40 (t,4H); 2.65 (t, 1H); 3.27 (t,2H); 3.82(brs,2H); 6.17 (d, 2H).
4- 4-(4-Ammo-2,6-d^fluoro-phenyl)-tetrahydro-tMopyran-4-61 (16.7 g, 68 mM) was suspended in a mixture of concentrated hydrochloric acid (200 ml), water (50 ml) and acetic acid (200 ml), BHT (50 mg) added, and the whole stirred under nitrogen at 80° for 18 hours. After cooling, the mixture was made basic by cautious addition of concentrated ammonia, and ice-water. The mixture was then extracted with diethyl ether (2 x 300 ml), the extracts washed with water (100 ml), brine (200 ml) and dried (magnesium sulfate). Evaporation gave the desired product as a cream solid (15.2 g). MS fESP;>: 244 (MlT) for CnHuF2NS
NMR (CDCl^ 5: 2.48 (m,2H); 2.82 (t,2H); 3.30 (m,2H); 3.80 (br s, 2H); 5.87 (s, 1H); 6.17 (d, 2H).
4-r4-Benzyloxycarbony1flrnirio-?..6-difluorophenvD-5.6-dihydro-2g-thiopvran 4-(4-Aiiu^o-2,6-difluorophenyl)-5,6-dihydro-2fl"-thiopyran (15.0 g, 66 mM) was dissolved in dry dichloromethane (250 ml), pyridine (9.45 g, 113 mM) added, and the whole stirred under nitrogen at -20°. Benzyl chloroformate (17.1 g, 100 mM) in dry dichloromethane (25 ml) was added dropwise, and the mixture allowed to warm to ambient over 18 hours. The mixture was

washed with hydrochloric acid (1M, 2 x 200 ml), then brine (200 ml) and dried (magnesium
sulfate). Evaporation to a small volume and dilution with isohexane gave the desired product
as a white solid (22.5 g).
MS (ESP): 362 (MH+) for C19H17F2N02S
NMR (DMSO-dfi) 5: 2.38 (m, 2H); 2.78 (t, 2H); 3.24 (m, 2H); 5.15 (s, 2H); 5.89 (s, 1H);
7.17 (d, 2H); 7.38 (m, 5H); 10.18 (s, 1H).
f5J?V3^3.5»Difluoro^-(2.6-dihvdro-2^-thiopwan-4-vDphenvlV5-hvdroxvmethvloxazo1idin-2-one
4-(4-Benzyloxycarbonylamino-2,6-difluorophenyl)-5,6-dihydro-2iy-thiopyran (22 g, 61 mM) was dissolved in dry tetrahydrofuran (235 ml), stirred under nitrogen, and cooled to -78°. n-Butyllitibium (1.6M in hexanes, 38.2 ml, 0.61 mM) was run in slowly over 20 minutes, mamtaining the temperature below -65°. Stirring was continued at the same temperature for 10 minutes, then (R)-glycidyl butyrate (8.8 g, 61 mM) in tetrahydrofuran (15 ml) was added dropwise over 10 minutes, maintaining the temperature below -60°. The temperature was then allowed to rise to ambient, and the mixture stirred overnight. Methanol (25 ml) was added, and stirring continued for 10 minute, before the addition of aqueous sodium bicarbonate (5%, 200 ml) and extraction with ethyl acetate (400 ml). After washing with sodium bicarbonate (5%, 100 ml), then brine (100 ml) and drying (magnesium sulfate), the solution was evaporated, the residue redissolved in dichloromethane, and product precipitated with isohexane. Recrystallisation from isopropanol gave the desired product (16.2 g). MS fESPV- 328 (MIT) for C35HI5F2N03S
NMR fDMSO-d^ 8: 2.39 (m,2H); 2.80 (t,2H); 3.27 (m,2H); 3.53 (m, 1H); 3.66 (m, 1H); 3.81 (dd, 1H); 4.07 (t, 1H); 4.69 (m, 1H); 5.21 (t, 1H); 5.93 (s, 1H); 7.33 (d, 2H).
r5i?V3-r3.5-Difluoro-4-(2.6-dihydro-l.l-dinxo-2^thinpvran-4-yl)phenyl)-5-hvdroxvmethyl-
oxazolidin-2-one
(JJ?)-3 2-one (6.54 g, 20 mM) was dissolved in dichloromethane (250 ml), and stirred at ambient
temperature. 3-ChJoroperoxy-benzoic acid (80%, 10 g, 46 mM) dissolved in dichloromethane
(90 ml) was added dropwise, and stirring continued for 1 hour. Excess aqueous sodium

metabisulfite was added, and stirring continued for 10 minutes. Excess dichloromethane (~1.5- L) was added to dissolve all organics, and the organic phase separated. After washing ' with aqueous sodium bicarbonate (200 ml) and drying (magnesium sulfate), the filtrate was evaporated to a small volume, and the desired product filtered (6.5 g). MS (ESP): 360 (MH+) for C15H15F2N05S
NMRrDMSO-d£) 5: 2.82 (m, 2H); 3.34 (m overlapped by H20,2H); 3.52 (m, IH); 3.67 (m, IH); 3.83 (dd, IH); 3.91 (m, 2H); 4.08 (t, IH); 4.82 (m, IH); 5.22 (t, IH); 5.83 (t, IH); 7.38 (d, 2H).
(5igV3-r3.5-Difluoro-4-(2.6-dihvdrn-lJ-dioyn-2^-thiopvran^vnphenyn-5-methane~
sulfonyloxymethyloxazolidin-2-one
(5i0-3-(3,5-Difluoro~4-(2,6-dmydro-1,1-dioxo-2^
oxazolidin-2-one (6.1 g, 17 mM) was dissolved in dry tetrahydrofuran (400 ml), and stirred
under nitrogen in an ice-bath. Triethylamine (2.4 g, 23.7 mM) was added, followed by
dropwise addition of methanesulfonyl chloride (2.33 g, 20.3 mM). After stirring for 2 hours
at 0°, the mixture was diluted with aqueous sodium bicarbonate (400 ml) and tetrahydrofuran
evaporated from the mixture. The residue was extracted with dichloromethane (2 x 500 ml),
the extract dried (magnesium sulfate). After evaporation of the filtrate to a small volume, it
was diluted with isohoxane to precipitate the desired product filtered (8.0 g).
MS_(ES£): 438 (MH*) for C16H17F2N07S2
NMR (DMSO-d^ 8: 2.82 (m,2H); 3.25 (s, 3H); 3.33 (m overlapped by H20,~2H); 3.84
(dd, IH); 3.93 (m, 2H); 4.19 (t, IH); 4.48 (m, 2H); 5.03 (m, IH); 5.85 (s, IH); 7.38 (d,
2H).
Example 45: r5i?V3-f;4^ri-Ben2vI-1.2.5.6-tetrahydropvridm-4-vIV3-fluorophepyIV5-(1.2.3"triazoI-l-yImethynoxazolidin-2-one
(5i?)-3-(4-(l-Ben2yl-l,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-azidomethyl-oxazolidin-2-one (4.55 g, 11.2 mM) and norbomadiene (5.15 g, 56 mM) were dissolved in dioxan (50 ml) and heated under reflux for 4 hours. The reaction mixture was evaporated and the product isolated by MPLC on silica, eluting with 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product as a gum which

crystallised on trituration with diethyl ether (2.9 g).
MS (ESP): 434 (MH4) for C24H24FN502
NMRrDMSO-dg) 5: 2.43 (s, 2H); 2.63 (t, 2H); 3.04 (d, 2H); 3.69 (s, 2H); 3.89 (dd, 1H);
4.24 (t,lH); 4.84 (d,2H); 5.14 (m,lH); 5.98 (s, 1H); 7.32 (m, 8H); 7.75 (s, 1H); 8.15 (s,
1H).
The intermediates for this compound were prepared as follows:
r57?)-3-r4-(l-Benzyl-1.2.5.6-tetrahvdropvridin-4-yl)-3-fluorophenyD-5-methanesulfonvl-
oxymethvloxazolidin-2-one
(5ii)-3-(4-(l-Benzyl-l,2,5,6-tetrahydropyridm^^
oxazolidin-2-one (4.97 g, 13 mM; WO 97-30995) was reacted by essentially the technique of
the related intermediate of Example 1, to give the desired product without chromatography
after trituration with diethyl ether (5.78 g).
MS (ESP): 461 (MH*) for C^FNAS
NMRfDMSO-d^ 5: 2.43 (s,2H); 2.62 (t,2H); 3.03 (d,2H); 3.25 (s, 3H); 3.58 (s,2H);
3.84 (dd, 1H); 4.18 (t, 1H); 4.47 (m, 2H); 5.02 (m, 1H); 5.98 (s, 1EQ; 7.32 (m, EH).
r5J?)-3-r4-ri-Ben2rvl-lr2.5.6-tetrahydropvridin-4-yIV3-fluorophenyl)-5-azidomethyl-
oxazolidin-2-one
(5i?)-3-(4-(l-Benzyl-l,2,5,6-tetrahydropyridm-4-yl)-3-fluorophenyl)-5-memanesm,fonyl-
oxymethyloxazolidin-2-one (5.61 g, 12.2 mM) was reacted by essentially the technique of the
related intermediate of Example 1, except that dimethylsulfoxide was used as solvent, to give
the desired product (4.66 g).
MS (ESP): 408 (MET) for C2ZH22FN502
NMRfDMSO-d^ 8: 2.45 (s, 2H); 2.62 (t, 2H); 3.05 (d, 2H); 3.56 (s, 2H); 3.71 (m, 3H);
4.15 (t, 1H); 4.88 (m, 1H); 5.95 (s, 1H); 7.31 (m, 8H).

Example 46: f5gV3-(4-fl .2.5.6-tetrahvdropvridiii-4-yn-3-fliiorophen vlVS-fl ,2.3-triazol-l-vlmethynoxazoIidin-2-nne
(5iO-3 ylmethyl)oxazolidin-2-one (2.75 g, 6.35 mM) and A^/^-diisopropylethylamine (165 mg, 1.27 mM) in dichloromethane (30 ml) at 0-4° under nitrogen were treated dropwise with 1-chloroethyl chloroformate (1.09 g, 7.62 mM). The solution was stirred for 30 minutes, then evaporated. The residue was purified by MPLC on silica, eluting with a gradient from 0-20% acetonitrile in ethyl acetate, to give the intermediate carbamate as a crystalline solid. This was heated under reflux in methanol (50 ml) for 20 minutes. Evaporation of the solvent and trituration with ethyl acetate gave the desired product as its hydrochloride salt (1.94 g). MS (ESP): 344(MEr)forC17H18FN502
NMRfDMSO-dfi) 8: 2.63 (s, 2H); 3.24 (2d, 2H); 3.72 (d, 2H); 3.92 (m, IH); 4.23 (t, IH); 4.83 (d, 2H); 5.15 (rn, IH); 6.03 (s, IH); 7.29 (dd, IH); 7.42 (m, 2H); 7.76 (s, IH); 8.17 (s, IH); 9.24 (s,2H); +1H for HC1 salt.
Example 47: (5K)-%44-fl -Formvl-1.2.5.6-tetrahvdropyridin-4-vlV3-fliiorophenyn-5-r1.2.3-triazol-l-ylmethyI)oxazolidin-2-one
;5i?)-3-(4-(l,2,5,6-Tetrahydropyria^4-yl)-3-fluorophenyl)-5-(l,2,3-triazol-l-ylme
3xazolidin-2-one hydrochloride (450 mg, 1.19 mM) and triemylarnine (156 mg, 1.56 mM)
vere heated under reflux for 48 hours in ethyl formate (20 ml). The reaction mixture was
liluted with ethyl acetate (30 ml) and washed with water and brine. Drying (sodium sulfate)
ind evaporation gave a gum which crystallised on trituration with diethyl ether to give the
lesired product (358 mg).
vlS (ESP): 372(MH+)forClgHJ8FN503
■JMR (DMSO-d^ 5: 2.38 (br, 2H); 3.59 (m, 2H); 3.91 (dd, IH); 4.06 (dd, 2H); 4.22 (t,
H); 4.83 (d, 2H); 5.13 (m, IH); 6.00 (2 x s, IH); 7.23 (dd, IH); 7.38 (m, 2H); 7.75 (s,
H); 8.14 (2 xs, IH); 8.17 (s, IH).

