Title of Invention	4-PYRROLIDINO-PHENYL-BENZYL ETHER DERIVATIVES
Abstract	The invention relates to racemic or enantiomerically pure 4-pyrrolidino derivatives of formula (I), processes for their preparation, pharmaceutical compositions comprising said derivatives, and their use in the prevention and treatment of illness, e.g. which are mediated by monoamine oxidase B inhibitors, in particular Alzheimer's disease or senile dementia. ABSTRACT 419/CHENP/2005 4-PYRROLIDINO-PHENYL-BENZYL ETHER DERIVATIVES The invention relates to racemes or enantiomerically pure 4-pyrrolidino derivatives, processes for their preparation, pharmaceutical compositions comprising said derivatives, and their use in the prevention and treatment of illness e.g. which are mediated by monoamine oxidase B inhibitors in particular Alzheimer's disease or senile dementia.

Title of Invention

4-PYRROLIDINO-PHENYL-BENZYL ETHER DERIVATIVES

Abstract

The invention relates to racemic or enantiomerically pure 4-pyrrolidino derivatives of formula (I), processes for their preparation, pharmaceutical compositions comprising said derivatives, and their use in the prevention and treatment of illness, e.g. which are mediated by monoamine oxidase B inhibitors, in particular Alzheimer's disease or senile dementia. ABSTRACT 419/CHENP/2005 4-PYRROLIDINO-PHENYL-BENZYL ETHER DERIVATIVES The invention relates to racemes or enantiomerically pure 4-pyrrolidino derivatives, processes for their preparation, pharmaceutical compositions comprising said derivatives, and their use in the prevention and treatment of illness e.g. which are mediated by monoamine oxidase B inhibitors in particular Alzheimer's disease or senile dementia.

Full Text	The invention relates to 4-pyrrolidino -phenyl-benzyl ether derivatives- In particular racemes or enantiomerically pure 4-pyrrolidino derivatives, processes for their preparation, pharmaceutical compositions comprising said derivatives, and their use in the prevention and treatment of illness. More particularly, the present invention relates to compounds of the formula I R" , R"', R"" and R independently from each other are selected from the group consisting of hydrogen and halogen; R is hydrogen; R’ is-CONHR’-CH2CN,-CNo’-NHR’; R is hydrogen or Ci-Cs-alkyI; R’ is-C0-(Ci-C6)-alkyl or-S02-(Ci-C6)-alkyl; and n is 0,1,2 or 3; as well as individual isomers, racemic or non-racemic mixtures thereof. It has been found that the compounds of general formula I and P as well as individual isomers, racemic or non-racemic mixtures thereof (hereinafter: Active Compounds) are selective monoamine oxidase B inhibitors. Monoamine oxidase (MAO, EC 1.4.3.4) is a flaking-containing enzyme responsible for the oxidative deamination of endogenouslnonoamine neurotransmitters such as dopamine, serotonin, adrenaline, or noradrenaline, and trace amines, e.g. phenylethyl-amine, as wet as a number of amine xenobiotics. The enzyme exists in two forms, MAO-A and A'lAO-B, encoded by different genes [Bach et al, Proc. Natl. Acad. Sci. USA 85:4934-4938 (1988)] and differing in tissue distribution, structure and substrate specificity. MAO-A has higher affinity for serotonin, octopamine, adrenaline, and noradrenaline; whereas the natural substrates for MAO-B are phenylethylamine and t’'ramine. Dopamine is thought to be oxidised by both isoforms. MAO-B is widely distributed in several organs including brain [Cesura and Pletscher, Prog. Drug Research 38:171-297 (1992)]. Brain MAO-B activity appears to increase with age. This increase has been attributed to the gliosis associated with aging [Fowler et al., J. Neural. Transm. 49:1-20 (1980)]. Additionally, MAO-B activity is significantly higher in the brains of patients with Alzheimer's disease [Dostert et al, Bio-chem. Pharmacol. 38:555-561 (1989)] and it has been found to be highly expressed in astrocytes around senile plaques [Saura et al., Neuroscience 70:755-774 (1994)]. In this context, since oxidative deamination of primary monoamines by MAO produces NH3, aldehydes and H2O2, agents with established or potential toxicity, it is suggested that there is a rationale for the use of selective MAO-B inhibitors for the treatment of dementia and Parkinson's disease. Inhibition of MAO-B causes a reduction in the enzymatic inactivation of dopamine and thus prolongation of the availability of the neurotransmitter in dopa¬minergic neurons. The degeneration processes associated with age and Alzheimer's and Parkinson's diseases may also be attributed to oxidative stress due to increased MAO acti¬vity and consequent increased formation of H2O2 by MAO-B. Therefore, MAO-B inhibi- tors may act by both reducing the formation of oxygen radicals and elevating the levels of monoamines in the brain. Given the implication of MAO-B in the neurological disorders mentioned above, there is considerable interest to obtain potent and selective inhibitors that would permit control over this enzymatic activity. The pharmacology of some known MAO-B inhibitors is for example discussed by Bentue-Ferrer et al. [CNS Drugs 6:217-236 (1996)]. Whereas a major limitation of irreversible and non-selective MAO inhibitor activity isthe need to observe dietary precautions due to the risk of inducing a hypertensive crisis when dietary tyramine is ingested, as well as the potential for interactions with other medications [Gardner et al., J. Clin. Psychiatry 57:99-104 (1996)], these adverse events are of less concern with rever¬sible and selective MAO inhibitors, in particular of MAO-B. Thus, there is a need for MAO-B inhibitors with a high selectivity and without the adverse side-effects typical of irreversible MAO inhibitors with low selectivity for the en2yme. The following definitions of general terms used herein apply irrespective of whether the terms in question appear alone or in combination. It must be noted that, as used in the specification and the appended claims, the singular forms "a", "an," and "the" include plural forms unless the context clearly dictates otherwise. The term "(Ci-C6)-alkyr' used in the present application denotes straight-chain or branched saturated hydrocarbon residues with 1 to 6 carbon atoms, such as methyl, ethyl, n-propyl, i-propyl, n-butyl, sec-butyl, t-butyl, and the like, preferably with 1 to 3 carbon atoms. Accordingly, the term "(Ci-C3)-aIkyr' means a straight-chain or branched saturated hydrocarbon residue with 1 to 3 carbon atoms. The term "halogen" denotes fluorine, chlorine, bromine and iodine. "Halogen-(Ci-C6)-alkyr or "halogen-(CrC6)-alkoxy" means the lower alkyl residue or lower alkoxy residue, respectively, as defined herein substituted in any position with one or more halogen atoms as defined herein. Examples of halogenalkyl residues include, but are not limited to, 1,2-difluoropropyl, 1,2-dichloropropyl, trifluoromethyl, 2,2,2-trifluoro-ethyl, 2,2,2-trichloroethyl, and 3,3,3-trifluoropropyl,~and the like. "Halogenalkoxy" in¬cludes trifluoromethyloxy. "(Ci-C6)-AIkoxy" means the residue -O-R, wherein R is a lower alkyl residue as defined herein. Examples of alkoxy radicals include, but are not limited to, methoxy, ethoxy, iso- ■ propoxy, and the like. "Pharmaceutically acceptable salts" of a compound means salts that are pharmaceutically acceptable, which are generally safe, non-toxic, and neither biologically nor otherwise un¬desirable, and that possess the desired pharmacological activity of the parent compound. These salts are derived from dn inorganic or organic acid or base. If possible, compounds of formula I maybe converted into pharmaceutically acceptable salts. It should be understood that pharmaceutically acceptable salts are included in the present invention. In another embodiment the present invention provides compounds of formula F, wherein R’ is hydrogen and R* is selected from the group consisting of-CONHR’, -CH2CN, or -CN. Those compounds of formula I, wherein R is -CONHR’ and R’ is hydrogen or (C1-C3)- alkyl, are especially preferred. Examples of such compounds are (RS)-l-[4-(3-fluoro-benzyloxy)-phenyl] -2-oxO-pyrrolidine-3-carboxylic acid methylamide; (RS)-l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide; (RS)-l-[4-(4-fluoro-ben2yloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxyhc acid amide; (RS)-l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylicacid methylamide; (RS)-2-oxo-l-[4-(4-tri£luoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxyHcacid amide; and (RS)-2-oxo-1 -[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxyhc acid methylamide. Another group of preferred compounds of formula P are those, wherein R* is -CN. (RS)--l-(4-benzylox}’-phenyl)-2-oxo-pyrrolidine-3-carbonitrile is an example of such a compound. Also preferred are compounds of formula F, wherein R’ is hydrogen, R is -NHR and R is -C0-(Ci-C6)-alkyl or -S02-(Ci-C6)-alkyl. Examples of such compounds are (S)-N-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrohdin-3-yl]-acetamideand(S)-N-[l-(4-benzylox)’-phenyl)-2-oxo-pyrrolidin-3-yl]-methanesulfonamide. Compounds of formula F maybe substituted by n R’ selected from the group consisting of halogen, halogen-(CrC6)-alkyl, cyano, (Ci-C6)-aIkoxy or halogen-(Ci-C6)-alkoxy, wherein n denotes an integer selected from 0, 1, 2 and 3. Preferably n is 1 or 2. Preferred compounds of formula F are those, wherein R’ is halogen or halogen-(Ci-C6)-alkyl. Especially preferred are those compounds of formula F, wherein R is fluorine, chlorine or trifluoromethyl. W’ere the compounds of formula P are substituted by two or three R\ each R can be the same or different. In one embodiment the invention provides compounds of formula I wherein -X-Y- is -CH2-O-. In another embodiment the invention provides compounds of formula I where¬in -X-Y- is -CH2-CH2- or -CH=CH-. In one embodiment the invention provides compounds of formutla I wherein R’ R’'‘ and R ■ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, cyano, methoxy or halogen-methoxy. In another embodi¬ment the present invention provides compounds of formula I wherein R\ R'"' and R’'‘ are halogen, e.g. fluoro, e.g. 2,4,6-trifluoro, 2,4,5-trifluoro, 2,3,6-trifluoro, 2,3,4-trifluoro or 3,4,5-trifluoro. In still another embodiment the present invention provides compounds of formula I wherein R'"'‘ is hydrogen and R’ and R’' independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-C6)-allcyl,' halogen-(Ci-Q)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(CrC6)-alkoxy. In still another embodiment the present invention provides compounds of formula I wherein R’'‘ is hydrogen and R’ and R’'‘ independently from each other are selected from the group consisting of halogen and (Ci-C6)-alkyl. In stiU another embodiment the present invention provides compounds of formula I wherein R’'‘ is hydrogen, R’'‘ is halogen and R’ is halogen or (Ci-C6)-alkyl. In still another embodiment the present invention provides compounds of formula I wherein R’'‘ and R’'‘ are hydrogen and R’ is halogen, (Ci-C6)-alkyl, halogen-(Ci-C6)-alkyl, cyano, (Ci-C6)-aIkoxy or halogen-(Ci-C6)-aIkoxy. In still another embodiment the present inven¬tion provides compounds of formula I wherein R’'‘ and R’'‘ are hydrogen and R is halo¬gen, methyl, halogenmethyl, cyano, methoxy or halogen-methoxy. In still another embodi¬ment the present invention provides compounds of formula I wherein R ' and R ■' are hydrogen and R’ is fluoro, e.g. 3-fluoro or 4-fluoro, chloro, e.g. 3-chloro, halogenmethyl, e.g. 3-trifluoromethyl or 4-trifluoromethyl, cyano, methoxy, e.g. 2-methoxy, 3-methoxy or 4-methoxy, or halogen-methoxy, e.g. 3-trifluoromethoxy. In another embodiment the present invention provides compounds of formula I wherein R , R ' and R " are hydrogen. In one embodiment the present invention provides compounds of formula I wherein R , R’’andR’’ are hydrogen. In one embodiment the present invention provides compounds of formula I wherein R' is hydrogen. In one embodiment the present invention provides compounds of formula I wherein R* is -CONHR , wherein R’ is hydrogen or (Ci-C3)-allcyl. In another embodiment the present invention provides compounds of formula I wherein R’ is -CONHR’, wherein R’ is hydrogen or methyl. In one embodiment the present invention provides compounds of formula I wherein R* is -CN. In one embodiment the present invention provides compounds of formula I wherein R is -NHR’ wherein R’ is -CO-H, -CO-(Ci-C6)-alkyl, -CO-halogen-(Ci-C3)-alkyl, -CO-O-(CrC3)-allcyl, -CO-NH2 or -S02-(Ci-C6)-alkyl. In another embodiment the present invention provides compounds of formula I wherein R’ is -NHR’, wherein R is -CO-H, -C0-(CrC6)-alkyl, -C0-0-(Ci-C3)-alk)'-l, -CO-NH2 or -S02-(Ci-C6)-alk)d. In still another embodiment the present invention provides compounds of formula I wherein R is -NHR’ wherein R’ is -CO-H, -CO-methyl, -CO-O-methyl, -CO-NHo or -SOz-methyl. In one aspect the present invention provides compounds of formula I wherein the compounds have (S)-configuration. In one aspect the present invention provides compounds of formula I wherein the compounds have (R)-configuration. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’ R’'‘ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, cyano, methoxy or halogen-methoxy; R’’ R’’ and R’’ are hydrogen; R’" is hydrogen and R’ is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-alkyl. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’'‘ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, q'‘ano, methoxy or halogen-methoxy; R , R " and R are hydrogen; R is hydrogen and R is -CN. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’"‘ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, cyano, methoxy or halogen-methox}'; R , R"" and R are hydrogen; R is hydrogen and R is -NHR , wherein R is -C0-H,-C0-(Ci-C6)-alkyl, -CO-halogen-(Ci-C3)-alkyl, -C0-0-(Ci-C3)-alkyl, -CO-NH2 or -S02-(Ci-C6)-alkyl. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-’ is hydrogen and R’ and R’"‘ independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-CoO-alkyl, halogen-(Ci-C6)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(Ci-C6)-alkoxy; R’’ R’’ and R’’ are hydrogen; R"" is hydrogen; and R* is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-aIkyl. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’' and R’'‘ are hydrogen and R’ is halogen, (Ci-C6)-alkyl, halogen-CCi-Ce)-alkyl, cyano, (Ci-C6)-alkox7 or halogen-(Ci-C6)-alkoxy; R’\ R’" and R’’ are hydrogen; R’’ is hydrogen; and R' is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-allcyl. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’-’ and R’"‘ are hydrogen; R’\ R’’ and R’’ are hydrogen; R’’ is hydrogen; and R’ is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-alkyL In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R '‘ is hydrogen and R and R ' independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-C6)-aIkyl, halogen-(Ci-C6)-aIkyl, cyano, (Gi-C6)-allcoxy or halogen-(Ci-C6)-aIkoxy; R'‘‘ R’’ and R’’ are hydrogen; R’* is hydrogen; and R* is -CN. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’"‘ and R’-’ are hydrogen and R' is halogen, (Ci-C6)-alkyl, halogen-CCi-Ce)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(Ci-C6)-alkoxy; R’\ R’’ and R"‘ are hydrogen; R’* is hydrogen; and R’ is -CN. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R', R’-’ and R’'‘ are hydrogen; R’’ R’’ and R’-' are hydrogen; R'‘ is hydrogen; andRis-CN. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’'‘ is hydrogen and R’ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-C6)-alkyl, halogen-(Ci-C6)-aIkyl, cyano, (Ci-C6)-alkox7 or halogen-(CrC6)-alkoxy; R'‘ R’" and R’"‘ are hydrogen; R’'‘ is hydrogen; and R is -NHR’ wherein R’ is -CO-H, -C0-(Ci-C6)-alkyl, -CO-halogen-(Ci-C3)-alkTl, -C0-0-(Ci-C3)-alkyl, -CO-NH2 or -S02-(Ci-C6)-alkyl. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-’ andR’-' are hydrogen and R’ is halogen, (Ci-C6)-aIkyl, halogen-(Ci-Ce)- allcyi, cyano, (Ci-Cgj-alkoxy or halogen-(CrC6)-alkoxy; R’\ R~’ and R'‘ are hydrogen; R’' is hydrogen; and R* is -NHR’ wherein R’ is -CO-H, -C0-(Ci-C6)-alkyl, -CO-halogen-(CrC3)-alkyl, -C0-O-(CrC3)-alkyl, -CO-NH2 or -S02-(Ci-C6)-alkyl. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’-' and R’-’ are hydrogen; B}\ R’’ and R’’ are hydrogen; R’’ is hydrogen; and R’ is -NHR’ wherein R’ is -CO-H, -C0-(Ci-C6)-aIkyI, -CO-halogen-CCi-QO-alkyI, -C0-0-(Ci-C3)-allcyl, -CO-NH2 or -S02-(CrC6)-alkyl. In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-' and R’'‘ are hydrogen and R’ is halogen; R’\ R’’ and R’’ are hydrogen; R-'‘ is hydrogen; and R* is -NHR’ wherein R’ is -C0-(Ci-C6)-alkyl. In another embodi¬ment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-\ R'-’ R’\ R’\ R-’ and R’’ are hydrogen; R’ is halogen; and R’ is -NHR’ wherein R’ is -CO-methyl. Examples of compounds of formula I include compounds selected from (RS)-l-(4-benzyloxy-phenyl)-2-oxo-p)Trrolidine-3-carbonitrile, (RS)-l-[4-(3-fluoro-henzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid methyl-amide, (RS)-l-[4-(3-f[uoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide, (RS)-l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxyhc acid amide, (RS)-l-[4-(4-fluoro-ben2yloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid methyl-amide, (RS)-2-oxo-l- [4-(4-trifluoromethyl-benzyloxy)-phenyl] -pyrrohdine-3-carboxylic acid amide, (RS)-2-oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrroHdine-3-carboxyhcacid methylamide, (S)-N-[l-(4-benzylox7-phenyl)-2-oxo-pyrroHdin-3-yl]-acetamide, (S)-N-[l-(4-benzyloxy-phenyl)-2-oxo-pyrroHdin-3-yl]-methanesulfonamide, (S)-N-{l-[4-(3-fluoro-benzylox7)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide, (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide, (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-methanesulfonamide, (S)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-methanesulfonamide, (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid methyl ester, (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-formamide, (S)-N-{ 1-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-formamide, (R)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-urea, (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-urea, (S)-N-{ 1-(S)- [4-(4-fluoro-benzyloxy)-phenyl] -2-oxo-pyrroIidin-3-yl}-acetamide, (S)-N-{l-(S)-[4-(2,6-difiuoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-acetamideand (S)-N-{ 1-[4-(3,4-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide. In one embodiment the present invention provides a process for the preparation of compounds of formula I wherein (a)RSsCONHR’ comprising reacting a compound of formula II (11) wherein R\ R’\ R’'‘ R’\ R’\ R’’ R’’ R’ X and Y have the meanings as defined above and R'' is hydrogen or (Ci-C6)-alkyl, with an amine of formula H2N-R’, wherein R’ has the above meaning; (b) R is CN comprising reacting a compound of formula III (HI) wherein R\ R’-\ R’•’ R’\ R’\ R"‘ R’’ R’ X and Y have the meanings as defined above and Hal is halogen, with a cyanide salt; or (c) R* is NHR’ comprising reacting a compound of formula IV R= 23 , ( (IV) wherein R\ R’-\ R’-\ R-\ R’\ R-\ R-’ R’ X and Y have the meanings as defined above, with an acyl donating agent of formula Z-C0-(G]-C6)-alkyl, Z-CO-halogen-(Ci-C3)-alkyl, Z-CO-0-(Ci-C3)-alkyl, or Z-S02-(Ci-C3)-aIkyl wherein Z is an activating group, e.g. a halogen or anhydride , or with an isocyanate. The compounds of general formula I* can be manufactured by reacting a compound of formula IF COOH wherein R\ R’\ R’\ R’’ R’'‘ and n have the above meanmgs with an amine of formxila H2N-R’, wherein R’ has the above meaning, to obtain a compound of formula la"* (la’) or, alternatively, reducing a compound of formula IF to the corresponding alcohol of formula IIP (III) and reacting this compound with a cyanide salt to obtain a compound of formula lb (lb) or, alternatively, reacting a compound of formula IV" (iv’) wherein X is halogen, with a cyanide salt, to obtain a compound of formula Ic'" ilc) or, alternatively, reacting a compound of formula V'' (V) with an acylating agent of formula Y-C0-(Ci-C6)-aIlcyl or Y'-S02-(Ci-C6)-alkyl, wherein Y and Y' represent an activating group, e.g. a halogen, to obtain a compound of formula Id* (Id) wherein R has the above meanings. In accordance with the present invention, scheme 1 shows examplary routes to com¬pounds of the formula I, all starting from a compound of formula V. The reaction of a compound of formula V with a compound of formula VI [Ikuta et al., J. Med. Chem. 30:1995 (1987)] to obtain the intermediate of formula Ilia, maybe in inert solvents like dichloromethane, ethyl acetate or ethers in the presence of a base like triethylamine or carbonate and at a temperature in the range of from 0°C to 25°C. Cyclisation of the intermediate 2,4-dihalo-N-acyl derivative to the p’Trolidone Ilia may be with bases like sodium or potassium hydroxide in inert solvents like dichloromethane or ethers at a temperature of from 0°C to 25°C. Intermediates II wherein R* is H, i.e. compounds of formula Ila, are prepared by reacting a compound of formula V with 6,6-dimethyl-5,7- dioxa-spiro[2,5]octane-4,8-dione, as described by Danishefsky et al. [J. Amer.Chem. Soc. 97:3239(1975)]. Scheme 1 hal 1) hal-CHjCHj-CH ‘hal Another method to prepare compounds of formula I involves cross-coupling reactions of arylstannanes [Lam et al., Tetrahedron Lett. 43:3091 (2002)], arylboronates [Lam et al., Synlett 5:674 (2000); Chan et al, Tetrahedron Lett. 39:2933 (1998)] or aryl haUdes [Buch-wald et al., J. Amer. Chem. Soc. 118:7215 (1996)] with the corresponding pyrroHdones (scheme 2). Scheme 2 R’-’' ' VIII wherein LG is halogen, e.g. CI, Br or I, or SnRs or B(0H)2. In accordance with the present invention, a possibility to prepare compounds of general formula V, wherein -X-Y- is -CH2-O-, i.e. compounds of formula Va, is shown in scheme 3: The intermediates of formula XII are accessible through nucleophilic substitution of aromatic nitro compounds of formula XI containing p-substituted leaving groups with benzylic alcohols of formula X. Leaving groups in para-position can be, e.g., halogens (F, CI, Br, I), tosylates, mesylates or triflates. These substitution reactions can be conducted neat or in inert solvents like for example toluene or xylene. A preferred reaction temperature is in the range of from 50°C to 150°C. Alternatively, compounds of formula XII can be prepared by WiEiamson-ether synthesis, starting from p-nitrophenols XIV and benzylic halides, tosylates, mesylates or triflates of formula XIII. Bases used can be, e.g. alcoholates or carbonates (sodium, potassium or cesium carbonate). Examples for solvents include lower alcohols, acetonitrile or lower ketones at a temperature in the range of from 20°C to reflux temperature. Another approach is the Mitsunobu-coupling of benzylic alcohols with p-nitrophenols. The reaction is done as usual in inert solvents like for example diethyl ether or tetrahydrofurane, using dialkyl-azo-dicarboxylates in the presence of phosphines (for example tributyl- or triphenyl-phosphine). The key intermediates of formula XII are reduced to the amino compounds of formula Va using catalytic hydrogenation, like, e.g. using platinum on charcoal as the catalyst in lower alcohols, ethyl acetate or tetrahydrofurane. An alternative is the reduction of the nitro-group by metals lilce iron, tin, or zinc in acidic media like diluted hydrochloric acid or acetic acid. Metals can also be replaced by metal salts lilce, e.g., tin-(II)-chloride). Scheme 3 R!'‘ .CH,OH ,_r’rv’°"‘'-° i.2 XIII R XIV + wherein LG is a leaving group, e.g. halogen and OTf, or OH (for Mitsunobu-coupling). In accordance with the present invention, a possibility to prepare the intermediates of formula Vb (wherein -X-Y- is -CH=CH-) and Vc (wherein -X-Y- is -CH2-CH2-) is shown in scheme 4: The intermediates of formula XVII are accessible by olefmation reac¬tion of optionally substituted aromatic aldehydes of formula XV with dialkyl (4-nitro-benzyl)-phosphonates of formula XVI in the presence of a base, like e.g. sodium hydride, yielding the corresponding nitro-olefins of formula XVII. Scheme 4 23 O The key intermediates of formula XVII can be reduced selectively to the amino-olefins of formula Vb using catalytic hydrogenation like e.g. using platinum on charcoal as the cata¬lyst in lower alcohols, ethyl acetate or tetrahydrofiirane as the solvent, or, by metals or metal salts, lilce e.g. tin-(II)-chloride. The amino derivatives of formula Vc can be obtained directly fi-om the nitro derivatives of formula XVII or fi:om the amino-olefins of formula Vb by hydrogenation using palladium on charcoal as the catalyst in lower alcohols, ethyl acetate or tetrahydrofiirane as the solvent. Intermediates II can be transformed into compounds of formula I using standard procedures. The acids II are activated via acid chloride (thionyl chloride or oxalyl chloride) or with DCC, EDC etc. and subsequently coupled with the amine R’-NH2. Alternatively, the corresponding alkyiesters can be transformed to intermediates II by aminolysis by ammes of formula R’-NH2. Intermediates III can be transformed into the desired compounds I wherein R is CN, i.e. compounds of formula lb, by reaction with sodium or potassium cyanide in solvents like N,N-dimethylformamide, acetone or acetonitrile at a temperature in the range of from 20°C to 140°C. Catalytic amounts of sodium or potassium iodide can be added to speed up "the"reaction (scheme 5). Scheme 5 III Compounds of formula IV can be obtained starting from acid derivatives of formula II by nucleophilic migrations from a carbon to a nitrogen atom, such as e.g. by Hofmann or Curtius rearrangement, via the formation of the corresponding isocyanate and its treat¬ment with suitable alcohols delivering the protected amino group, methods known per se from the literature (scheme 6). For the treatment of the intermediate isocyanate, alcohols are selected which yield the typical carbamates used as amine protecting groups, such as e.g. tert-butoxycarbonyl, benzyloxycarbonyl, or fluorenylmethoxycarbonyl. Their cleavage to the amine follows the protocols which are well known in the literature. The farther transformation to compounds of formula I can be performed by standard procedures, such as e.g. by reaction with activated acyl derivatives, e.g. acyl halogenides or anhydrides, or by condensation reactions of the acid using e.g. carbodiimides as condensation reagent, or by isocyanates. Scheme 6 NH-PG »- IV For the preparation of enantiopure derivatives of formula IV, an alternative route can be followed (scheme 7). Basically, the protocol follows the conditions described by Freidinger et al. [J. Org. Chem. 47:104-109 (1982)] where the aniline derivative of formula V is acyla-ted by an N-protected methionine derivative in its racemic or optically active form by standard conditions of condensation reactions to give compounds of formula XIX. Methylation with methyliodide or trimethyl-sulfonium or trimethylsulfoxonium salts and treatment of the resulting dimethyl-sulfonium salt with base, such as e.g. sodium hydride or lithium or potassium bis(trimethylsilyl)amide, in solvents inert under these conditions, e.g. THF, dichloromethane or N,N-dimethylformamide, yield the cyclised N-protected product of formula XX. Another variation of this cyclisation procedure is described in EP 985,665 which refers to a process for the preparation of 3-amino-2-oxo-pyrrolidines. Scheme 7 gXHg HOOC N H XX -X-Y- = -CH2-O-: R"' hydrogenolysis R’\X’’N’/~~-NH-PG XX -« I I _ alkylation HC'l’’’R’ ‘‘ NHR -X-Y-=-CH2-O-: I J , hydrogenolysis R’\’;!K’N’ HO V’ -° NHR" alkylation -R" Id In compounds of formula I or XX where -X-Y- has the meaning of-CHz-O-, the op¬tionally substituted benzyl residue can function as a transient group which can be cleaved by hydrogenolysis. The resulting phenols Id and XXa can then be re-alkylated by a dif¬ferent benzyl group under the aforementioned conditions. As known to those skilled in the art, this process is only possible on condition that R and PG are representing groups that are stable under the aforementioned reaction conditions for the hydrogenolysis and alkylation reaction. Compounds of general formula I can also exist in optical pure form. There ist the possibility to start with enantiopure compounds from the chiral pool, like e.g. (R)- or (S)-methionine. In other cases, separation into antipodes can be affected according methods known per se, either preferably at an early stage of the synthesis starting with compounds of formula II by salt formation with an optically active amine such as, for example, (-f-)- or (-)-l-phenylethylamine and separation of the diastereomeric salts by fractional crystallisation or preferably by derivatisation with a chiral auxiliary substance such as, for example, (+)- or (-)-2-butanol, (+)- or (-)-l-phenylethanol, or {+)- or (-)-menthol and separation of the diastereomeric products by chromatography and/or crystallisation and subsequent cleavage of the bond to the chiral auxiliary substance. In order to determine the absolute configuration of the pyrrolidinone derivative obtained, the pure diastereo-meric salts and derivatives can be analysed by conventional spectroscopic methods, with X-ray spectroscopy on single crystals being an especially suitable method. The Active Compounds are, as already mentioned above, monoamine oxidase B inhibitors and can be used for the treatment or prevention of diseases in which MAO-B inhibitors might be beneficial. These include acute and chronic neurological disorders, cognitive disorders and memory deficits. Treatable neurological disorders are for instance traumatic or chronic degenerative processes of the nervous system, such as Alzheimer's disease, other types of dementia, minimal cognitive impairment or Parkinson's disease. Other indica¬tions include psychiatric diseases such as depression, anxiety, panic attack, social phobia, schizophrenia, eating and metabolic disorders such as obesity, as well as the prevention and treatment of withdrawal syndromes induced by abuse of alcohol, nicotine and other addictive drugs. Other treatable indications maybe peripheral neuropathy caused by can¬cer chemotherapy (WO 97/33,572), reward deficiency syndrome (WO 01/34,172), or the treatment of multiple sclerosis (WO 96/40,095), and other neuroinflammatory diseases. The Active Compounds are especially useful for the treatment and prevention of Alzheimer's disease and senile dementia. The pharmacological activity of the compounds was tested using the following method: The cDNAs encoding human MAO-A and MAO-B were transiently transfected into EBNA cells using the procedure described by Schlaeger and Christensen [Cytotechnology 15:1-13 (1998)]. After transfection, cells were homogenised by means of a Polytron homogenizer in 20 mM Tris HCl buffer, pH 8.0, containing 0.5 mM EGTA and 0.5 mM phenylmethane-sulfonyl fluoride. Cell membranes were obtained by eentrifugation at 45,000 x g and, after two rinsing steps with 20 mM Tris HCl buffer, pH 8.0, containing 0.5 mM EGTA, mem¬branes were eventually re-suspended in the above buffer and aliquots stored at -80°C until use. MAO-A and MAO-B en2ymatic activity was assayed in 96-well-plates using a spectro-photometric assay adapted from the method described by Zhou and Panchuk-Voloshina [Analytical Biochemistry 253:169-174 (1997)]. Briefly, membrane ahquots were incubated in 0.1 M potassium phosphate buffer, pH 7.4, for 30 min at 37°C containing different con¬centrations of the compounds. After this period, the enzymatic reaction was started by the addition of the MAO substrate tyramine together with 1 U/ml horse-radish peroxidase (Roche Biochemicals) and 80 \|iM ]V-acet}d-3,7-dihydroxyphenoxazine (Amplex Red, Molecular Probes). The samples were further incubated for 30 min at 37°C in a final volume of 200 \|il and absorbance was then determined at a wavelength of 570 nm using a SpectraMax plate reader (Molecular Devices). Background (non-specific) absorbance was determined in the presence of 10 \|iM clorgyline for MAO-A or 10 jiM L-deprenyl for IvlAO-B. IC50 values were determined from inhibition curves obtained using nine inhibitor concentrations in dupHcate, by fitting data to a four parameter logistic equation using a computer program. The compounds of the present invention are specific MAO-B inhibitors. The IC50 values of preferred Active Compounds as measured in the assay described above are in the range of 1 \|iM or less, typically 0.1 \iM or less, and ideally 0.02 ‘M or less. The Active Compounds can be used as medicaments, e.g. in the form of pharmaceutical preparations. The pharmaceutical preparations can be administered orally, e.g. in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions. However, the administration can also be effected rectally, e.g. in the form of suppositories, or parenteraUy, e.g. in the form of injection solutions. The Active Compounds can be processed with pharmaceutically inert, inorganic or organic carriers for the production of pharmaceutical preparations. Lactose, corn starch or derivatives thereof, talc, stearic acid or its salts and the like can be used, for example, as such carriers for tablets, coated tablets, dragees and hard gelatine capsules. Suitable carriers for soft gelatine capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like; depending on the nature of the active substance no carriers are, how¬ever, usually required in the case of soft gelatine capsules. Suitable carriers for the produc¬tion of solutions and syrups are, for example, water, polyols, sucrose, invert sugar, glucose and the like. Adjuvants, such as alcohols, polyols, glycerol, vegetable oils and the like, can be used for aqueous injection solutions of water-soluble salts of Active Compounds, but as a rule are not necessary. Suitable carriers for suppositories are, for example, natural or hardened oils, waxes, fats, semi-liquid or liquid polyols and the like. In addition, the pharmaceutical preparations can contain preservatives, solubilizers, stabi¬lizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They may also contain other therapeutically valuable substances. As mentioned earlier, medicaments containing an Active Compound and a therapeutically inert excipient are also an object of the. present invention, as is a process for the pro¬duction of such medicaments which comprises bringing one or more Active Compound and, if desired, one or more other therapeutically valuable substances into a galenical dosage form together with one or more therapeutically inert carriers. The dosage can vary within wide limits and will, of course, be fitted to the individual requirements in each particular case. In general, the effective dosage for oral or parenteral administration is between 0.01-20 mg/kg/day, with a dosage of 0.1-10 mg/kg/day being preferred for all of the indications described. The daily dosage for an adult human being weighing 70 kg accordingly lies between 0.7-1400 mgper day, preferably between 7 and 700 mg per day. The following examples are provided for illustration of the invention. They should not be considered as limiting the scope of the invention, but merely as being representative there¬of The abbreviation „RT" means „room temperature". Example 1: (RS)-l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidine-3-carbonitrile a) (RS)-N-(4-Benzyloxy-phenyl)-2,4-dibromo-butyTamide A solution of 12.8 g (64.2 mmol) 4-benzyloxyaniline and 9.74 g (96.3 mmol) triethylamine in 125 ml dichloromethane is cooled to 0°C. 20.4 g (77.1 mmol) of 2,4-dibromobutyryl chloride [Ikuta et al., J. Med. Chem. 30:1995 (1987)] is slowly added over a period of 45 min. The reaction mixture is stirred for additional 15 min, then hydrolysed with 100 ml of water. The insoluble precipitate is filtered off and the organic phase is washed successively with a saturated solution of sodium hydrogen carbonate and water. After drying and eva¬poration, the crude product is subjected to chromatography (silica gel, dichloromethane) to yield 6.1 g (22 %) of a colorless soUd. Mp = 139.5-142 °C. b) (RS)-l-(4-Benzyloxy-phenyl)-3-bromo-pyrrolidin-2-one 6.1 g (14.3 mmol) (RS)-N-(4-benzyloxy-phenyl)-2,4-dibromo-butyTamide and 0.1 g of Dowex 2X10 are suspended in 50 ml dichloromethane. 