Example 48: f5/gV3-r4-(l-Benzyl-1.2.5.6-tetrahydropyridm-4-vn-3.5-difluoropheiivn-S-fl.2.3-triazo]-l-v]methvno\azolidm-2-one
(5i?)-3-(4-(l-Berizyl-l,2,5J64etrahydropyridm-4-yl)-3,5-oMuorophenyl)-5-azidometb.yl-
oxazolidin-2-one (850 mg, 2 mM) was reacted by essentially the teclmique of Example 45, to
give the desired product (550 mg).
MS (ESP): 452 (MET) for C24H23F2N502
NMRfDMSO-d^ 5: 2.29 (s, 2H); 2.61 (t, 2H); 3.05 (s, 2H); 3.59 (s, 2H); 3.88 (dd, IH);
4.21 (t, IH); 4.80 (d, 2H); 5.15 (m, IH); 5.78 (s, IH); 7.29 (m, 7H); 7.75 (s, IH); 8.15 (s,
IH).
The intermediates for this compound were prepared as follows:
f5JgV3-f4-n-Beri7^1-1.2.5.6-tetrahydropyridm^
oxymethyloxazolidm-2-one
(5i?)-3-(4"(l-Benzyl-l,2s5J64etrahydropyriaUn-4-yl)-3,5-diiluorophenyl)-5-hydroxymemy^
oxazolidin-2-one (WO 99-64417; 8.4 g, 21 mM) was reacted by essentially the technique of
the related intermediate of Example 1, to give the desired product without chromatography
after trituration with diethyl ether (9.38 g).
NMR(DMSO-d^ 8: 2.30 (s, 2H); 2.62 (t, 2H); 3.05 (d, 2H); 3.24 (s, 3H); 3.58 (s, 2H);
3.82 (dd, IH); 4.17 (t, IH); 4.46 (m, 2H); 5.02 (br s, IH); 5.78 (s, IH); 7.30 (m, 7H).
(5J?)-3-r4-(l-Ben2yl-1.2.5.6-tetrabvdrop\nidin-4-ylV3.5-difiuoropheny1)-5-azidomethvl-
nxazolidm-2-one
(5it)-3-(4-(l-Beoi2yl-l,2J5,6-te1xahydropyridm-4-yl)-3,5-drfluorophenyl)-5-methanesulfonyl-
Dxymethyloxazolidin-2-one (4.06 g, 8.5 mM) was reacted by essentially the technique of the
related intermediate of Example 1, except that dimethylsulfoxide was used as solvent. After
work-up, the residue was purified by MPLC on silica, eluting with 50% z'sohexane in ethyl
icetate, to give the desired product as a gum which crystallised on trituration with ethyl
icetate and wohexane (2.84 g).
VTS flBSP): 408 (MH+) for CaE3aiF2NJ02
sJMR rPMSO-df) 6: 2.31 (s,2H); 2.62 (t,2H); 3.05 (d,2H); 3.60 (s,2H); 3.75 (m, 3H);

4.12 (t, IH); 4.90 (m, IH); 5.88 (s, IH); 7.30 (m, 7H).
Example 49: r5JZV3-f4-(1.2.5.6-tetrahvdropyridm-4-vIV3.5-difluorophenvlV5-a.2.3-triazol-l-ylmethyDoxazoIidin-2-nne
(5i?)-3-(4 ylmethyl)oxazoridin-2-one (1.13 g, 2.5 mM) was reacted by essentially the technique of
Example 46, to give the desired product as its hydrochloride salt (665 mg).
MS (ESP): 362 (MET) for C17H17F2N502
NMR fDMSO-d;> 8: 2.55 (overlapping DMSO, ~2H); 3.29 (overlapping H20, ~2H); 3.79
(d52H); 3.90(dd,lH); 4.23 (t, IH); 4.82 (d,2H); 5.19 (m, IH); 5.90 (s, IH); 7.31 (d,2H);
7.76 (s,lH); 8.18 (s, IH); 9.25 (s,2H); +1H for HC1 salt
Example 50: r5/?V3-(4-a-Formvl-1.2.5.6-tetrahydropyridin-4-vn-3.5-difluorophenvn-5-(lf2f3-triazol--l-y]methyI)oxazolidin-2-one
(5J?)-3-(4-(l,2,5,6-Tetrahydropyridm^-yl)-355-difiuorophenyl)-5-(l,2,3-tria2ol4
oxazolidin-2-one hydrochloride (450 mg, 1.13 mM) was reacted by essentially the technique
of Example 47, to give the desired product (387 mg).
MS (ESP): 390 (MPT) for C18H17F2N503
NMRrDMSO-d^ 5: 2.33 (2 x s, 2H); 3.60 (m,2H); 3.90 (dd, IH); 4.05 (2 x d, 2H); 4.23
(t, IH); 4.82 (d, 2H); 5.18 (m, IH); 5.90 (2 x s, IH); 7.28 (d, 2H); 7.75 (s, IH); 8.13 (2 x s,
IH); 8.16(2xs,lH).
Example 51: r5flV3-(4-(;i>(2-AcetoxyacetyIV1.2.5.6-tetrahydropvridin-4-yn-3.5-difluoro-phenyl)-5-(1.2.3-triazol-l-ylmethyI)oxazolidin-2-one
A solution of (5i?)-3-(4-(l,2,5,6-tetrahydropyridin-4-yl)-3,5-difluorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazolidin-2-one hydrochloride (650 mg, 1.64 mM) in acetone (20 ml) and water (10 ml), was treated with sodium bicarbonate (1.38 g, 16.4 mM) and the mixture cooled to 0-4°. Acetoxyacetyl chloride (448 mg, 3.28 mM) was added dropwise and the reaction mixture stirred at 0-4° for 20 minutes before allowing to warm to ambient temperature. After dilution with water the mixture was extracted well with ethyl acetate. The organic phase was separated, dried (sodium sulfate), solvent evaporated, and the residue triturated with diethyl

ether to give the desired product (702 mg).
MSiESE}: 462 (MET) for G21H2IF2N505
NMR (DMSO-d^ 8: 2.09 (s, 3H); 2.36 (2 x s, 2H); 3.60 (m,2H); 3.89 (dd, IH); 4.09 (br,
2H); 4.23 (t, IH); 4.83 (m, 4H); 5.18 (m, IH); 5.89 (s, IH); 7.29 (d, 2H); 7.78 (s, IH);
8.20 (s} IH).
Example 52: fr5/?V3-r4-(l-r2~Hvdro]cyacetyn-1.2.5.6-tetrahydropvridin-4-vn-3.5-diflnorophenyI)-5-(1.2T3-triazol-l-ylmethyI)oxazoIidin-2-one
(5i?)-3 NMRfDMSO-d^ 5: 2.32 (2 x s, 2H); 3.54 (br, IH); 3.68 (br, IH); 3.99 (dd, IH); 4.10 (m, 4H); 4.24 (t, IH); 4.58 (m, IH); 4.82 (d, 2H); 5.18 (m, IH); 5.88 (br, IH); 7.28 (d, 2H); 7.77 (sslH); 8.17 (s, IH).
BTrample 53: (5flV3-f4-f Wf4SV2.2-dimethvl-l .3-dioxoIane-4-carbonvIVI .2.^.6-tetrahydropyridin-4-yl)"3.5-dijHuorophenyI)-5-(lr2.3-triazol-l-ylmethyI)oxazoIidin-2-one
A. solution of (Ji?)-3-(4-(l,2,5,6.terrahydropyridm^-yl)-3,5-difluorophenyl)-5-(l,2,3-triazol-L-yhnethyl)oxazolidin-2-one hydrochloride (650 mg, 1.64 mM) in dry dichloromethane (20 nl) at 0-4°, was treated with pyridine (648 mg, 8.2 mM) followed by dropwise addition of y1S)-2,2-dimethyl-l,3-dioxolane-4-carbonyl chloride (430 mg, 2.64 mM). The solution was allowed to warm to ambient temperature and stir for 1 hour. The reaction mixture was washed with water and brine, dried (sodium sulfate) and evaporated to a gum which crystallised readily on trituration with diethyl ether to give the title compound (788 mg). MS (ESP): 490 (ME") for C^H^NA
NMR 8: 1.32 (d, 6H); 2.34 (2x s, 2H); 3.87 (dd, IH); 4.09 (t, IH); 4.20 (t, 2H); 3.00-4.30 (m, 4H); 4.80 (d, 2H); 4.90 (m, IH); 5.15 (m, IH); 5.89 (s, IH); 7.25 (d, 2H); 7.75 (s, IH); 8.17 (s, IH).

Example 54: f5Jr>-344-fWf2^-2.3-Dihvdroxvpropionvr>-1.2.5.6-tetrahvdropvHdin-4-ylV3.5-difloorophenvIVS-ri.2.3-triazoI-l-vImetliynoxazolidin-2-one
To a stirred solution of (5i2)-3-(4-(l-((4S)-2,2-dime^
tetrahydropyridm-4-yl)-3,5-difluorophen
mg, 1.43 mM) in tetrahydrofuran (25 ml) was added aqueous hydrochloric acid (1M, 15 ml)
and the mixture stirred at ambient temperature for 2 days. Solvent was evaporated and the
residue treated with water (10 ml). Aqueous sodium acetate (10%, 10 ml) was added, and the
precipitate filtered and washed with ethanol and diethyl ether to give the title compound (514
mg).
MS (ESP): 450 (MET) for C20H21F2N5O5
NMRfDMSO-dg) 6: 2.33 (m, 2H); 3.51 (m, 3H); 3.71 (br, 2H); 3.90 (dd, 1H); 4.00-4.40
(complex, 3H); 4.67 (m, 1H); 4.82 (d,2H); 4.92 (m,lH); 5.15 (m,lH); 5.87 (s,lH); 7.27
(d, 2EQ; 7.76 (s, 1H); 8.17 (s, 1H).
Example 55: (5ff>3-(4-fl -^-AcetoxyacetylVI .2.5.6-tetrahydropyridin-4-ylV3-fIuoro-phenyfl-5-fl .2.3-triazol-l -ylmeth vftoxazoIidm-2-one
(Jie)-3-(4 oxazolidin-2-one hydrochloride (803 mg, 2.11 mM) was reacted by essentially the technique
of Example 51, to give the desired product (767 mg).
MS (ESP): 444 (MH*) for CI1H22FN5Os
NMR (DMSO-dg) 8: 2.00 (s, 3H); 2.41 (s, 2H);. 3.59 (m, 2H); 3.90 (dd, 1H); 409 (s, 2H);
4.25 (t, 1H); 4.83 (m, 4H); 5.15 (m, 1H); 5.98 (s, 1H); 7.25 (dd, 1H); 7.40 (m, 2H); 7.76
(s, 1H); 8.17 (s, 1H).
Example 56: f5J?V3-f4-n-(2-HydroxyacetvlV1.2.5.6-tetrahydropvridin-4-yi;>-3-flnoro-phenvn-5-a.2.3-triazoI-l-yImethynoxazolidin-2-one
(5if)-3-(4 triazoM-ylmethyl)oxazolidin-2-one (443 mg, J mM) was reacted by essentially the technique
of Example 51, to give the desired product (370 mg).
MS (ESP): 402(MH4)forC19H20FNsO4
KMR (DMSO-d;> 5: 2.45 (s, 2H); 3.60 (m, 2H); 3.89 (dd, 1H); 4.12 (m, 4H); 4.25 (t, 1H);

4.55 (m, 1H); 4.82 (d, 2H); 5.15 (m, 1H); 6.00 (d, 1H); 7.25 (dd, 1H); 7.40 (m, 2H); 7.75 (s, 1H); 8.16 (s, 1H).
Example 57: (5K)-3-(4-(l-((4S)-2.2-dimethy\A .3-dioxo]ane-4-cai'bonylVl,2.5.6-tetrahvdropyridm-4-ylV3-flnorophenyIV5-n.2.3-triazol-l-vImethvDoxazolidin-2"Qne
(5J0-M4-(l,2,5,6-Tetrahydropyridm-4-yl)-3-fl^^
oxazolidin-2-one hydrochloride (651 mg, 1.71 mM) was reacted by essentially the technique
of Example 53, to give the desired product (697 mg).
MS fESPV 472 (MIT) for C^H^FNA
NMR toMSO-d^ 8: 1.31 (m, 6H); 2.40 (s, 2H); 3.60-4.30 (complex, 8H); 4.83 (d, 2H);
4.90 (m, 1H); 5.15 (m, 1H); 6.00 (s, 1H); 7.15 (dd, 1H); 7.40 (m, 2H); 7.73 (s, 1H); 8.15
(s, 1H).
Example 58: r5i?V3--r4-fl-ra (5£)-3 fluorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazoHdm-2-one (600 mg, 1.27 mM) was reacted
by essentially the technique of Example 54, to give the desired product (443 mg).
MS fESPI: 432 (MH*) for C^FNA
NMR.rDMSO-d,') 8: 2.40(br,2H); 3.35-3.85 (complex, 4H); 3.90(dd,lH); 4.10 (s,lH);
4.25 (t, 2H); 4.35 (m, 1H); 4.65 (m, 1H); 4.82 (d, 2H); 4.93 (m, 1H); 5.13 (m, 1H); 6.00
(s, 1H); 7.22 (dd, 1H); 7.38 (m, 2H); 7.73 (s, 1H); 8.15 (s, 1H)
Example 59: r5JgV3-r4-ri-BRTizvI-1.2^.fi-tetrahvdropvridin-4-yIV3.5-difliinrophenvn-5-fl^.g-triazoI^-vimethvDoxazoIidin^-one
(5i?)-3-(4-(l-B erizyl-1,2,5,6-tetrahydrop v^^
oxymethyloxazolidm-2-one (2.39 g, 5.0 mM) was dissolved in A^dimemylfonnamide (25 ml), and treated with 1,2,3-triazole (690 mg, 10 mM) and anhydrous potassium carbonate (1.3 8 g, 10 mM), then stirred at 80° for 3 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, brine, dried (magnesium sulfate) and evaporated to a gum, which was purified by MPLC on silica, eluting

with a gradient from 10 to 100% ethyl acetate in isohexane. Combination, of appropriate fractions gave two products as gums which crystallised on trituration with, diethyl ether. The less polar product was identified as the desired product (1.45 g). MS (ESP): 452 (MH+) for C^H^NA
NMRtoMSO-d£) 5: 2.31(s,2H); 2.62 (t,2H); 3.05 (d,2H); 3.59 (s,2H); 3.89(dd,lH); 4.21 (t, IH); 4.83 (m, 2H); 5.21 (m, IH); 5.78 (s, IH); 7.27 (m, 7H); 7.82 (s, 2H). The more polar product (760 mg) was identified as the 1-substituted triazole isomer of Example 48.
Example 60: (SffWU4-(1 -Benzvl-1.2.5.6-tetrahydropvridm-4-yn-3.5-difluorophenvIV5-Q.2.4-triazoI-l-ylmethynnxaznlidm-2-one
(5i?)-3-(4-(l-Benzyl-l,2,5s6-tetrahyd^opvridm-4-yl)-3,5-difluorophenyl)-5-memanesu^ oxymethyloxazolidin-2-one (956 mg, 2.0 mM) was dissolved in TV^V-dimethylformamide (12 ml), treated with 1,2,4-triazole (173 mg, 2.5 mM) and anhydrous potassium carbonate (690 mg, 5.0 mM) and stirred at 80° for 18 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, brine, dried (magnesium sulfate) and evaporated to a gum which was purified by MPLC on silica eluting with a gradient from 0 to 20% acetonitrile in ethyl acetate. Evaporation of appropriate fractions gave the title compound (719 mg) after trituration with diethyl ether. M&JBSE): 452(MH0toCMHaFaN5O2
NMR(DMSO-d£) 5: 2.30 (s,2H); 2.61 (s,2H); 3.05 (d,2H); 3.69 (s,2H); 3.80 (do, IH); 4.20 (t, IH); 4.60 (m, 2H); 5.09 (m, IH); 5.80 (s, IH); 7.30 (m, 7H); 6.99 (s, IH); 8.56 (s, IH).
Example 61: (5RV3-(4~Cl .2.5.6-Tetrahydropyridm^-vIV3.5-diflaorophenylV5-Q.2.4-triazol-l-vlmethyl)oxazolidiii-2-one
(5i?)-3 /lmethyl)oxazolidin-2-one one (631 mg, 1.4 mM) was reacted by essentially the technique of
Example 46, to give the desired product as its hydrochloride salt (401 mg).
VtS (ESP): 362 (MHO for C17H17F2N502
^VTR fDMSO-dJ 5: 2.55 (overlapping DMSO, ~2H); 3.25 (overlapping H20,~2H); 3.73

(s,2H); 3.9(dd, IH); 4.17 (t, IH); 4.60 (t,2H); 5.10 (m,lH); 5.87 (s, IH); 7.27 (d, 2H); 7.98 (s, IH); 8.55 (s, IH); 9.23 (s, 2H); +1H for HC1 salt
Example 62: f5JgV3-r4-n-rf4iy>-2.2-DimethvM.3-dioYo]ane-4-carbonv1V1.2.^.fi-tetrahydropvridin-4-yn-3.5-difluorophenylV5-n .2.4-triazoI-l -vlmethvnnyazoIidin-2-one
(5i0-M4 oxazolidni-2-one hydrochloride (399 mg, 1.0 mM) was reacted by essentially the technique of
Example 53, except that purification by MPLC on silica eluting with 5% methanol in
dichloromethane was needed, to give the desired product (288 mg). MS (ESP): 490 (MH*)
for CJJH^FJNA
NMR(DMSO-de) 8: 1.32 (d, 6H); 2.35 (m,2H); 3.70 (m, 2H); 3.90(dd,lH); 3.95-4.30.
(complex, 5H); 4.60 (m, 2H); 4.88 (m, IH); 5.10 (m, IH); 5.85 (s, IH); 7.25 (d, 2H); 7.98
(s, IH); 8.55 (s, IH).
Example 63: (5RV3-(4-n -rr2V)-2.3-Dihydroxvpropionvn-1.2.5.6-tetrahvdropvridin-4-yI)-3.5-diflnorophenyIV5-(1.2.4-triazoI-l-ylmethyl)oxazoHdiii-2-one
(5i?)-3-(4-(l-((^,S)-2,2-Dimemyl-l,3-dioxolane-4-carbonyl)-l,2,5,64etrahydropyridm-4-yl)-3,5-difluorophenyl)-5-(l,2,4-triazol-l-y]methyl)oxazolidin-2-one (269 mg, 0.55 mM) was reacted by essentially the technique of Example 54, to give the desired product (130 mg). MS (ESP): 450 (MH+) for C^F^C^
NMR rDMSO-d^ 6: 2.35 (m,2H); 3.52 (m,2H); 3.72 (br,2H); 3.92 (dd, IH); 4.00-4.45 (complex, 4H); 4.65 (m, 3H); 4.98 (m, IH); 5.15 (m, IH); 5.90 (s, IH); 7.30 (d,2H); 8.00 (s, IH); 8.55 (s, IH).
Example 64: (5J?)-3-(4-(1 -rf2J?V2-Hvdroxy-3-methylthiopropionvn-1.2.5.6-tetrahvdropvridin-4-yn-3-flTiorophenyl)-5-a.2.3-triazol-1-ylmethyI)oxazolidin-2-one
(5i?)-3-(4-(l,2,5,6-Tetrahydropyridm-4-yl-3-fiuorophenyl)-5-(l,2,3-triazol-l-ylmethyl)-oxazohdin-2-one hydrochloride (400 mg, 1.05 mM), (2J2)-2-hydroxy-3-methylthiopropionic acid (143 mg, 1.05 mM; WO 92-00276), l~hydroxybenzotriazole (184 mg, 1.37 mM) and A^A^-diisopropylemylamine (177 mg, 1.37 mM) were dissolved in dichloromethane (10 ml) and l-(3-dimemylammopropyl)-3-emylcarbodiimide hydrochloride (263 mg, 1.37 mM) was

added portionwise, and the mixture was stirred overnight. Solvent was removed and crude product purified by flash chromatography on silica eluting with 2% methanol in dichloromethane, to afford the title compound as a clear oil that readily crystallised (480 mg). MSJ£S£): 462(MH^forC2IH24FN504S
NMRtoMSO-d^ 8: 2.10 (s, 3H); 2.43 (m, 2H); 2.61 (m, IH); 2.78 (m, IH); 3.65 (m, 2H); 3.90 (m, IH); 4.17 (m, 2H); 4.24 (t, IH); 4.50 (m, IH); 4.84 (d, 2H); 5.15 (m, IH); 5.44 (dd, IH); 6.03 (s, IH); 7.20-7.45 (m, 3H); 7.77 (s, IH); 8.17 s, IH).
Example 65: (5R)-3-(4-(l -^J?)-2-Hvdroxy-3-methanesuIfonvIpropionyn-1.2.5.6-tetrahvdropyridin-4-vn-3-flnornphenvIV5-fl.2.3-triazoI-l-ylmethynoxazolidiii-2-one
(5iO-3-(4-(l-((2i2)-2-Hydroxy-3-memylth^
fluorophenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazoUdin-2-one (430 mg, 0.93 mM) was stirred in dichloromethane (15 ml) at 0°, and 3-chloroperoxybenzoic acid (70%, 456 mg, 1.87 mM) was added portionwise. The solution was stirred at 0° for 1 hour. Dichloromethane (50 ml) was added and the mixture washed with saturated aqueous sodium bicarbonate (50 ml), dried (magnesium sulfate) and evaporated. Crude product was purified by flash chromatography on silica eluting with 4% methanol in dichloromethane to give the title compound as a white solid (349 mg).
MS rBSP): 494 (MH4) for C21H24FN506S
NMR fDMSO-d^ 6: 2.18-4.23 (m, 8H); 3.03 (s, 3H); 3.92 (m, IH); 4.23 (t, IH); 4.78 (m, IH); 4.83 (d, 2H); 5.14 (m, IH); 6.02 (dd, IH); 6.04 (s, IH); 7.20-7.46 (m, 3H); 7.75 (s, IH); 8.17 (s, IH).
Example 66: (5^-3-r4-a-BenzyI-t.2.5.6-tetrahydropyridiii-4-yn-3-flnorophenyn-5'(2-oxo-3J?">-1.3-oxazol-3-yImethyl)nyazolidin-2-one
(5i?)-3-(4-(l -Benzyl-1,2,5,6-tetrahydropyridin-4-yl)-3 -fluorophenyl>5-hydroxymethyl-oxazolidin-2-one (2.92 g, 7.3 mM; WO 97-30995) was stirred in tetrahydrofuran (60 ml), and 3#-oxazol-2-one (0.69 g, 8.12 mM) and {ributylphosphine (1.77 g, 8.75 mM) were added. The mixture was stirred at 0° under nitrogen, and lsr-azodicarbonyldipiperidme (2.06 g, 8.18 mM) was added portionwise. The reaction mixture was allowed to warm to ambient temperature and stirred overnight. The precipitate was filtered off and solvent removed. The

resulting oil was dissolved in dichloromethane (30 ml), stirred at 0° for 30 minutes, and further precipitate removed. The filtrate was purified by MPLC on silica eluting with a gradient from 60 to 80% ethyl acetate in wohexane, to give a mixture of starting material and product, which was rechromatographed eluting with 3% MeOH in dichloromethane to give the title compound as a white solid (30 mg). MS (ESP): 468 (MET) for QsH^NA
Wm rDMSQ-d^ 5: 2.28 (m, 2H); 2.62 (t, 2H); 3.04 (m, 2H); 3.57 (s, 2H); 3.78-3.95 (m, 3H); 4.17 (t, 1H); 4.96 (m, 1H); 5.78 (s, 1H); 7.07 (d, 1H) 7.19 (d, 1H); 7.21-7.35 (m, 7H).
Example 67: r51y)-3-r4-r3.6-Dihvdro-2g-pvran-4-vIV3-fluorophenvn-5-r2-oyo-1 H-pyridin-l-ylmethyI)oxazolidin-2-one
2-Hydroxypyridine (108 mg, 1.14 mM) was added at room temperature, under an atmosphere of nitrogen, to a stirred suspension of sodium hydride (60% dispersion in oil, 48 mg, 1.2 mM) in Ay^-dimethylformamide (5 ml). The reaction was stirred for 30 minutes then (i/2)-3-(4-(336-dihydro-2^-pyran-4-yl)-3-fluorophenyl)-5-memanesulfonyloxymemyloxazoUdin-2-one (400 mg, 1.08 mM; WO 97-09328) was added in one portion. The mixture was stirred and heated at 60° for 5 hour before quenching in water (20 ml) and extracting with ethyl acetate. The extract was washed twice with water and once with saturated brine, dried (magnesium sulfate) and evaporated to an orange oil, which was purified by flash chromatography on silica, eluting with 2.5% methanol in dichloromethane to give the title compound (115 mg) as a colourless solid.
MS fESP): 371 (MIT) for C10H19FN2O4
NMR (CDC\) 5: 2.50 (m, 2H); 3.90 (m, 3H); 4.15 (t, 1H); 4.22 (dd, 1H); 4.31 (m, 2H); 4.46 (dd, 1H); 5.17 (m, 1H); 6.06 (m, 1H); 6.25 (t, 1H); 6.60 (d, 1H); 7.14 (dd, 1H); 7.26 (t, 1H); 7,30-7.45 (m, 3H).
Example 68: r5igV3-r4-f3.6-Dihvdro-2g-pvran-4-yn-3-fluorophenyn-5-f2-oxo-2Jy-pyridaz-l»yImethyI)oxazolidin-2-one
Diisopropylazodicarboxylate (248 mg, 1.2 mM) was added at room temperature to (5i?)-3-(4-(3,6-dmydro-2iJ-pyran-4-yl)-3-fluorophenyl)-5-hydroxymethyloxazoHdin-2-one(300mg, 1.02 mM), 2#-pyridazin-3-one (118 mg, 1.22 mM) and triphenylphosphine (340 mg, 1.30

mM) in tetrahydrofuran (8 ml). The reaction was stirred for 30 minutes then solvent
evaporated and the residue purified by flash chromatography on silica, eluting with a gradient
from 0 to 10% methanol in ethyl acetate, to give the title compound as a colourless solid (219
mg).
MS : 372 (MH1) for C19H18FN304
NMRfCDCl^ 8: 2.50 (m, 2H); 3.90 (t, 2H); 3.96 (d, IH); 4.12 (t, IH); 4.32 (m, 2H); 4.50
(dd, IH); 4.58 (dd, IH); 5.14 (m, IH); 6.05 (m, IH); 6.96 (dd, IH); 7.17-7.28 (m, 3H);
7.38 (dd, IH); 7.81 (m, IH).
Example 69: C5i?V3-r4-fl-Benzy]-1.2.5.6-tetrahvdropvridiii-4-vn-3-fluorophenvn-5-
(tetrazol-l-ylmethyl)oxazolidin-2-oneand(5J?)-3-f4-(l-Benzyl-1.2.5:.6-tetrahydropyridiii-
4-yfl-3-fluorophenyI)-5-(tetrazol-2-yImethyftoxazoIidin-2-one
Diethylazodicarboxylate (2.28 g, 13.1 mM) was added, under an atmosphere of nitrogen, to a
mixture of (5iZ)-3-(4-(l-benzyl-l,2,5364etrahydropyiidin-4-yl)-3-fluorophenyl)-5-
hydroxymethyloxazoHdin-2-one (5.0 g, 13.1 mM; WO 97-30995), l#-tetrazole (0.91 g, 13.0
mM) and rriphenylphosphine (3.43 g, 13.1 mM) in tetrahydrofuran (150 ml), pre-cooled in
ice/water. The reaction was then allowed to warm to room temperature and stirred 18 hours.
Solvent was evaporated and the resulting brown oil dissolved in dichloromethane (80 ml) and
cooled in ice/water before filtering. The filtered solution was purified by MPLC on silica,
eluting with ethyl acetate to give the title compounds; the 2-tetrazole isomer is the less polar,
and elutes first. Each was then individually purified by strong cation ion-exchange
chromatography (10 g Bond Elut®), elutmg with a gradient from 0 to 5% methanol in
dichloromethane, followed by 3% 880 ammonia in a 9:1 mixture of dichloromethane and
methanol, to give 2-tetrazole (2.61 g) and 1-tetrazole isomers (0.44 g) as colourless solids.
2-Tetrazole:
MS ffiSPl- 435 (MH*) for C^FNA
NMR(DMSO-d^ 6: 2.42 (m, 2H); 2.60 (t, 2H), 3.05 (d, 2H), 3.58 (s, 2H); 3.91 (dd, IH);
4.30 (t, IH); 5.11-5.31 (m, 3H); 5.97 (m, IH); 7.19-7.44 (m, 8H); 9.01 (s, IH).
1-Tetrazole:
MS (ESP): 435 (MH1) for C^FNA
NMR (DMSO-d^ 5: 2.43 (m,2H); 2.60 (t,2H); 3.04 (d, 2H); 3.58 (s,2H); 3.92 (dd, IH);