7 ml of a 50% aqueous sodium hydroxide solution is slowly added under vigorous stirring. The resulting reaction mixture is stirred overnight at RT, then poured into 25 ml of cold water. The organic phase is separated, dried and evaporated. The crude material is recrystallised from ethyl acetate to yield 1.72 g (35 %) of a brownish soUd. Mp = 125-126 °C. c) (RS)-l-(4-Benzyloxy-phenyl)-2-oxo-p}TroUdine-3-carbonitrile 300 mg (0.87 mmol) of (RS)-l-(4-benzyloxy-phenyl)-3-bromo-pyrroHdin-2-one is dissolved in 5 ml N,N-dimethylformamide. 64 mg (1.3 mmol) sodium cyanide and 13 mg 0.09 mmol) sodium iodide are added and the suspension stirred for 10 min. at 120 °C. 'he reaction mixture is treated with water and extracted with ethyl acetate to yield 33 mg 13 %) of a colorless solid. MS: m/e = 293.3 (M+ H)"". ixample 2: (RS)-1 -[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid methylamide .) l-(4-Benzyloxy-phenyl)-pyrrolidin-2-one '.03 g (101.9 mmol) 4-benzyloxyaniline and 9.1 ml (119.2 mmol) gamma-butyro-lactone ire treated with 3ml concentrated hydrochloric acid. The mixture is heated 20 hours to .60°C, then 5.5 hours to 200°C. After cooling, the mixture is extracted with 250 ml ethyl icetate, washed with saturated aqueous sodium hydrogencarbonate and dried. Evapora-ion of the solvent and recrystallisation from diethyl ether yields 8.4 g (31 %) of a )rownish solid. MS: m/e = 267 (M"‘). )) l-(4-Hydroxy-phenyl)-pyrrolidin-2-one 5.2 g (23.2 mmol) l-(4-benzyloxy-phenyI)-pyrrolidin-2-one is dissolved in 200 ml THF. 3 irops of acetic acid are added and the solution is hydrogenated for 5 hours at RT and nor-nal pressure in presence of 0.62 g palladium 10 % on charcoal. Filtration and concentra-lion gives a semisolid material. Chromatography (silica gel, dichloromethane / methanol ?5 : 5) yields 2.73 g (66 %) of a brownish soHd. MS: m/e = 175.9 (M-H). z) l-[4-(3-Fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one A. mixture of 2.73 g (15.4 mmol) of l-(4-hydroxy-phenyl)-pyrrolidin-2-one, 3.2 g (16.9 mmol) of 3-fluorobenzylbromide and 4.26 g (31 mmol) of potassium carbonate in 100 ml of 2-butanone is heated at 80°C for 18 hours. After cooling to RT, the reaction mixture is treated with water and ethyl acetate. The organic layer is separated, dried over magnesium sulfate and evaporated under reduced pressure. The solid residue is cr)'stallised from ether to yield 3.86 g (88% of theory) of l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrroHdin-2-one as a colorless solid. MS: m/e = 286.0 (M+ H)’. d) l-[4-(3-Fluoro-benzylox}0-phenyl]-2-oxo-pyrrolidine-3-carboxyHc acid ethyl ester 370 mg (15.4 mmol) sodium hydride is suspended in 20 ml THF and 911 mg (7.7 mmol) diethylcarbonate is added. The suspension is heated to reflux temperature, A solution of 2.0 g (7.0 mmol) l-[4-(3-Fluoro-benzyIoxy)-phenyl]-pyrrolidin-2-one in 10 ml THF is slowly added into the boiling solution. The mixture is boiled for another 5 hours, then hydrolysed with cold water and washed successively with water, saturated sodium hydro¬gencarbonate solution, water and saturated sodium chloride solution. Chromatography (siKca gel, dichloromethane / ethyl acetate) yields 1.3 g (52 %) of a yellowish semisolid. MS: m/e = 358.2 (M+ H)’. s) (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyi]-2-oxo-pyTrolidine-3-carbox)dic acid methyl-amide 300 mg (0.84 mmol) l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid ethyl ester is dissolved in 2 ml N,N-dimethylformamide. 0.17 ml (4.2 mmol) of a 33 % solution of methylamine in ethanol is added. The reaction vessel is tightly stoppered and heated to 120°C for 24 hours. Addition of water precipitates the crude material. Chroma¬tography (silica gel, dichloromethane / methanol) yields 41 mg (14 %) of a yellowish solid. MS: m/e = 343.2 (M+ H)+. Examples: (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide a) l-(3-Fluorobenzyloxy)-4-nitro-benzene A mixture of 5.04 g (40 mmol) 3-fluorobenzyl alcohol and 1.29 g (4mmol) tris-(dioxa-3,6-heptyl)amine is treated with 2.47 g (44 mmol) of potassium hydroxide. The mixture is stirred at RT for 10 min, then 5.55 g (44 mmol) of 4-fluoro-nitrobenzene is slowly added through a dropping funnel. The mixture is kept for 45 min at 80°C, cooled to RT and di¬luted with about 75 ml water. Extraction with ethyl acetate and washing with 2M aqueous hydrochloric acid yields a yellowish organic phase, which is dried and evaporated. The residue is recrystallised from methanol to give 6.07 g (61 %) of the title compound. Yellow crystals, mp = 104-105 °C. b) 4-(3-Fluoro-benzyloxy)-phenylamine 3 g (12.1 mmol) of l-(3-fluorobenzyloxy)-4-nitro-benzene is dissolved in 125 ml of methanol. 150 mg of Pt 5% on charcoal is added and hydrogenation done under normal pressure for about 17 h. The catalyst is filtered and the solution evaporated to yield 2.51 g (95%) of crude brownish material. MS: m/e = 218.4 (M+H)"‘. c) (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrroHdine-3-carbox)dic acid A solution of 561 mg (2.6 mmol) 4-(3-fluoro-benzyloxy)-phenylamine and 448 mg (2.6 mmol) 6,6-dimethyl-5,7-dioxa-spiro[2,5]octane-4,8-dione in 2ml dichloromethane is refluxed for 16 hours. 5 ml of diethylether is added and the precipitate filtered off to yield 485 mg (57 %) of a colorless solid. MS: m/e = 330.2 (M+H)’. d) (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrroHdine-3-carboxylic acid amide 300 mg (0.91 mmol) (RS)-l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrroHdine-3-carb- oxylic acid is dissolved in 2 ml dichloromethane plus 2 drops of N,N-dimethyl-formamide. The solution is cooled to 0 °C and treated with 173 mg (1.37 mmol) oxalyl chloride. After 1 hour at 0 °C the solvent is removed under vacuum at RT. The residue is taken up in 1 ml dichloromethane and slowly added to a mixture of 2 ml THF and 5 ml concentrated ammonia. Stirring is continued for 1 hour at RT. Evaporation of the solvents and dilution with water yields a precipitate, which is filtered off. Recrystallisation fi-om methanol yields 112 mg (37 %) of a colorless soHd. MS: m/e = 329.2 (M+H)’. Example 4: (RS)-l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide a) l-(4-Fluorobenzyloxy)-4-nitro-benzene The title compound is prepared in analogy to Example 3a) from 4-fluorobenzyl alcohol and 4-fluoro-nitrobenzene. Yield : 86 % of a yellowish sohd. Mp = 124-126°C. b) 4-(4-Fluoro-benzyloxy)-phenylamine The title compound is prepared in analogy to Example 3b) by reduction of l-(4-fluoro-benzyloxy)-4-nitro-benzene. Yield: 98 % of a red soHd. MS: m/e = 218.3 (M+H)"‘. c) (RS)-l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylicacid The title compound is prepared in analogy to Example 3c) from 4-(4-fluoro-benzyloxy)-phenylamine and 6,6-dimethyl-5,7-dioxa-spiro[2,5]octane-4,8-dione. Yield : 56 % of a colorless soHd. MS: m/e = 284.1 (M-CO2). d) (RS)-l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxyUc acid amide The title compound is prepared in analogy to Example 3d) from (RS)-l-[4-(4-fIuoro- benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid and ammonia. Yield : 18% of a brownish solid. MS: m/e = 329.3 (M’+ H). Example 5: (RS)-1- [4-(4-Fluoro-benzyloxy)-phenyl] -2-oxo-p-jT:rolidine-3-carboxylic acid mefhylamide The title compound is prepared in analogy to Example 3d) firom (RS)-l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid and methylamine. Yield : 17% of a colorless solid. MS: m/e = 343.2 (M+H)"‘. Example 6: (RS)-2-Oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid amide a) l-(4-Trifluoromethyl-benzyloxy)-4-nitro-benzene The title compound is prepared in analogy to Example 3a) from 4-fluoro-nitro-benzene and 4-trifluoromethyl-benzyl alcohol. Yield 82 % of a shghtly brown sohd. Mp. = 80.5 -81.5 °C. b) 4-(4-Trifluoromethyl-benzyloxy)-phenylamine The title compound is prepared in analogy to Example 3b) by reduction of l-(4-tri-fluoromethyl-benzyloxy)-4-nitro-benzene. Yield : 91 % of a yellowish sohd. MS: m/e = 268.3 (M+H)-". c) (RS)-2-Oxo-l-[4-(4-trifiuoromethyl-benzyloxy)-phenyl]-pyrrohdine-3-carboxylic acid The title compound is prepared in analogy to Example 3c) from 4-(4-trifluoro-methyl-benzyloxy)-phenylamine and 6,6-dimethyl-5,7-dioxa-spiro[2,5]octane-4,8-dione. Yield : 37 % of a colorless soHd. MS: m/e = 380.1 (M+H)’. d) (RS)-2-Oxo-l-[4-(4-trifIuoromethyl-benzyIoxy)-phenyl]-pyrrolidine-3-carboxylicacid amide 150 mg (0.4 mmol) (RS)-2-oxo-l-[4-(4-trifluoromethyI-benzyloxy)-phenyl]-pyrrolidine-3-carboxyhc acid is dissolved in 4 ml THE. 59 mg (0.43 mmol) of 1-hydroxybenzotriazole and 80 mg (0.42 mmol) of N-(3-dimethylaminopropyl)-N'-eth7l-carbodiimide-hydro-chloride is added and the reaction mixture is stirred at RT for 30 min. After cooling to 0°C 4ml of concentrated ammonia is added and the resulting mixture stirred at RT for 1 hour. Dilution with water, extraction and chromatography (silica gel, ethyl acetate) yields 15 mg (10 %) of a colorless solid. MS: m/e = 379.2 (M+H)"". Example 7: (RS)-2-Oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid methylamide The title compound is prepared in analogy to Example 6d) from (RS)-2-oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carbox7lic acid and methylamine. Yield: 6 % of a colorless solid. MS: m/e = 393.2 (M+H)’. Examples: (S)-N-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-acetamide a) (S)-[l-(4-Benzyloxy-phenylcarbamoyl)-3-methylsulfanyl-propyl]-carbamic acid tert-but)'l ester A solution of 0.57 g (2.3 mmol) of (S)-Boc-methionine in 5 ml of dichloromethane is treated at RT consecutively with 0.87 g (2.3 mmol) of 0-(benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium-hexafluorophosphate (HBTU), 0.50 g (2.1 mmol) of 4-benzyloxy-aniline hydrochloride and 0.98 ml (5.7 mmol) of N-ethyl-diisopropylamine. The reaction mixture is stirred during 1 h at RT. For the working-up, the reaction mixture is diluted with dichloromethane and treated with 20 ml of an aqueous solution of citric acid (10%). The aqueous phase is re-extracted with dichloromethane, the organic phases combined, dried over sodium sulfate and evaporated under reduced pressure. For purification, the crude material obtained is chromatographed on silica gel using a 3:1 mixture of n-hexane and etiiyl acetate as the eluent There are obtained 0.74 g (82.5% of theory) of (S)-[l-(4- benzyioxy-phenylcarbamoyl)-3-methylsulfanyl-propyl]-carbamic acid tert-but)’l ester as a white soHd. MS: m/e = 431 (M+H)’ b) (S)-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidiii-3-yl]-carbamic acid tert-butyl ester A mixture of 0.35 g (0.81 mmol) of (S)-[l-(4-benzyloxy-phenylcarbamoyl)-3-methyl-sulfanyl-p’opyl]-carbamic acid tert-butyl ester and 8.79 g (62.0 mmol) of methyHodide is stirred at.RT for 3 d. Thereafter, the methyliodide is evaporated, the intermediate sulf-onium salt dissolved in 15 ml of THF and treated with 0.79 ml (0.79 ml) of lithium bis-(trimethylsilyl) amide (1 M solution in THF) at 0°C. After stirring at 0°C for 2 h, the reaction mixture is evaporated under reduced pressure and the solid residue is directly submitted to chromatography on silica gel using a 2:1 mixture of n-hexane and ethyl acetate as the eluent. There are obtained 0.175 mg (56% of theory) of (S)-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester as a white solid. MS: m/e = 383 (M+H)’ c) (S)-3-Amino-l-(4-benzyloxy-phenyl)-pyrrolidin-2-one hydrochloride A solution of 137 mg (0.36 mmol) of (S)-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester in 2 ml of dioxane is treated with 0.3 ml of hydrochloric acid (37%). The solution is warmed to 45°C for 1 h forming a white suspension. For the worlc-ing-up, the reaction mixture is evaporated under reduced pressure and the solid residue is triturated with a small volume of methanol. After filtration and drying, 94 mg of (S)-3-amino-l-(4-benzyloxy-phenyl)-p"5Trolidin-2-one hydrochloride (82% of theory) are ob¬tained as a white solid. MS: m/e = 283 (M + H)"‘. d) (S)-N-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrohdin-3-yl]-acetamide A solution of 40 mg (0.13 mmol) of (S)-3-amino-l-(4-benzyloxy-phenyl)-pyrrolidin-2-one hydrochloride in 2 ml of dichloromethane is treated with 38 p.1 (0.28 mmol) of tri-ethylamine and cooled to 0°C. To this solution, 10 [il (0.14 mmol) of acetylchloride are added and stirring at 0°C is continued for 30 min. For the working-up, the reaction mix¬ture is treated with 2 ml of ammonium hydroxide solution, the organic phase separated, thereafter dried over sodium sulfate and evaporated under reduced pressure. For purifi¬cation, the material obtained is chromatographed on silica gel using a 95:5 mixture of di¬chloromethane and methanol as the eluent. There are obtained 31 mg (76% of theory) of (S)-N-[l-(4-enzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-acetamide as a white solid. MS: m/e = 325 (M+H)"-. Example 9: (S)-N-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-methanesulfGn-amide In an anologous manner to that described in Example 8d), the reaction of (S)-3-amino-l-(4-benzyloxy-phenyl)-pyrrohdin-2-one hydrochloride with methanesulfochloride in the presence of triethylamine yields (S)-N-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-methanesulfonamide as a white soUd. MS: m/e = 361 (M+H)"". Example 10: (S)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide a) In an anologous manner to that described in Example 8a) to c), the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride is obtained: Condensation of (S)-BOC-methionine and 4-(3-fluorobenzyloxy)-phenylamine [Example 3b)] by HBTU yields the (S)-{l-[4-(3-fluoro-benzyloxy)-phenylcarbamoyl]-3-methylsulfanyl-propyl}-carbamic acid tert-butyl ester as a light yellow solid; MS: m/e = 449 (M+H)"‘. The following methylation and cyclisation yields the (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert-butyl ester as a white solid; MS: m/e = 401 (M+H)"‘. The cleavage of the BOC-group yields the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrohdin-2-one hydrochloride as a white solid; MS: m/e = 301 (M+H)"". b)lS)-N-{l-[4-(3-fluoro-benzylox}')-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide In an anologous manner to that described in Example 8d), the acetylation of the (S)-3-amino-l-[4-(3-fludro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 343 (M-l-H)"‘. Example II: (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide, (R)-N"{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-p}T:rolidin-3-yl}-methanesulfonamide, (S)-N-{1 - [4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-methanesulfonamide and (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid methyl ester In an anologous manner to that described in Example 8 d), the acylation of (R)- or (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride [the (R)-isomer is obtained in analogy to the (S)-isomer as described in Example 10 a) starting from (R)-BOC-methionine] yield the following compounds: ) Reaction of the (R)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one ydrochloride with acetylchloride yields the (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2- xo-pyrrolidin-3-yl}-acetamide as a white soHd; MS: m/e = 343 (M+H)"‘. ') Reaction of the (R)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one lydrochloride with methanesulfochloride yields the (R)-N-{l-[4-(3-fluoro-benzyloxy)- ihenyl]-2-oxo-pyrrolidin-3-yl}-methanesulfonamide as a white solid; MS: m/e = 377 M-hH)"'. :) Reaction of the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one lydrochloride with methanesulfochloride yields the (S)-N-{l-[4-(3-fluoro-benzyloxy)- )henyl]-2-oxo-pyrrohdin-3-yl}-methanesulfonamide as a white solid; MS: m/e = 377 M+Hf. i) Reaction of the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one lydrochloride with methyl chloroformate yields the (S)-{l-[4-(3-fluoro-benzyloxy)- 3henyl]-2-oxo-p}Trolidin-3-yl}-carbamic acid methyl ester as a white solid; MS: m/e = 359 :M+H)"'. Example 12: (R)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yI}-formamide A. mixture of 188 mg (18 mmol) of acetic anhydride and 107 mg (23 mmol) of formic acid is prepared at 0°C, thereafter, heated to 60°C for 2 hours.After cooHng to RT, the mixture is diluted with 1 ml of tetrahydrofiirane and a solution of 213 mg (7 mmol) of (R)-3-amino-l-[4-(3-fiuoro-benzyloxy)-phenyl]-pyrrolidin-2-one in 2 ml of dichloromethane, beforehand prepared from the corresponding hydrochloride by treatment with triethylamine, is added. After the addition a white suspension is formed which is stirred at RT for 1 hour. For the working-up, the reaction mixture is treated with dichloromethane and water, then, the organic layer is separated, dried over sodium sulfate and evaporated. There are obtained 215 mg (92% of theory) of (R)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyTrolidin-3-yl}-formamide as a white soHd; MS: m/e = 329 (M+H) . Example 13: (S)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-formamide In an analogous manner to that described in Example 12, the reaction of (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one with a mixture of acetic anhydride and formic acid yields the title compound as a white soHd; MS: mZe = 329 (M+H) . Example 14: (R)-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrroUdin-3-yl}-urea A solution of 250 mg (0.7 mmol) of (R)-3-amino-l-[4-(3-fluoro-benzyIoxy)-phenyl]-pyrrolidin-2-one hydrochloride and 294 mg (2.2 mmol) of N-ethyl-diisopropylamine in 2 ml of N,N-diinethylformamide is cooled to 0°C and treated with 267 mg (2.2 mol) of trimethylisocyanate. The reaction mixture is left to warm to RT and stirring is continued for 2 days. For the working-up, the suspension is evaporated under reduced pressure. The crude product is triturated in water, then the recovered solid material triturated a second time in a mixture of ethyl acetate and a saturated solution of sodium hydrogencarbonate. The remaining solid is collected on a filter funnel to give, after drying under high vacuum, 155 mg (61% of theory) of (R)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-urea as a white solid; MS: m/e = 344 (M+H)"‘. Example 15: (S)-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidLn-3-yl}-urea In an analogous manner to that described in Example 14, the reaction of (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one trimethylisocyanate yields the title compound as a white solid; MS: m/e = 344 (M+H)"". Example 16: (S)-N-{l-(S)-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide a) (S)-[l-(4-Hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester In an analogous manner to that described in Example 2b), the hydrogenolysis of the.(S)-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester [Example 8 b)] using palladium on carbon as the catalyst yields the title compound as a white solid in quantitative yield; MS: m/e= 291 (M-H)"‘. b) (S)-{l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert- butyl ester In an analogous manner to that described in Example 2c), the alkylation of the (S)-[l-(4-hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester with 4-fluorobenzylbromide in presence of potassium carbonate yields the title compound as a white solid; MS: m/e= 401 (M+H)’. c) (S)-3-Amino-l-[4-(4-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride In an analogous manner to that described in Example 8c), the cleavage of the BOC-group of the (S)-{l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-carbamic acid tert-butyl ester yields the title compound as a white sohd; MS: m/e= 301 (M-f-H) . d) (S)-N-{l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide In an anologous manner to that described in Example 8 d), the acetylation of the (S)-3-amino-l-[4-(4-fluoro-benzyIoxy)-phenyl]-p}arohdin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 343 (M+H)"‘. Example 17: (S)-N-{l-(S)-[4-(2,6-Difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yI}-acetamide a) (S)-{l-[4-(2,6-Difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert- butyl ester In an analogous manner to that described in Example 2c), the alkylation of the (S)-[l-(4-hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acidtert-butyl ester [Example 16 a)] with 2,6-difluorobenzylbromide in presence of potassium carbonate yields the title compound as a white solid; MS: m/e= 419 (M+H)"‘. b) (S)-3-Amino-l-[4-(2,6-difluoro-benzylox}')-phenyl]-pyrrolidin-2-one hydrochloride In an analogous manner to that described in Example 8c), the cleavage of the BOC-group of the (S)-{l-[4-(2,6-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert-butyl ester yields the title compound as a white solid. c) (S)-N-{l-[4-(2,6-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide In an anologous manner to that described in Example 8 d), the acetylation of the (S)-3-amino-l-[4-(2,6-difluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 361 (M+H)'‘. Example 18: (S)-N-{l-[4-(3,4-Difluoro-benzylox)'-)-phenyl]-2-oxo-pyrroHdiii-3-yl}-acetamide a) (S)-{l-[4-(3,4 -Difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acidtert- butyl ester In an analogous manner to that described in Example 2c), the alkylation of the (S)-[l-(4-hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acidtert-butyl ester [Example 16 a)] with 3,4-difluorobenzylbroniide in presence of potassium carbonate yields the title compound as a white solid; MS: m/e= 419 (M+H)"". b) (S)-3-Amino-l-[4-(3,4-difluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride In an analogous manner to that described in Example 8c), the cleavage of the BOC-group of the (S)-{l-[4-(3,4-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamicacid tert-butyl ester yields the title compound as a white solid; MS : m/e= 319 (M+H)"". c) (S)-N-{l-[4-(3,4-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-acetamide In an anologous manner to that described in Example 8 d), the acet}'lation of the (S)-3-amino-l-[4-(3,4-difluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 361 (M+H)''. Example A: Tablets Tablets of the following composition are produced in a conventional manner: mg/Tablet Active ingredient 100 Powdered lactose 95 White corn starch 35 Polyvinylpyrrolidone 8 Na carboxymethylstarch 10 Magnesium stearate 2 Tablet weight 250 Example B: Tablets Tablets of the following composition are produced in a conventional manner: mg/Tablet Active ingredient 200 Powdered lactose 100 White corn starch 64 Polyvinylpyrrolidone 12 Na carboxymethylstarch 20 Magnesium stearate 4 Tablet weight 400 Example C: Capsules Capsules of the following composition are produced: mg/Capsule Active ingredient 50 Crystalline lactose 60 Microcrystalline cellulose 34 Talc 5 Magnesium stearate 1 Capsule fill weight 150 The active ingredient having a suitable particle size, the crystalline lactose and the micro-crystalline cellulose are homogeneously mixed with one another, sieved and thereafter talc and magnesium stearate are admixed. The final mixture is filled into hard gelatine capsules of suitable size. Example D: Injection solution An injection solution may have the following composition and is manufactured in usual manner: Active substance 1.0 mg 1 N HCl 20.0 III acetic acid 0.5 mg NaCl 8.0 mg phenol 10.0 mg INNaOH q.s. adpH5 H2O q.s. ad 1 ml WE CLAIM: 1, A pompom of the formula I wherein X-Yis -CH2-CH2-, -CH=CH- or ;Hj-O-; R', R;' and R ; independently from each other are selected from the group consisting of hydrogen, halogen, cyan, (CrC6)-aIkyl, halogen-(Ci-C6)-alkyl, (Ic-Q)-alkoxy or halogen- (Ic-Qs)-alkoxy; R;\ R; and R; independently from each other are selected from the group consisting of hydrogen and halogen; R;* is hydrogen, halogen or methyl R' is hydrogen; R* is-CONHR;-Nor-NHR; R is hydrogen or (CrC3)-aIkyl; and R' is -CO-H, -CO'(Ic-Q)-alkyl, .CO-halogen-(CrC3)-a]k)d, -C0-0-(Ci-C3)-aIkyl, -CO-NH2 or -S02-(Ci-C5)-alkyl; as well as individual isomers, racemic or non-racemic mixtures thereof. 2.The compound as claimed in claim-1, wherein X-Y is -CH2-CH2-. 3. The compound as claimed in claim 1 ,wherein R; R"; and R;; independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmeth';, cyan, methoxy or halogen-methoxy. 4. The compound as claimed in claim 1, wherein R;S R;; and R; are hydrogen. 5. The compound as claimed in claim 1, wherein R** is hydrogen. 6. The compound as claimed in claim 1, wherein R* is -CONHR', wherein R; is hydrogen or (Ci-C3)-alkyd. 7. The compound as claimed in claim 1 ,wherein R* is -CN. 8. The compound as claimed in claim 1, wherein R* is -NHR; herein R; is -CO-H, -CO-(Ci-C6)-alkyl, -CO-halogen-(Ci-Ca)-alky], -CO-0-{Ci-Cs)- -CO-NH2 or -S02-(C,-Q)-alkyd. 9. The compound as claimed in claim 1, wherein the compound has (S)-configuration 10. The compound as claimed in claim wherein the compound has (R)-configuration. 11. The compound as claimed in claim wherein the compound is selected from (RS)-l-(4-ben2yio3cy-phenyi)'2-oxo-pyrrolidine-3-carbonitrile, (RS)-l- [4-(3-fluoro-bciizyloxy)-phenyl] -2-oxo-pyrrolidiQe-3-carboxylic add methylamide, (RS)-l-[4-(3-fluoro-ben27loxy)-phenyi]-2-oxo-pyrrolidine-3-carboacyiic acid amide, (RS)-l-[4-(4-fluoro-benzyioxy)-phenyl]-2-os:o-pyrrolidine-3-carbo3jyIic acid amide, (RS)-l-(4-(4-fluoro-benzyloxy)-phenyl] -2-oxo-pyrrolidine-3-carboxylic acid methylamide, (RS)-2-oxo-l-[4-(4-trifluoromethyl-benzylo3cy)-phenyI]-pyrroIidine-3-carboxyUc add amide, (RS)-2-oxo-l-[4-(4-tri£luoromethyI-benzyloxy)-phenyl]-pyrrolidine-3-carboryiicadd methylamide, (S)-N-[l-(4-ben2yloxy-phenyi)'2-oxo-pyrroIidin-3-yl]-acetamide, (S)-N-11 - (4'benzyioxy-phenyI)-2-oxo-pyirolidin-3-yI] -mcthanesxilfonamidc, (S)-N-{ 1 - [4-(3-auoro-b enzjdoxy)-phen3d] -2-oxo-pyrrclidin-3 -;}-acetamide, (R)-N-{l-[4-(3-fluoro-ben2yioxy)-phenylI-2-oxo-pyrrolidin-3-yI}-acetamide, (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yi}-methanesulfonaniide, (S)-N-{ 1 - [4-(3-fiuoro-benzyiQxy)-phenyl] -2-oxo-pyrrolidin-3-yi}-methanesuIfonamide, (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yi}-caibamic acid methyl ester, (R) -N-{ 1 - [4-(3-fluoro-benzyloxy) -phenyl) -2-oxo-pyrrolidin-3-yl} -formamide, (S)-N-{l-[4-(3-fluoro-ben2yioxy)-phen54]-2-oxo-pyrrolidin-3-yl}-formative, (R)-{l-[4-(3-fluoro-ben2yioxy)-phenyI]-2-oxo-pyrroIidin-3-yI}-urea, (S)-{l-[4-(3-fluoro-benzyloxy)-phenylI-2-oxo-pyxTolidin-3-yl}-U)rea, (S)-N-{l-(S)-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide, (S)-N-{ l'(S)- [4-(2,6-difluoro-ben2yloxy)-phenyl]-2-oxo-pytrQlidin-3-yI}-acetamide and (S)-N-{l-[4-(3,4-difluoro-benzjioxy)-phen'yI]-2-oxo-pyrroIidin-3-)4}-acetamide. 