4.25 (t, IH); 4.93 (d, 2H); 5.17 (m, IH); 5.97 (m, IH); 7.19-7.44 (m, 8H); 9.48 (s, IH).
Example 70: f5J?V3-r4-fl.2.5.6-Tetrahvdropyridin-4-vn-3-fluorophenvn-5-ftetr27n1-2-ylmethvfloxazoIidin-2-one
1-Chloroetbyl chloroformate (1,18 g, 8.3 mM) was added dropwise, under an atmosphere of nitrogen, to a stirred solution of (5i?)-3-(4-(l-ben2yl-l,2,5564etrahydropyridin-4-yl)-3-fluoro-phenyl)-5-(tetrazol-2-ylmethyl)oxazoUdin-2-one (2.56 g, 5.90 mM) and T^TV'-dusopropylemylamine (0.230 mg, 1.77 mM) in dichloromethane (50 ml) with cooling in ice/water. The reaction was stirred for 30 minutes at ice temperature, and the brown solution purified by MPLC on silica, eluting with 75% ethyl acetate in zsohexane. The resulting carbamate intermediate was dissolved in methanol (60 ml) and heated at 60° for 30 minutes. Evaporation of the solvent and trituration with diethyl ether gave the title compound (1.76 g) as its hydrochloride salt. MS fBSP): 345 (MH4) for ClfiH17FN602
NMR fDMSO-d^ 8: 2.65 (s, 2H); 3.28 (t, 2H); 3.72 (d, 2H); 3.92 (dd, IH); 4.30 (t, IH); 5.11-5.32 (m, 3H); 6.03 (m, IH); 7.28 (m, IH); 7.38-7.50 (m, 2H); 9.05 (s, IH); 9.30 (br s; 2H).
Example 71: f5/?KW4-fl-f(4Vl2.2-Dimethvl-1.3-dioxolane-4-carbonvn-1.2.5.6-tetrahydropyridin-4--vlV3-fluorophenvlV5-(tetrazol-2-ylmethvI)oxazoHdip-2-one
(^5)-2,2-Dimethyl-l,3-dioxolane-4-carbonyl chloride (350 mg, 2.10 mM) was added dropwise to a stirred suspension of (5i2)-3-(4-(l,2,5,6-tetrahydropyridin-4-yl)-3-fluoro-phenyl)-5-(tetrazol-2-ylmethyl)oxazolidin-2-one hydrochloride (500 mg, 1.31 mM) and pyridine (0.52 g, 6.57 mM) in dichloromethane (20 ml) with ice/water cooling. The reaction was allowed to warm to room temperature and stirred 1 hour. The resulting solution was washed with water and saturated brine, dried (magnesium sulfate) and evaporated to a small volume. Addition of diethyl ether gave the title compound (600 mg) as a yellow solid. MS (ESP*)'. 473 (MET) for C^H^FNA
NMR (DMSO-

Example 72: f5i?V3-f4-fl-(1-Ac.Ptnxyacetyl)-l.2.5.6-tetrahydropvridm-4-vlV3-flTinrn-phenyIV5-ftetrazoI-2-vImethvI)nxazolidm-2-one
Acetoxyacetyl choride (0.356 mg, 2.63 mM) was added dropwise to a stirred solution of (5R)~ 3-(4-(l,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)-5-(tetrazol-2-ylmethyl)oxa^ hydrochloride (500 mg, 1.31 mM) and sodium hydrogen carbonate (1.10 g, 13.1 mM) in a mixture of water (10 ml) and acetone (20 ml) with ice/water cooling. The reaction was allowed to warm to room temperature and stirred 16 hours, then diluted with water (80 ml) and extracted with ethyl acetate (3 x 80 ml). The combined extracts were washed with saturated brine, dried (magnesium sulfate) and evaporated to a yellow oil. Trituration with diethyl ether gave the title compound as a yellow solid (390 mg). MS (ESP): 445 (MH*) for C20H21FN6O5
NMR (DMSO-d^ 5: 2.10 (s,3H); 2.42 (partly obscured by DMSO, 2H); 3.51-3.68 (m,2H); 3.94 (dd, 1H); 4.09 (m, 2H); 4.29 (t, 1H); 4.82 (m, 2H); 5.10-5.30 (m, 3H); 6.00 (m, 1H); 7.24 (m, 1H); 7.35-7.49 (m, 2H); 9.02 (s, 1H).
Example 73: (5K)-3-(4-(l-((2S\-2.1-Dihydroxvpropionyn-1.2.5.6-tetrahvdrnpvridin-4-yl)-3-fluorophenyI)-5-(tetrazoI~2-ylmethyI)oxazoIidin-2-one
(5i?)-3-(4-(l-((4S)-2,2-Dimetoyl-l^
fluorophenyl)-5-(tetrazol-2-ylmethyl)oxazolidin-2-one (550 mg, 1.17 mM) in a mixture of tetrahydrofuran (25 ml) and aqueous hydrochloric acid (1M, 10 ml) was stirred at room temperature for 24 hours, then concentrated by evaporation to a solid. The solid was filtered, washed with water, followed by a small volume of ethanoL, then triturated with diethyl ether to give the title compound as a colourless solid (450 mg). MS (ESP): 433(Mrr)forC19H21FN605
NMK rDMSO-d^ 8: 2.41 (partly obscured by DMSO, 2H); 3.41-4.42 (m, UK); 5.11-5.32 (m, 3H); 6.01 (m, 1H); 7.25 (m, 1H); 7.35-7.48 (m, 2H); 9.04 (s, 1H).
Eyample 74: r5JgV3-f4-tt-(2-HvriroYvar.etvn-1.2.5.6-tetrahydropvridin-4-yI)-3-fluoro-ph enylV 5-ftetrazol-2-yImeth vl WazoIidin-2-on e
'5#)-3-(4-(i-(2-Acetoxyacetyl)-l,2,5,6-tetrahydr^
^lmethyl)oxazolidin-2-one (365 mg, 0.82 mM) was treated with a saturated solution of

ammonia in methanol (40 ml), warmed slightly to dissolve completely, then stirred at room temperature for 20 hours. The solvent was evaporated to give an orange oil which was triturated with diethyl ether to give the title compound as a pale yellow solid (211 mg). MS (ESP): 403 (MET) for.ClgH19FNfi04
NMR (DMSO-dg) 5: 2.45 (partly obscured by DMSO, 2H); 3.50-3.70 (m, 2H); 3.92 (dd, IH); 4.03-4.19 (m, 4H); 4.30 (t, IH); 4.55-4.65 (m, IH); 5.10-5.31 (m, 3H); 5.95-6.04 (m, IH); 7.23 (m, IH); 7.34-7.48 (m, 2H); 9.04 (s, IH).
.1
Example 75: r5/?V3-f3.5-Diflaoro-4-(3.6-dihvdro-l.l-dioxo-2/y-thiopvran-4-ynpheny1V 5-ttetrazoI-l -ylmethvIWaznlidm-2-one and f5^-3-f3.5-Difluoro-4-f3.6-dihvdro-l .1 -dioxo-2.H'-thiopyran-4-yl)phenvr>-5-ftetrazol-2-yImethvnoxazolidin-2-one
(Ji?)-3-(3,5-Difluoro-4-(256-d^ydro-14-dUoxo-2^-tmopyran-4-yl)phenyl)-5-memane-
sulfonyloxymethyloxazolidin-2-one (437 mg, 1 mM), was treated with IH-tetrazole (105 mg,
1.5 mM) essentially as in Example 34 except that the mixture was heated to 75° for 2 hours.
Crude product after the ethyl acetate extraction was purified by chromatography on a 10 g
silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 100%
ethyl acetate in dichloromethane. Relevant fractions of the first eluting product were
combined to give the less polar tetrazol-2-yl isomer (206 mg).
MS (ESP): 412(MH+)forC16HJ5F2Ns04S
NMR (DMSO-d^) 5: 2.82 (m,2H); 3.32 (m overlapped by H20,~2H); 3.93 (overlapping
m, 3H); 4.28 (t, IB); 5.15 (d, IH); 5.24 (d, IH);. 5.30 (m, IH); 5.75 (br s, IH); 7.31 (d,
2H); 9.03 (s, IH).
The second eluting product was the 1-isomer (105 mg).
MSJCESE): 412 (MET) for Cl6El5F2^504S
NMR (DMSO-d_5) 5: 2.81 (m,2H); 3.33 (m overlapped by H20, ~2H); 3.92 (overlapping
m, 3H); 4.26 (t, IH); 4.93 (d, 2H); 5.18 (m, IH); 5.74 (s, IH); 7.31 (d, 2H); 9.48 (s, IH)-.
Example 76: (5J?V3-(4-n -TsnpropylsuIfonyl-1.2.5.6-tetrahydropyridin-4-vI)-3-fhioro-phenyIV5-(1.2.3-rria?:nl-t -ylmpithyDoxazolidm-2-one
(5i?)-3-(4-(l}2s5}6-Tetrahydropyridm-4-yl)-3-fluorophenyl)-5-(l5253-triazol-l-ylme%l)-oxazolidin-2-one hydrochloride (380 mg, 1 mM) was dissolved in water (5 ml), which was

then diluted with acetone (10 ml), and solid sodium bicarbonate (0.84 g, 10 mM) added. The mixture was stirred and cooled to 0°C, and isopropylsulfonyl chloride (285 mg, 2 mM) added dropwise. After stirring for 5 hours, an equal portion of sulfonyl chloride was added, and stirring continued for 18 hours. Most acetone was removed by evaporation, the residue diluted with water (50 ml), and extracted with ethyl acetate (3 x 20 ml). The extracts were washed with brine and dried (magnesium sulfate). The residual oil after evaporation was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (205 mg). MS (ESP): 450 (MET) for C^FN^S
NMRftDHj) 8: 1.37 (d, 6H); 2.53 (br, 2H); 3.22 (heptet, 1H); 3.56 (td, 2H); 3.94 (dd, 1H); 4.03 (m, 2H); 4.16 (t, 1H); 4.78 (d, 2H); 5.06 (m, 1H); 5.92 (m, 1H); 7.07 (dd, 1H); 7.19 (td, 1H); 7.29 (dd, 1H); 7.74 (d, 1H); 7.78 (d, IF).
Example 77: f5J?^3-r4-ri-Methvlsulfonyl-1.2.5.6-tetrahvdropyridin-4-ylV3-flnoro-phenvl)-5-(1.2.3-triazol-l-ylmethyl)oxazolidm-2-one
(5i2)-3-(4-(l,2,5,6-Terrahydropyridm-4-yl)0-fluorophenyl)-5-(l,2,3-triazol-l-ylme^ oxazolidin-2-one hydrochloride (380 mg,-1 mM) was suspended in dichloromethane (15 ml), 4-d^emylaminopyridine (305 mg, 2.5 mM) added, and the mixture stirred vigorously for 15 minutes. After cooling to 0°C under nitrogen, methanesulfonyl chloride (229 mg, 2 mM) was added dropwise, and the mixture stirred 18 hours at ambient temperature. Precipitated solid was removed, and the organic solution concentrated, then purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 5% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (30 mg). MSiESE): 422 (MIT) for C18H20FN5O4S
NMRfDMSO-d^ 5: 2.52 (br, 2H); 2.92 (s, 3H); 3.34 (t, 2H); 3.84 (m, 2H); 3.89 (dd, 1H); 4.23 (t, 1H); 4.82 (d, 2H); 6.01 (br, 1H); 7.23 (dd, 1H); 7.36 (t, 1H); 7.40 (dd, 1H); 7.74 (d, 1H); 8.14 (d, 1H).

Example 78: riigl-S-M-n-EtliylsulfonvI-l.Z.S.g-tetrahydropyridin^-yn-S-fluorophenyn-5-(1.2.3-triazol-l-yImethvr>oxazoIidin-2-one
(5i?)-3^4-(l,2,5,6-Tetrahydropyridm-4-yl)-3-fluorophenyl)-5 NMR (CDCy 5: 1.39 (t, 3H); 2,55 (br, 2H); 3.02 (q,2H); 3.53 (t,2H); 3.94(dd,lH); 3.99 (m, 2H); 4.16 (t, IH); 4.78 (d, 2H); 5.06 (m, IH); 5.92 (br, IH); 7.06 (dd, IH); 7.19 (t, IH); 7.29 (dd, IH); 7.74 (d, IH); 7.78 (d, IH).
Example 79: (5SW-(4-(1 -TrifliioromethyIsnlfonvI-1.2.5.6-tetrahvdropyridin-4-yn-3-flnorophenyn-5"fl.2.3-triazol-1-ylmethyl)oxazolidin"2"0ne
(5J?)-3-(4-(l,2,5,6-Tetrahydropyrio^"4-yl)-3"fluorophenyl)-5-(l,2,3-Mazol-l-ylmemyl)-oxazolidin-2-one hydrochloride (380 mg, 1 mM) was treated with trifluoromethanesulfonyl chloride essentially as in Example 76. Crude material was purified by chromatography on a 5 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 10% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (444 mg). MS (ESP): 476 (MIT) for C,8H17F4N504S NMR rDMSO-d,') 5: 2.55 (br, 2H); 3.71 (t, 2H); 3.88 (dd, IH); 4.16 (m, 2H); 4.23 (t, IH); 4.81 (d,2H); 5.13 (m, IH); 6.02(br,lH); 7.24 (dd, IH); 7.38 (t, IH); 7.42(dd,lH); 7.74 (d, IH); 8.14 (d, IH).
Example 80: f5JgV3-r4-ri-f3-Ch1oropropvnsulfonyl-1.2.5.6-tetrahvdrnpvridm-4-vD~3-fluorophenv1V5-n.2.3-triazol-l-vlmethvnnxazoIidin-2-one
(5i?)-3 NMR rDMSO-d.) 8: 2.12 (quintet, 2H); 2.49 (br, obscured by DMSO,~2H); 3.21 (t,2H); 3.42 (t,2H); 3.73 (t,2H); 3.89 (overlapping m,3H); 4.23 (t, IH); 4.82 (d,2H); 5.13 (m,

IE); 6.01 (br, 1H); 7.23 (dd, 1H); 7.35 (t, 1H); 7.41 (dd, IE); 7.74 (d, 1H); 8.14 (d51H).
Example 81: r5gV3-r4-fl-f2-MethoxyethvnsnlfonvI-1.2.5.6-tetrahvdropvridin-4-yn-^-fluorophenvn-5-n.2.3-triazoI-l-ylmethynoxazoIidm-2-oiie
(JJ?)-3-(4-(l,2,5,6-Tetraliydropy^
oxazolidin-2-one hydrochloride (380 mg, 1 mM) was treated with 2-methoxyethylsulfonyl
chloride essentially as in Example 79. Chromatography gave the desired product (65 mg).
MS fESP): 466 (MET) for C20H24FN505S
NMRCCDCI^ 8: 2.55 (br, 2H); 3.25 (t, 2H); 3.37 (s, 3H); 3.50 (t, 2H); 3.77 (t, 2H); 3.92
(m, 1H); 3.97 (m, 2H); 4.16 (t, IE); 4.78 (d, 2H); 5.06 (m, 1H); 5.91 (br, 1H); 7.06 (dd,
IB); 7.18 (t, 1H); 7.29 (dd, 1H); 7.74 (d, 1H); 7.78 (d, 1H).
Example 82 : f5i?V3-r3-FIuoro-4-(;/
(J^-S-^S^-dmydro^H-thiopyran^-yO-S-fluorophenyll-S^l^^-triazol-l-ylmethyl)oxazolidin-2-one (Example 83; 1.25 g, 3.5 mmol) was stirred in a mixture of methanol and ethyl acetate (1:1, 50 ml) at ambient temperature. Sodium periodate (0.93 g, 4.3 mmol) in water (10 ml) was added dropwise, and it was stirred for 18 hours. Precipitated salts were removed by filtration and solvents were removed under vacuum. The residue was chromatographed on silica gel, washing with 25% acetone in dichloromethane, then eluting with 5 to 7% methanol in dichloromethane to give the title product (1.152 g). MS (ES?): 377 (MIT) for C17HnKNAS Lff-NMR fDMSO-dfr) 8: 2.57 (m, 1H); 2.91 (m, 1H); 2.97 (m, 1H); 3.13 (m, 1H); 3.39 (m,
1H); 3.67 (m, 1H); 3.92 (dd, 1H); 4.27 (dd, 1H); 4.86 (m, 2H); 5.17 (m, 1H); 5.84 (m, 1H); 7.28 (dd, IK); 7.39 (dd, 1H); 7.45 (dd, 1H); 7.79 (d, 1H); 8.20 (d, 1H).

Example 83 : f5JgV3-f4-r3.6-dihydro-2g-thiopyran-4-v1V^-fliinrophenyl]-5-fl.2.3-triazoI-l-vlmethyl)oxazolidin-2-one

(5J?)-3-[4-(3,6-dmydro~2#-fluopy^^
(2g, 5.7 mmol) was dissolved in dioxane (10 ml). BicycIo[2.2.1]hepta-2,5-diene (3.1 ml, 28.7
mmol) was added and it was refluxed under nitrogen for 18 hours. The solvent was
evaporated in vacuo and the residue subjected to chromatography on silica gel eluting with
25% ethylacetate in dichloromethane to give the title compound (1.51 g).
MS (ESP): 361 (MIT) for C17H17FN402S
J-H-NMR fDMSO-d£> 5: 2.56 (m, 2H); 2.83 (dd, 2H); 3.31 (m, 2H); 3.91 (dd, IH); 4.26
(dd, IH); 4.86 (m, 2H); 5.17 (m, IH); 6.06(m, IH); 7.25 (dd, IH); 7.33 (dd, IH); 7.42 (dd, IH); 7.78 (d, IH); 8.19 (d, IH).
The above Examples 82 & 83 were prepared from the intermediates below:
(5i?V3-[4-(3.6-dihvdro-2i7-tMopwaTi^v1V3-fluorophenvl]-5-azidomethvloxa7olidin-2-one
Metbanesulfomc acid (5i?)-3-[4-(3,6-dih^^
oxazolidin-5-ylmethyl ester (8 g, 19.7 mmol) and sodium azide (4 g, 61.5 mmol) were heated
in N,N-dimethylformarnide (75 ml) at 80°C for 2 hours. It was cooled to room temperature,
diluted with ethyl acetate, washed with potassium phosphate buffer (pH 7) and with water and
dried over sodium sulfate. After evaporation of the solvent the title product was obtained as a
brown oil (~7 g, crude).
iH-NMR (DMSO-d^) 5: 2.56 (m, 2H); 2.83(dd,2H); 3.31 (m,2H); 3.71 (dd, IH); 3.80
(dd,lH); 3.81 (dd, IH); 4.17(dd,lH); 4.92 (m, IH); 6.06(m, IH); 7.34 (m,2H); 7.50 (m, IH).

Methanesulfomcacid(5J?)-3-[4-(3.6-dihydro-2i7-thiopyran-4-yl)-3-fluorop|ienyI]-2-oxo-oxazolidm-5-vlmethvl ester

(5i?)-3-[4-(3,6-dihydro-2F-tMopyran^-yl)-3-3Quorophenyl]-5-hydroxymethyloxazoUdin-2-one (14 g, 45.3 mmol) was dissolved in dichloromethane (300 ml) and triethylamine (8.8 ml, 63.3 mmol) was added. It was cooled to -20°C and methanesulfonyl chloride (4.22 ml, 54.4 mmol), dissolved in dichloromethane (50 ml), was added dropwise. The reaction mixture was allowed to warm to room temperature and was quenched with potassium phosphate buffer (pH 7). Dichloromethane was removed under vacuum and it was extracted with ethyl acetate, washed with water and dried over magnesium sulfate. The title compound (16.9 g) was precipitated from dichloromethane by addition of hexane. ^-NTVTR rPMSO-d^ 5: 2.56 (m, 2H); 2.83 (dd, 2H); 3.28 (s, 3H); 3.32 (m, 2H); 3.85 (dd,
1H); 4.21 (dd, 1H); 4.48 (dd, 1H); 4.53 (dd, 1H); 5.04 (m, 1H); 6.07 (m, 1H); 7.33 (dd, 1H); 7.36 (dd, 1H); 7.50 (dd, 1H).
(5i?)-344-(3-6-dihvdro-2F-thiopyran-4-yl)-3-fluorophenv1]-5-hvdroxvmethvloxa7o1idm-2-
sns
4-(2-Fluoro^benzyloxycarbonylammophenyl)-3,6-dmydro-2i^tbiopyran (15.3 g, 44.6 mM) was dissolved in dry tetrahydrofuran (175ml) and stirred under nitrogen at -70°C. n-ButylUthium (1.6M in hexanes, 30ml, 175 mM) was run in over 20 minutes, keeping the temperature below -60°, and the mixture then stirred a further 10 minutes at -70°C. A solution of (iJ)-glycidyl butyrate (6.42 g, 44.62 mM) dissolved in dry tetrahydrofuran (10 ml) was added dropwise over 10 minutes keeping temperature below -60°, and the mixture left to warm to ambient temperature over 18 hours. Methanol (29ml) was added, and the mixture stirred for 10 minutes only. Saturated aqueous sodium bicarbonate (200 ml) was added, and the mixture extracted with ethyl acetate (400 ml). The extract was washed with saturated aqueous sodium bicarbonate (100ml), brine (100ml), dried (magnesium sulfate). Filtered and

evaporated. The crude product was purified on a 300 g silica sinter column, eluting with a gradient from 0% to 100% ethyl acetate in dichloromethane. Relevant fractions were combined, reduced to a small volume, and diluted with an excess of is^hexane to precipitate the desired product (11.3 g). MS (ESP): 310 (MIT) for C15H16FN03S NMR rDMSO-d^ 6: 2.52 (m overlapped by DMSO,~2H); 2.78 (t,2H); 3.27 (m, 2H);
3.52 (m, IB); 3.65 (m, 1H); 3.80 (dd, 1H); 4.06 (dd, 1H); 4.65 (m, 1H); 5.19 (t, 1H); 6.01 (s, 1H); 7.28 (m, 2H); 7.47 (dd, 1H).
4-(2-Fluoro-4-benzyloxvcarhonvlaminophenvD-3.6-dihvdro-2g-thiopvran

4-(2-Fluoro-4-arm^ophenyl)-3,6-dihydro-2fl-thiopyran (9.8 g, 46.8 rnM) was dissolved in dry dichloromethane (196ml), pyridine (6.23g, 79.1 mM) added, and the mixture stirred under nitrogen at -20°. A solution of benzyl chloroformate (9.54g, 53.9 mM) dissolved in dry dichloromethane (25 ml) was added dropwise, and the mixture left to warm to ambient temperature over 18 hours. The mixture was washed with 1M hydrochloric acid (200 ml), then brine (100 ml), dried (magnesium sulfate), filtered and evaporated to a small volume. The addition of wohexane (300 ml) precipitated the desired product (15.5 g). MS (Negative ESP): 342 (M-H) for C19HI8FN02S NMR (DMSO-dgl 5: 2.50 (s,2H); 2.79 (t,2H); 3.26 (m,2H); 5.15 (s,2H); 5.99 (s, 1H);
7.18 (m, 2H); 7.38 (m, 6H); 10.01 (s, 1H).
4-(2-Fluoro-4-aminophenyl)-3.6-dihydro-2/f-thiopyran
4-Hya^oxy-4-(2-fluoro-4-aminophenyl)tetrahydrothiopyran (11.35 g, 50 mM) and butylated hydroxytoluene (50 mg) as antioxidant were suspended in a mixture of concentrated hydrochloric acid (37%, 200 ml) and water (50 ml), and stirred at 80° under nitrogen for 18 hours. Glacial acetic acid (150 ml) was added, and reaction continued at 80° for a further 5 hours. After cooling, the reaction was made basic by the cautious addition of concentrated ammonia and ice. The mixture was extracted with diethyl ether (400 ml), the extract washed with water (100 ml), brine (100 ml), dried (magnesium sulfate), filtered and evaporated to

give the title product (10 g) as a dark oil.
NMR (CPCIj) S: 2.59 (m,2H); 2.72 (t,2H); 3.30 (m,2H); 3.80 (far, 2H); 5.93 (m, IH);
6.35 (dd, IH); 6.39 (dd, IH); 6.97 (t, IH).
Example 84 : (5JgV3-f4-a.l-dioxo-3.6-dihydro-2H-thiopvrap-4-vn-^-fliinrophenvI|-5-fl.2.3-triazo1-l-vlmetfaynoxazoIidiii-2-oiie

(5^)-3-[4 2H); 5.18 (m, IH); 5.83 (m, IH); 7.29 (dd, IH); 7.40 (dd, IH); 7.47 (dd, IH); 7.78 (s, IH); 8.19 (s, IH).

Example 85: r5i?V3-r^.f;-T)ifliinrn-4-(7fg.ty)-OYo-3.6-dihvdro-2H-thiopvran-4-yIV phenyI]-5-ri.2.3-triazol-l-vImt>thvDoxazoIidin-2-one

(5i?)-3-[4-(3,6-dihydro-2^thiopyran-4-yl)-3,5-chfluorophenyl]-5-(l,233-triazol-l-ylmethyl)oxazolidin-2-one (Example 86; 0.86 g, 2.3 mmol) was stirred in a mixture of methanol and ethyl acetate (1:1,20 ml) at ambient temperature. Sodium periodate (0.50 g, 2.4 mmol) in water (10 ml) was added dropwise, and the mixture stirred for 3 hours. Precipitated salts were removed by filtration and washed with ethyl acetate. The filtrate was washed with brine, dried over magnesium sulfate and concentrated to dryness. The residue was chromatographed on silica gel eluting with 5% methanol in dichloromethane to give the title product (0.69 g). MS fESP): 395 (MHT) for C17HJ6F2N403S ^H-NMR fDMSO-d^ 5: 2.41 (brs, 1H); 2.80 (m, 1H); 2.97 (brs, 1H); 3.15 (m, 1H); 3.39
(m,lH); 3.67 (brs, 1H); 3.94 (m, 1H); 4.25 (dd, 1H); 4.85 (brs, 2H); 5.19 (m, 1H); 5.75 (brs, 1H); 7.33 (d, 2H); 7.79 (brs, 1H); 8.20 (brs, 1H).
Example 86: r5i?)-3-f4-r3. Meftaaesulfomc acid (5i?)-3-[4-(3,6-dihy^
oxazohdin-5-ylmethyl ester (1.1 g, 5.7 mmol) was dissolved in dry N,N-dimethylformamide (5 ml) and sodium azide (0.35 g, 5.43 mmol) was added. It was heated at 60°C for 18 hours. The reaction mixture was cooled to room temperature, diluted with ethylacetate, washed with water and dried over magnesium sulfate. Solvent was removed under vacuum to give an oil. The crude intermediate azide was not characterized. It was taken up in 1,4-dioxane (20 ml), bicyclo[2.2.1]hepta-2,5-diene (1.0 g, 10.9 mmol) was added and it was refluxed for 12 hours. Solvent was removed under vacuum and the residue chromatographed on silica gel with 5% methanol in dichloromethane to give the title compound (0.62g).

MS (ESP): 379 (MrT) for C17H1SF2N402S
NMR (DMSO-d^) 8: 2.43 (brs, 2H); 2.83(dd,2H); 3.31. (brs, 2H); 3.92 (m, IH); 4.25 (dd,
IH); 4.84 (d,2H); 5.18 (m, IH); 5.98 (brs, IH); 7.28 (d,2H); 7.79 (brs, IH); 8.19 (brs, IH).
The above Examples 85 & 86 were prepared from the intermediates prepared analagously to those used in Examples 82 & 83.
Example 87 :f5J?V3-f3r5-Diflnoro-4.fJr3?.,y)-oxo-3.6-dihvdro-2H-thiopvran-.4-yn-pheiivIl-5-(1.2.3-triazoI-2-yImethyI)oxazoIidin-2-one

(5iJ)-3-[4 folH); 3.67 (brs, IH); 3.93 (m,lH); 4.26 (dd, IH); 4.88 (m,2H); 5.24(m, IH); 5.76 ^rd, IH); 7.31 (d,2H); 7.86 (s,2H).

Example 88 : r5J?V3-[4-r3.6-dihydrn-2fl-thiopvran-4-vn-3.5-difluornphenvl|^-n.'Z.^-triazol-2-yImetbyfloxazolidin~2-one

Sodium hydride (60% in oil, 148 mg, 3.7 mmol) was suspended in dry N,N-dimethylformamide (5 ml) and 1,2,3-triazole (0.26 g, 3.7 mmol) was added under nitrogen. It was stirred for 5 minutes at room temperature and methanesulfonic acid (5i?)-3-[4-(3,6-dmydro-2/y-tm^pyran-4-yl)-3,5-difluorophenylJ-2-oxo-oxazoHdm-5-ylmethyl ester (see Example 86; 1.0 g, 2.47 mmol) was added. It was heated to 75°C for 3.5 hours, then cooled to room temperature, diluted with aqueous sodium hydrogencarbonate solution (5%, 100 ml) and extracted with ethylacetate (2 x 100 ml). The organic phase was washed with water (2 x 50 ml), brine (100 ml), dried over magnesium sulfate and the solvent was evaporated in vacuo. Chromatography on silica gel with a gradient of 10-50% ethylacetate in hexanes gave the title compound (0.65g). MS (ESP^: 379. (Mff) for C17H16F2N402S
NMR (CDCL) 6: 2.53 (m, 2H); 2.89 (dd, 2H); 3.35 (m, 2H); 3.95 (m, 1H); 4.25 (dd, 1H); 4.83 (m, 2H); 5.09 (m, 1H); 5.96 (brs, 1H); 7.05 (d, 2H); 7.79 (d, 2H).
Example 89: 5rRVf3-Oxo-isoxazo]-2^vlmethvlV3-r4-fl.2.f).6-tetrahvdropvrid-4-vn-3.5-difluorophenyI)oxazoIidin-2-one
PCT Application No. GB99/01753 (Publication No. WO 99/64417) describes the preparation of 5(R)-Hydroxyme%l-3
During the Mitsunobu reaction the ambident nucleophile 3-hydroxyisoxazole reacts with
S(R)-Hydroxymethyl-S^^Cl-benzyl^^^^-terrahydropyrid-^-yl)^^-
difluorophenyl)oxazolidin-2-one to give a quantity of S^HS-Oxo-isoxazol^-ylmethylJ-S-^-
fl-bei^M^S^etrahydropyrid^-yty-S^-difluoro^ Failure to
purify (e.g. by suitable column chromatography) the product from the Mitsunobu reaction
described in GB99/01753 before subsequent reaction with 1-chloroethyl chloroformate and
work-up using hydrochloric acid gives a quantity of 5(R)-(3-Oxo-isoxazol-2-yhnethyl)-3-(4-
(l^jSje-tetrahydropyrid^-ylJ-SjS-difluoropheny^oxazoHdin^-one as the hydrochloride salt,
which is identified in the mixture by correlation TOCSY NMR (TOtal Correlation
Spectroscopy) - methylene carbon attached to the nitrogen of the isoxazolone ring has a shift *
of 48 ppm (characteristic of this linkage), and by LC-MS (MH+ 378 - less chloride) using C-
18 Hichrom RPB column, 5mm, 25cm x 0.46mm i.d; Eluant - 650ml Water, 350ml
Acetonitrile, 1ml TFA (biograde); Flow - 1.5ml/min; Retention Times N-linked Piperidene -
Rt = 2.0 min, O-linked Piperidene - Rt = 3.25 min.

( -one
To 3-tert-butoxy-2(S)-hydroxypropanoic acid (343 mmol) in dimethylformarnide (DMF) at iO-25°C was added (4-(l,2,5,6-tetrahydropyrid-4-yl)-3,5-difiuorophenyl)oxazoHdin-2-one lydrochloride salt (264 mmol; Reference Example 6 of GB99/01753, prepared as described in

Example 89 without purification following the Mitsunobu reaction of 3-hydroxyisoxazole reacts with 5(R)-Hydroxymethyl-3-(4-(l-benzyl-1,2}5,6-tetrahydropyrid-4-yl)-3,5-&fluorophenyl)oxazolidin-2-one). To the mixture was added 1-hydroxybenzotriazole hydrate (HOBt; 0.4 eq.) and further DMF (to 6 vol.). The solution was placed under a nitrogen atmosphere, cooled to 16-18°C and Et3N (1.5 eq.) added. l-[3-(Dimethylamino)propyl]-3-ethylcarbodiirnide hydrochloride (EDO; 1.4 eq.) dissolved in water (1.5 vol.) was added dropwise keeping the temperature below 25°C. After approximately one hour the reaction :was complete and tert-butyl methylether (MTBE; 1 vol.) followed by water (12 vol.) was added. After vigorous stirring for 1 hour the resultant solid was filtered, washed with water and MTBE, and dried under vacuum at 35-40°C.
The resultant product (3.71 kg) was dissolved in DCM (8.5 litres) and purified by column chromatography eluting with EtOAc/iso-hexane (80:20) collecting the appropriate fractions and removing the solvent under reduced pressure to give 5(R)-Isoxazol-3-yloxymethyl-3-(4-(l-(34ert-butoxy-2(S)-hydYoxypropanoyl)-l,2,5,6-tetrahydropyrid-4-yl)-3,5-difluorophenyl)oxazoUdin-2-one as a white foam (3.03 kg, 82% yield). The column was eluted further with methanol (50.5 litres) and the solvent removed under reduced pressure to give a brown gum (100 g). Trituration of the gum with EtOAc (500 ml) gave the title compound as a dark yellow solid (1 OOg).
IR (KBr disk) (ran1) 1737 (CO, oxazolidinone), 1638 (CO, amide); MS (MH+) 522; JHNMR(500MHz) assigned via TOCSY and HMQC (Heteronuclear Multiple Quantum Coherence spectra - A 1H/13C correlation) - methylene carbon attached to the nitrogen of the isoxazolone ring has a shift of 49 ppm (characteristic of this linkage).

Example 90 (5.0g) was slurried in 4M HC1 in dioxane (25ml) and stirred at ambient temperature for 24 hours. The gum that formed was washed with dioxane (20 ml) and

triturated with isobutanol (50 ml). The solid that resulted was washed with isobutanol (2x10 ml) and dried under reduced pressure to give the title, compound as a yellow solid (3.4g). XH NMR (500MHz) assigned via TOCSY and HMQC correlation spectra. Methylene carbon attached to the nitrogen of the isoxazolone ring has a shift of 47 ppm (characteristic of this linkage vs O-linkage); MS (MH+) 466.
Example 92
The following illustrate representative pharmaceutical dosage forms containing a compound of the formula (I), an in-vivo hydrolysable ester or a pharmaceutically-acceptable salt thereof, including a pharmaceutically-acceptable salt of an in-vivo hydrolysable ester, (hereafter compound X), for therapeutic or prophylactic use in humans:
(a) Tablet I mg/tablet
CompoundX 500
Lactose Ph.Eur 430
Croscarmellose sodium 40
Polyvinylpyrrolidone 20
Magnesium stearate 10
(b) Tablet n mg/tablet
Compound X 100
Lactose Ph.Eur 179
Croscarmellose sodium 12
Polyvinylpyrrolidone 6
Magnesium stearate 3
(c) Tablet HI mg/tablet
CompoundX 50
Lactose PLEur. 229
Croscarmellose sodium 12
Polyvinylpyrrolidone 6
Magnesium stearate 3
(d) Tablet IV mg/tablet
CompoundX 1

Lactose Ph.Eur 92
Croscarmellose sodium 4
Polyvinylpyrrolidone 2
Magnesium stearate 1
Capsule mg/capsule
Compound X 10
Lactose Ph.Eur 389
Croscarmellose sodium 100
Magnesium stearate 1
Injection I
Compound X 50% w/v
Isotonic aqueous solution to 100%
Injection H (e.g. bolus)
Compound X 10% w/v
Isotonic aqueous solution to 100%
Injection TIT
CompoundX 5% w/v
Isotonic aqueous solution to 100%
Injection IV (e.g. infusion)
Compound X 1% w/v
Isotonic aqueous solution to 100%
Buffers, pharmaceutically-acceptable surfactants, oils or cosolvents such as polyethylene glycol, polypropylene glycol, glycerol or ethanol, glidants (such as silicon dioxide) or complexing agents such as a cyclodextrin (for example, hydroxypropyl B-cyclodexrrin or sulfobutylether fl-cyclodextrin) may be used to aid formulation. Also, improvements in aqueous solubility, if desired, maybe achieved, for example, by conjugation of a compound of formula (1) with a phospholipid (such as a (phospho)choline derivative) to form a micellar emulsion.
Note: The above formulations may be obtained by conventional procedures well known in the pharmaceutical art, for example as described in "Remington: The Science & Practice of

Pharmacy" Vols. I & II (Ed. A.R.Gennaro (Chairman) et al; Publisher: Mack Pubhshing Company, Easton, Pennsylvania; 19th Edition -1995) and 'Tharmaceutics - The Science of Dosage Form Design" (Ed. M.E.Aulton; Publisher: Churchill Livingstone; first published 1988). The tablets (a)-(d) may be (polymer) coated by conventional means, for example to provide an enteric coating of cellulose acetate phthalate.

1. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-
hydrolysable ester thereof, '

wherein
HET is an N-linked 5-membered heteroaryl ring, containing either (i) 1 to 3 further nitrogen
heteroatoms or (ii) a further heteroatom selected from 0 and S together with an optional
further nitrogen heteroatom; which ring is optionally substituted onaC atom by an oxo or
thioxo group; and/or the ring is optionally substituted on a C atom by 1 or 2 (l-4C)alkyl
groups; and/or on an available nitrogen atom (provided that the ring is not thereby
quaternised) by (l-4C)a!kyl; or
HET is an N-linked 6-membered heteroaryl ring containing up to three nitrogen heteroatoms
in total (including the linking heteroatom), which ring is substituted on a suitable C atom by
oxo or thioxo and optionally substituted on any available C atom by 1 or 2 (l-4C)alkyl
substituents;
Q is selected from Ql to Q9 :-

wherein R2 and R3 are independently hydrogen or fluoro;
wherein A3 is carbon or nitrogen; Bj is O or S (or, in Q9 only, NH); Xq is O, S or N-R1
(wherein R1 is hydrogen, (l-4C)alkyl or hydroxy~(l-4C)alkyl); and wherein
in Q7 each Aj is independently selected from carbon or nitrogen, with a maximum of 2
nitrogen heteroatoms in the 6-membered ring, and Q7 is linked to T via any of the At atoms
(when A, is carbon), and linked in the 5-membered ring via the specified carbon atom, or via
Ax when At is carbon; Q8 is linked to T via either of the specified carbon atoms in the 5-
membered ring, and linked in the benzo-ring via either of the two specified carbon atoms on
either side of the linking bond shown; and Q9 is linked via either of the two specified carbon
atoms on either side of the linking bond shown;
wherein T is selected from the groups in (TA) to (TD) below (wherein AR1, AR2, AR2a,
AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1 and CY2 are defined hereinbelow);
(TA) T is selected from the following groups :-
(TAa) AR1, ARl-(l-4C)alkyl-, AR2 (carbon linked), AR3;
(TAb) ARl-CH(OH), AR2-CH(OH)-, AR3-CH(OH)-;
(TAc) ARl-CO-,AR2-CO-9AR3-CO-,AR4-CO-;
(TAd) AR1-0-, AR2-0-, AR3-0-;
(TAe) AR1-S(0)q-, AR2-S(0)q-, AR3-S(0)q- (qis 0,1 or 2);

(TAf) an optionally substituted N-linked (fully unsaturated) 5-membered heteroaryl ring system containing 1,2 or 3 nitrogen atoms;
(TAg) a carbon linked tropol-3-one or tropol-4-one, optionally substituted in a position not adjacent to the linking position; or
(TB) T is selected from the following groups :-
(TBa) haloor(l-4C)alkyl
{optionally substituted by one or more groups each independently selected from hydroxy, (1-
4C)alkoxy, (l-4C)alkanoyl, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, -NRvRw, (1-
6C)alkanoylamino, (l-4C)alkoxycarbonylamino, H-(l-4C)alkyl-M-(l-6C)alkanoylarnino, (1-
4C)alkylS(0)q- (q is 0,1 or 2), CY1, CY2 or AR1};
(TBb) -NRv'Rw1;
(TBc) ethenyL 2-(l-4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-((l-4Qaltylarnmocarbonyl)ethenyl, 2-((l-4C)alkoxycarbonyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl;
(TBd) R10CO-, R10S(O)q- (q is 0,1 or 2) or RI0CS-
wherein R10 is selected from the following groups :-
(TBda) CYlorCY2;
(TBdb) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw, ethenyl, 2-(l-
4C)alkylethenyl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyI, 2-nitro-2-
((l-4C)alkyl)ethenyl, 2-((l-4C)alkylarninocarbonyl)ethenyli 2-((l-
4C)alkoxycarbonyl)ethenyl, 2-(ARl)ethenyl or 2-(AR2)ethenyl; or
(TBdc) (l-4C)alkyl {optionally substituted as defined in (TBa) above, or by (1-
4C)alkylS(0)pNH- or (l-4C)alkylS(0)p.((l-4C)alkyl)N- (p is 1 or 2)};
wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl; Rv1 is hydrogen, (1-
4C)alkyl or (3-8C)cycloalkyl; Rw1 is hydrogen, (l-4C)alkyl, (3-8C)cycloallcyl, (l-4C)alkyl-
CO- or (l-4C)alkylS(0)q- (q is 1 or 2); or
(TQ T is selected from the following groups :-
(TCa) an optionally substituted, fully saturated 4-membered monocyclic ring containing 1
heteroatom selected from 0, N and S (optionally oxidised), and linked via a ring nitrogen or

sp3 carbon atom;
(TCb) an optionally substituted 5-menibered monocyclic ring containing 1 heteroatom
selected from 0, N and S (optionally oxidised), and linked via a ring nitrogen atom or a ring
sp3 or sp2 carbon atom, which monocyclic ring is folly saturated other than (where
appropriate) at a linking sp2 carbon atom;
(TCc) an optionally substituted 6- or 7-membered monocyclic ring containing 1 or 2
heteroatoms independently selected from O, N and S (optionally oxidised), and linked via a
ring nitrogen atom or a ring sp3 or sp2 carbon atom, which monocyclic ring is fully saturated
other than (where appropriate) at a linking sp2 carbon atom; or
(TD) T is selected from the following groups :-
(TDa) a bicyciic spiro-ring system containing 0,1 or 2 ring nitrogen atoms as the only ring
heteroatoms, the structure consisting of a 5- or 6-membered ring system (linked via a ring
nitrogen atom or a ring sp3 or sp2 carbon atom) substituted (but not adjacent to the miking
position) by a 3-, 4- or 5-membered spko-carbon-linked ring; which bicyciic ring system is
(i) fully saturated other than (where appropriate) at a linking sp2 carbon atom;
(ii) contains one -N(Rc)- group in the ring system (at least two carbon atoms away from
the linking position when the link is via a nitrogen atom or an sp2 carbon atom) or one -N(Rc)-
group in an optional substituent (not adjacent to the linking position) and is
(hi) optionally further substituted on an available ring carbon atom; or
(TDb) a 7-, 8- or 9-membered bicyciic ring system (linked via a ring nitrogen atom or a ring
sp3 or sp2 carbon atom) containing 0,1 or 2 ring nitrogen atoms (and optionally a further O or
S ring heteroatom), the structure containing a bridge of 1,2 or 3 carbon atoms; which bicyciic
ring system is
(i) fully saturated other than (where appropriate) at a linking sp2 carbon atom;
(ii) contains one 0 or S heteroatom, or one -N(Rc)- group in the ring (at least two carbon
atoms away from the linking position when the link is via a nitrogen atom or an sp2 carbon
atom) or one -N(Rc)- group in an optional substituent (not adjacent to the linking position)
and is
(in) optionally further substituted on an available ring carbon atom;

wherein Re is selected from groups (Rcl) to (Rc5) :-
(Rcl) (l-6C)alkyl {optionally substituted by one or more (l-4C)alkanoyl groups (including geminal disubstitution) and/or optionally monosubstituted by cyano, (l-4C)alkoxy, trifluoromethyl, (l-4C)alkoxycarbonyl, phenyl (optionally substituted as for AR defined hereinafter), (l-4C)alkylS(0)q- (q is 0,1 or 2); or, on any but the first carbon atom of the (1-6C)alJkyl chain, optionally substituted by one or more groups (including geminal disubstitution) each independently selected from hydroxy and fluoro, and/or optionally monosubstituted by oxo, -NRvRw [wherein Rv is hydrogen or (l-4C)a!kyl; Rw is hydrogen or (l-4C)alkyl], (l-6C)alkanoylamino, (l-4C)alkoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylamino, (l-4C)alkylS(0)pNH- or (l-4C)alkylS(0)p.((l-4C)alkyl)N- (p is 1 or 2)};
(Rc2) R13CO-,R13S02-orR13CS-
wherein R13 is selected from (Rc2a) to (Rc2e) :-
(Rc2a) AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b, AR4, AR4a, CY1, CY2;
(Rc2b) hydrogen, (l-4C)alkoxycarbonyl, trifluoromethyl, -NRvRw [wherein Rv is
hydrogen or (l-4C)alkyl; Rw is hydrogen or (l-4C)alkyl], ethenyl, 2-(l-4C)alkylethenyl, 2-
cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl, 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl,
2-((l-4C)alkylaminocarbonyl)ethenyl,
2-((l-4C)alkoxycarbonyl)ethenyl3 2-(ARl)ethenyl, 2-(AR2)ethenyl, 2-(AR2a)ethenyl;
(Rc2c) (l-10C)alkyl
{optionally substituted by one or more groups (including geminal disubstitution) each
independently selected from hydroxy, (1-10C)alkoxy, (l-4C)alkoxy-(l-4C)alkoxy, (1-
4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxy, (l-4C)alkanoyl, phosphoryl [-0-P(0)(OH)2, and
mono- and di-(l-4C)alkoxy derivatives thereof], phosphiryl [-0-P(OH)2 and mono- and di-(l-
4C)alkoxy derivatives thereof], and amino; and/or optionally substituted by one group
selected from phosphonate [phosphono, -P(0)(OH)2, and mono- and di-(l-4C)alkoxy
derivatives thereof], phosphinate [-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives
thereof], cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-
4C)alkoxycarbonyi, (l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxycarbonyL (l-4C)alkylamino,
di((l-4C)alkyl)amino, (l-6C)alkanoylamino, (l-4C)a]koxycarbonylamino, N-(l-4C)alkyl-N-
(l-6C)alkanoylamino, (l-4QalkylaminocarbonylJ di((l-4C)alkyl)aminocarbonyl, (1-
4C)altylS(0)prra-,(l-4C)altylS(0)p-((l-4C)^^

fluoro(l-4C)alkylS(0)p((14C)alkyl)N-, (l-4C)alkylS(0)q- [the (l-4C)alkyl group of (1-4C)aJkylS(0)q- being optionally substituted by one substituent selected from hydroxy, (1 -4C)alkoxy, (1 -4C)alkanoyl, phosphoryl [-O-P(0)(OH)2, and mono- and di-(l -4C)alkoxy ■ derivatives thereof], phospbiryl [-0-P(OH)2 and mono- and di-(l-4C)alkoxy derivatives thereof], amino, cyano, halo, trifluoromethyl, (l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxycarbonyl, (l-4C)alkoxy-(l-4C)alkoxy-(l-4C)alkoxycarbonyl, carboxy, (1-4C)alkylamino, di((l-4C)alkyl)arnino, (l-6C)alkanoylamino, (l-4C)aUcoxycarbonylamino, N-(l-4C)alkyl-N-(l-6C)alkanoylairnno, (l-4C)alkylaminocarbonyl, di((l-4C)alkyl)aminocarbonyl, (l-4C)alkylS(0)pNH-, (l-4C)aU (Rc2d) R14C(0)O(l-6C)aftyI wherein R14is AR1, AR2, (l-4C)aUcylamino (the (1-
4Qalkyl group being optionally substituted by (l-4C)alkoxycarbonyl or by carboxy), benzyloxy-(l-4C)alkyl or (l-10C)alkyl {optionally substituted as defined for (Rc2c)}; (Rc2e) R150- wherein R,s is benzyl, (l-6C)allcyl {optionally substituted as defined for (Rc2c)}, CY1, CY2 or AR2b;
(Rc3) hydrogen, cyano, 2-cyanoethenyl, 2-cyano-2-((l-4C)allcyi)ethenyl, 2-((l-4C)alkylaminocarbonyl)ethenyl, 2-((l-4C)alkoxycarbonyl)ethenyl, 2-nitroethenyl, 2-nitro-2-((l-4C)alkyl)ethenyl, 2-(ARl)ethenyl, 2-(AR2)ethenyl, or of me formula (Rc3a)

wherein X00 is -OR17, -SR17, -NHR17and -N(R17)2;
wherein R17 is hydrogen (when X00 is -NHRI7and -NfR17)^, and R17 is (l-4C)alkyl, phenyl or AR2 (when X00 is -OR17, -SR17 and -NHR17); and R16 is cyano, nitro, (l-4C)alkylsulfonyl, (4-7C)cycloalkylsulfonyl, phenylsulfonyl, (l-4C)ali:anoyl and (l-4C)alkoxycarbonyl;

(Rc4) trityl, AR1, AR2, AR2a, AR2b, AR3, AR3a, AR3b;
(RcS) RdOC(Re)=CH(C=0)-, RfC(=0)C(=0)-, RgN=C(Rh)C(=0)-or
RiNHC(Rj)=CHC(=0)- wherein Rd is (l-6C)alkyl; Re is hydrogen or (l-6C)alkyl, or Rd and
Re together form a (3-4C)alkylene chain; Rf is hydrogen, (l-6C)alkyL hydroxy(l-6C)alkyl,
(l-6C)alkoxy(l-6C)alkyl, -NRvRw [wherein Rv is hydrogen or (l-4C)alkyl; Rw is hydrogen
or (l-4C)alkyl], (l-6C)a!koxy, (l-6C)alkoxy(l-6C)alkoxy, hydroxy(2-6C)alkoxy, (1-
4C)alkylamino(2-6C)alkoxy, di-(l-4C)alkylamino(2-6C)alkoxy; Rg is (l-6C)alkyl, hydroxy
or (l-6C)alkoxy; Rh is hydrogen or (l-6C)alkyl; Ri is hydrogen, (l~6C)alkyl, AR1, AR2,
AR2a, AR2b and Rj is hydrogen or (1 -6C)alkyl;
wherein
AR1 is an optionally substituted phenyl or optionally substituted naphtbyl;
AR2 is an optionally substituted 5- or 6-membered, fully unsaturated (i.e with the maximum
degree of unsaturation) monocyclic heteroaryl ring containing up to four heteroatoms
independently selected from O, N and S (but not containing any O-O, O-S or S-S bonds), and
linked via a ring carbon atom, or a ring nitrogen atom if the ring is not thereby quaternised;
AR2a is a partially hydrogenated version of AR2 (i.e. AR2 systems retaining some, but not
the full, degree of unsaturation), linked via a ring carbon atom or linked via a ring nitrogen
atom if the ring is not thereby quaternised;
AR2b is a fully hydrogenated version of AR2 (i.e. AR2 systems having no unsaturation),
linked via a ring carbon atom or linked via a ring nitrogen atom;
AR3 is an optionally substituted 8-, 9- or 10-membered, fully unsaturated (i.e with the
maximum degree of unsaturation) bicyclic heteroaryl ring containing up to four heteroatoms
independently selected from 0, N and S (but not containing any 0-0, O-S or S-S bonds), and
linked via a ring carbon atom in either of the rings comprising the bicyclic system;
AR3a is a partially hydrogenated version of AR3 (i.e. AR3 systems retaining some, but not
the full, degree of unsaturation), linked via a ring carbon atom, or linked via a ring nitrogen
atom if the ring is not thereby quaternised, in either of the rings comprising the bicyclic
system;
AR3b is a fully hydrogenated version of AR3 (i.e. AR3 systems having no unsaturation),
linked via a ring carbon atom, or linked via a ring nitrogen atom, in either of the rings
comprising the bicyclic system;

AR4 is an optionally substituted 13- or 14-membered, fully unsaturated (i.e with the maximum degree of unsaturation) tricyclic heteroaryl ring containing up to four heteroatoms independently selected from O, N and S (but not containing any O-O, 0-S or S-S bonds), and linked via a ring carbon atom in any of the rings comprising the tricyclic system; CY2 is an optionally substituted cyclopentenyl or cyclohexenyl ring.
■
2. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, ^ claimed in claim 1; wherein Q is Ql wherein R2 md R3 arQ independently hydrogen or fluoro; ^6. the groups defined in (TCa) to (TCc) are defined by formulae (TCI) to (TC4) :-

wherein in (TCI) : >A3-B3- is >C(Rq)~CH(Rr)- and G is -0-, -S-, -SO-, -S02- or >N(Rc); wherein in (TC2) : ml is 0,1 or 2; >A3-B3- is >C=C(Rr)- or >C(Rq)-CH(Rr)- and G is -0-, -
!-,-SO-,-S02-or>N(Rc);
therein in (TC3): ml is 0,1 or 2; >A3-B3- is >C(Rq)-CH(Rr)- (other than when Rq and Rr
re both together hydrogen) and G is -0-, -S-, -SO-, -S02- or >N(Rc);
/herein in (TC4) : nl is 1 or 2; ol is 1 or 2 and nl + ol = 2 or 3; >A3-B3- is >C=C(Rr)- or
-C(Rq)-CH(Rr)- or >N-CH2- and G is -0-, -S-; -SO-, -S02- or >N(Rc); Rp is hydrogen, (1-4C)alkyl (other than when such substitution is defined by >A3-B3-), hydroxy, (l-4C)allcoxy or (l-4C)alkanoyloxy; wherein in (TCI), (TC2) and (TC4); ml, nl and ol are as defined hereinbefore:

>A3-B3- is >N-CH2- and G is >C(RU)(R12), >C=0, >C-OH, >C-(l-4C)alkoxy, >C=N-OH,
>C=N-(l-4C)alkoxy, X>N-NH-(l-4C)alkyl, >C=N-N((l-4C)alkyl)2 (the last two (1-
4C)alkyl groups above in G being optionally substituted by hydroxy) or >C=N-N-CO-(l-
4C)alkoxy; wherein > represents two single bonds;
Rq is hydrogen, hydroxy, halo, (l -4C)alkyl or (1 -4C)alkanoyloxy;
Rr is (independently where appropriate) hydrogen or (l-4C)alkyl;
Ru is hydrogen, (l-4C)alkyl, fluoro(l-4C)alkyl, (l-4C)alkyl-thio-(l-4C)alkyl orhydroxy-(l-
4C)alkyl and R12 is -[C(Rr)(Rr)]^-N(Rr)(Rc) wherein m2 is 0,1 or 2;
and, other than the ring substitution defined by G, >A3-B3- and Rp, each ring system may be
optionally further substituted on a carbon atom not adjacent to the link at >A3- by up to two
substituents independently selected from (l-4C)alkyl, fluoro(l-4C)alkyl (including
trifluoromethyl), (l-4C)alkyl-thio-(l-4C)alkyl, hydroxy-(l-4C)alkyl, amino, arnino-(l-
4C)aIkyl, (l-4C)alkanoylamino, (l-4C)alkanoylamino-(l-4C)alkyl, carboxy, (1-
4C)alkoxycarbonyl, AR-oxymethyl, AR-thiomethyl, oxo (=0) (other than when G is >N-Rc
and Re is group (Rc2) defined hereinbefore) or independently selected from Re; and also
hydroxy or halo (the last two optional substituents only when G is -0- or -S-);
wherein AR is optionally substituted phenyl, optionally substituted phenyl(l-4C)alkyl,
optionally substituted naphthyl, optionally substituted 5- or 6-membered heteroaryl;
an optionally substituted 5/6 or 6/6 bicyclic heteroaryl ring system, in which the bicyclic
heteroaryl ring systems may be linked via an atom in either of the rings comprising the
bicyclic system, and wherein both the mono- and bicyclic heteroaryl ring systems are linked
via a ring carbon atom and may be (partially) hydrogenated; and
Re is selected from groups (Rcl) to (Rc5) defined in claim 1.
3. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, as claimed in claims 1 and 2, in which the optional substituents in AR are independently selected from halo, (l-4C)alkyl, hydroxy, nitro, carbamoyl, (1-4Cfzlkylc£rtttinoyI, di-({l-4C}a&y{)carbamoyl, cyaao, trifluoromethyl, triftuorametboxy, amino, (l-4C)alkylamino, di((l-4C)alkyl)amino, (l-4C)alkyl S(O) - (q is 0,1 or 2), carboxy,
(l-4C)alkoxycarbonyl, (2-4C)atbnyl, (2-4C)alkynyl, (l-4C)alkanoyl, (l-4C)alkoxy, (1-4C)alkylS(0) 2amino, (l-4C)alkanoylamino, benzoylamino, benzoyl, phenyl (optionally

substituted by up to three substituents selected from halo, (l-4C)alkoxy
or cyano), furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine,
pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, thiophene,
hydroxyimino (l-4C)alkyl, (l-4C)alkoxyimino(l-4C)alkyl, hydroxy-(l-
4C)alkyl, halo-(l-4C)alkyl, nitro(l-4C)alkyl, amino(l-4C)alkyl, cyano(l-
4C)alkyl, (l-4C)alkanesulfonamido, aminosulfonyl, (1-
4C)alkylaminosulfonyl and di-((l-4C)alkyl)aminosulfonyl.
4. A compound of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, as claimed in any of claims 1 to 3, wherein the groups defined in (TCa) to (TCc), and (TCI) to (TC4) are defined by formulae (TC5) to (TC11) :-

wherein Re is as defined in claim 1.
5. A compound of the formula (IC), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, as claimed in any of claims 1 to

wherein HET is as claimed in any of claims 1 to 4; R2 and R3 are
independently hydrogen or_fluoro; Rpl and Rp2 are
independently hydrogen, AR-oxymethyl or AR-thiomethyl [wherein AR is phenyl, phenyl-(l-4C)alkyl, naphthyl, furan, pyrrole, pyrazole, imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole or thiophene], (l-4C)alkyl, carboxy, (1-4C)alkoxycarbonyl, hydroxymethyl, (l-4C)aIkoxymethyl or carbamoyl and Rep is cyano, pyrimidin- 2-yl, 2-cyanoethenyl, 2-cyano-2-((l-4C)alkyl)ethenyl or Rep is of the formula R10PCO-, R10PSO2- or RIOPCS-{wherein R10P is hydrogen, (l-5C)alkyl [optionally substituted by one or more groups each independently selected from hydroxy and amino, or optionally monosubstituted by [l-4C]alkoxy, (l-4C)alkylS(0)q-, (1-4C)alkylamino, (l-4C)alkanoyl, naphthoxy, (2-6C)alkanoylamino or (1-4C)alkylS(0)pNH- wherein p is 1 or 2 and q is 0, 1 or 2], imidazole, triazole, pyrimidine, pyridazine, pyridine, isoxazole, oxazole, isothiazole, thiazole, pyridoimidazole, pyrimidoimidazole, quinoxaline, quinazoline, phthalazine, cinnoline or naphthyridine, or R10P is of the formula RHP C(0)0(l-6C)alkyl wherein RUP is (l-6C)alkyI}, or Rep is of the formula RfC(=0)C(=0)- wherein Rf is (l-6C)alkoxy.
6. A compound of the formula (IC), or a pharmaceutically-acceptable salt, or an in-uifo-hydrolysable ester thereof, as claimed in any of claims 1 to

5, wherein HET is triazole or tetrazole.
7. A compound, as claimed in any of claims 1 to 6, being ((5R)-3-(4-(l -(2-Hydroxyacetyl)-1,2,5,6-tetrahydropyridin-4-yl)-3,5-difluorophenyl) -5- (1,2,3-traizol-1 -ylmethyl) oxazolidin-2-one; ((5R)-3-(4-(l-(2S)-2,3-Dihydroxypropionyl)-l,2,5,6-tetrahydropyridin-4-yl)-3,5-difluoro phenyl)-5-(l,2,3-triazol-l-ylmethyl)oxazolidin-2-one; (5R)-3-(4-( 1 -(2-Hydroxyacetyl)-1,2,5,6-te1xahydropyridin-4-yl)-3-fluorophenyl)-5-(l ,2,3-triazol-l-ylmethyl)oxazolidin- 2-one; (5R)-3-(4-(l-(2S)-2,3-Dihydroxypropionyl)-l,2,5,6-tetrahydropyridin-4-yl)-3-fluorophenyl)- 5-(l,2,3-triazol-l-ylmethyl)oxazolidin-2-one; or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof.
8. A compound, as claimed in claim 1, being
(5R)-3-(3,5-Difluoro-4-(3,6-dihydro-l,l-dioxo-2H-thiopyran-4-yl)phenyl)-5-( 1,2,3-triazol-1 -ylmethyl)oxazolidin-2-one.
9. A process for the preparation of a compound of the formula (I) as
claimed in claim 1, or pharmaceutically-acceptable salts or in vivo
hydrolysable esters thereof, which comprises of (a) to (d) :-
(a) modification of a substituent in or introduction of a substituent into another compound of formula (I);.
(b) reaction of a compound of formula (II) :

III
wherein Y is a displaceable group (which may be preformed such as
chloro or mesylate, or generated in-situ, for example under Mitsunobu
conditions)
with a compound of the formula (III) :
HET
(III) wherein HET is HET -H free-base form or HET -anion formed from the free base form; or (c) reaction of a compound of the formula (IV) :

(IV) wherein Z is an isocyanate, amine or urethane group with an epoxide of the formula (V) :

(V)
(d) for HET as 1,2,3-triazole cycloaddition via the azide (wherein Y in (II) is azide); and thereafter if necessary: (i) removing any protecting groups; (ii) forming a pharmaceutically-acceptable salt; (iii) forming an in-vivo hydrolysable ester.
10. A pharmaceutical composition which comprises a compound of the

formula [I] as claimed in any one of claims 1 to 8, or a pharmaceutically-
acceptable salt or an in-vivo hydrolysable ester thereof, and a
pharmaceutically-acceptable diluent or carrier.
Dated this Ist day of October, 2002.
[ JAYANTA PAL]
OF REMRRY &SAGAR
ATTORNEY FOR THE APPLICANTS

Documents:

in-pct-2002-01363-mum-abstract(27-03-2006).doc

in-pct-2002-01363-mum-abstract(27-03-2006).pdf

in-pct-2002-01363-mum-cancelled pages(27-03-2006).pdf

in-pct-2002-01363-mum-claims(granted)-(27-03-2006).doc

in-pct-2002-01363-mum-claims(granted)-(27-03-2006).pdf

in-pct-2002-01363-mum-correspondence(12-04-2006).pdf

in-pct-2002-01363-mum-correspondence(ipo)-(21-08-2007).pdf

in-pct-2002-01363-mum-form 18(04-03-2005).pdf

in-pct-2002-01363-mum-form 1a(01-10-2002).pdf

in-pct-2002-01363-mum-form 2(granted)-(27-03-2006).doc

in-pct-2002-01363-mum-form 2(granted)-(27-03-2006).pdf

in-pct-2002-01363-mum-form 3(01-10-2002).pdf

in-pct-2002-01363-mum-form 3(27-03-2006).pdf

in-pct-2002-01363-mum-form 4(16-01-2006).pdf

in-pct-2002-01363-mum-form 5(01-10-2002).pdf

in-pct-2002-01363-mum-form 5(27-03-2006).pdf

in-pct-2002-01363-mum-form-pct-ipea-409(01-10-2002).pdf

in-pct-2002-01363-mum-form-pct-isr-210(01-10-2002).pdf

in-pct-2002-01363-mum-power of authority(01-10-2002).pdf

in-pct-2002-01363-mum-power of authority(27-03-2006).pdf

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Patent Number

209138

Indian Patent Application Number

IN/PCT/2002/01363/MUM

PG Journal Number

35/2007

Publication Date

31-Aug-2007

Grant Date

21-Aug-2007

Date of Filing

01-Oct-2002

Name of Patentee

ASTRAZENECA AB

Applicant Address

S-151 85 SODERTALJE, SWEDEN

Inventors:

#	Inventor's Name	Inventor's Address
1	MICHAEL BARRY GRAVESTOCK	35 GATEHOUSE DRIVE, WALTHAM, MA 02451, USA
2	MICHAEL JOHN BETTS	ALDERLEY PARK, MACCLESFIELD, CHESHIRE SK10 4TG, ENGLAND
3	DAVID ALAN GRIFFIN	FERNHURST, HASELMARE, SURREY GU27 3JE, ENGLAND.
4	IAN RICHARD MATTHEWS	FERNHURST, HASELMERE, SURREY GU27 3JE, ENGLAND.

PCT International Classification Number

A61K 31/42

PCT International Application Number

PCT/GB01/01815

PCT International Filing date

2001-04-23

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	0009803.8	2000-04-25	U.K.