12. A process for the preparation of compounds of formula I as claimed in claim wherein (a)RisCONHR comprising reacting a compound of formula II (H) wherein R\ R;-\ R'•; r', R;, R», R», R>, X and Y have the meanings as defined above and R is hydrogen, with thionyl chloride or oxalyl chloride, or with DCC or EDC, and subsequent coupling with an amine of formula H2N-R; wherein R* has the meaning.as defined in daim 1; (b)RisCN comprising reacting a compound of formula III (HI) wherein R; R; R;-;, R", R;, R;, R", R', X and Y have the meanings as defined above and Hal is halogen, with sodium or potassium cyanide in N,N-dimethylformamide, acetone or acetonitrile at a temperature in the range of from 20°C to 140°C, and optional catalytic amounts of sodium or potassium iodide; or (c)RisNHR comprising reacting a compound of formula IV R'; x.;iA,.o (IV) wherein R\ R;"\ R;■; R", R;, R;, R", R', X and Y have the meanings a$ defined above, with an acyl donating agent of formula Z-CO-H, Z-CO-(Ci-C6)-alkyl, Z-CO-halogen-CCi-Cj)-alkyi, Z-CO-0-(Ci-C3)-alkyi, or Z-S02-(Ci-C3)-a]kyl wherein Z is an activating group, eg. a halogen or anhydride, or with an isocyanate. 13. The compound of the formula I* as claimed in claim 1, Wherein R' is halogen, halogen-(Ci-C6)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(Ci-C6)-alkoxy; R , R , R and R independently from each other are selected from the group consisting of hydrogen and halogen; R' is hydrogen; R; is-CONHR; -CH2CN-CN or-NHR; R; is hydrogen or CpCs-alkyl; R; is C0-(CrC6)-alkyl or-S02-(Ci-C6)-alkyl; and N is 0, 1, 2 or 3; as well as individual isomers, racemic or non-racemic mixtures thereof 14. A pharmaceutical composition containing a compound as claimed in claim 1 or 13, and pharmaceutically acceptable excipients.

Full Text

The invention relates to 4-pyrrolidino -phenyl-benzyl ether derivatives- In particular racemes or enantiomerically pure 4-pyrrolidino derivatives, processes for
their preparation, pharmaceutical compositions comprising said derivatives, and their use in the prevention and treatment of illness.
More particularly, the present invention relates to compounds of the formula I

R" , R"', R"" and R independently from each other are selected from the group consisting
of hydrogen and halogen; R is hydrogen;
R’ is-CONHR’-CH2CN,-CNo’-NHR’; R is hydrogen or Ci-Cs-alkyI; R’ is-C0-(Ci-C6)-alkyl or-S02-(Ci-C6)-alkyl; and n is 0,1,2 or 3; as well as individual isomers, racemic or non-racemic mixtures thereof.
It has been found that the compounds of general formula I and P as well as individual isomers, racemic or non-racemic mixtures thereof (hereinafter: Active Compounds) are selective monoamine oxidase B inhibitors.
Monoamine oxidase (MAO, EC 1.4.3.4) is a flaking-containing enzyme responsible for the oxidative deamination of endogenouslnonoamine neurotransmitters such as dopamine, serotonin, adrenaline, or noradrenaline, and trace amines, e.g. phenylethyl-amine, as wet as a number of amine xenobiotics. The enzyme exists in two forms, MAO-A and A'lAO-B, encoded by different genes [Bach et al, Proc. Natl. Acad. Sci. USA 85:4934-4938 (1988)] and differing in tissue distribution, structure and substrate specificity. MAO-A has higher affinity for serotonin, octopamine, adrenaline, and noradrenaline; whereas the natural substrates for MAO-B are phenylethylamine and t’'ramine. Dopamine is thought to be oxidised by both isoforms. MAO-B is widely distributed in several organs including brain [Cesura and Pletscher, Prog. Drug Research 38:171-297 (1992)]. Brain MAO-B activity appears to increase with age. This increase has been attributed to the gliosis associated with aging [Fowler et al., J. Neural. Transm. 49:1-20 (1980)]. Additionally, MAO-B activity is significantly higher in the brains of patients with Alzheimer's disease [Dostert et al, Bio-chem. Pharmacol. 38:555-561 (1989)] and it has been found to be highly expressed in astrocytes around senile plaques [Saura et al., Neuroscience 70:755-774 (1994)]. In this context, since oxidative deamination of primary monoamines by MAO produces NH3, aldehydes and H2O2, agents with established or potential toxicity, it is suggested that there is a rationale for the use of selective MAO-B inhibitors for the treatment of dementia and Parkinson's disease. Inhibition of MAO-B causes a reduction in the enzymatic inactivation of dopamine and thus prolongation of the availability of the neurotransmitter in dopa¬minergic neurons. The degeneration processes associated with age and Alzheimer's and Parkinson's diseases may also be attributed to oxidative stress due to increased MAO acti¬vity and consequent increased formation of H2O2 by MAO-B. Therefore, MAO-B inhibi-

tors may act by both reducing the formation of oxygen radicals and elevating the levels of monoamines in the brain.
Given the implication of MAO-B in the neurological disorders mentioned above, there is considerable interest to obtain potent and selective inhibitors that would permit control over this enzymatic activity. The pharmacology of some known MAO-B inhibitors is for example discussed by Bentue-Ferrer et al. [CNS Drugs 6:217-236 (1996)]. Whereas a major limitation of irreversible and non-selective MAO inhibitor activity isthe need to observe dietary precautions due to the risk of inducing a hypertensive crisis when dietary tyramine is ingested, as well as the potential for interactions with other medications [Gardner et al., J. Clin. Psychiatry 57:99-104 (1996)], these adverse events are of less concern with rever¬sible and selective MAO inhibitors, in particular of MAO-B. Thus, there is a need for MAO-B inhibitors with a high selectivity and without the adverse side-effects typical of irreversible MAO inhibitors with low selectivity for the en2yme.
The following definitions of general terms used herein apply irrespective of whether the terms in question appear alone or in combination. It must be noted that, as used in the specification and the appended claims, the singular forms "a", "an," and "the" include plural forms unless the context clearly dictates otherwise.
The term "(Ci-C6)-alkyr' used in the present application denotes straight-chain or branched saturated hydrocarbon residues with 1 to 6 carbon atoms, such as methyl, ethyl, n-propyl, i-propyl, n-butyl, sec-butyl, t-butyl, and the like, preferably with 1 to 3 carbon atoms. Accordingly, the term "(Ci-C3)-aIkyr' means a straight-chain or branched saturated hydrocarbon residue with 1 to 3 carbon atoms.
The term "halogen" denotes fluorine, chlorine, bromine and iodine.
"Halogen-(Ci-C6)-alkyr or "halogen-(CrC6)-alkoxy" means the lower alkyl residue or lower alkoxy residue, respectively, as defined herein substituted in any position with one or more halogen atoms as defined herein. Examples of halogenalkyl residues include, but are not limited to, 1,2-difluoropropyl, 1,2-dichloropropyl, trifluoromethyl, 2,2,2-trifluoro-ethyl, 2,2,2-trichloroethyl, and 3,3,3-trifluoropropyl,~and the like. "Halogenalkoxy" in¬cludes trifluoromethyloxy.
"(Ci-C6)-AIkoxy" means the residue -O-R, wherein R is a lower alkyl residue as defined herein. Examples of alkoxy radicals include, but are not limited to, methoxy, ethoxy, iso- ■ propoxy, and the like.

"Pharmaceutically acceptable salts" of a compound means salts that are pharmaceutically acceptable, which are generally safe, non-toxic, and neither biologically nor otherwise un¬desirable, and that possess the desired pharmacological activity of the parent compound. These salts are derived from dn inorganic or organic acid or base. If possible, compounds of formula I maybe converted into pharmaceutically acceptable salts. It should be understood that pharmaceutically acceptable salts are included in the present invention.
In another embodiment the present invention provides compounds of formula F, wherein R’ is hydrogen and R* is selected from the group consisting of-CONHR’, -CH2CN, or -CN.
Those compounds of formula I*, wherein R* is -CONHR’ and R’ is hydrogen or (C1-C3)-
alkyl, are especially preferred. Examples of such compounds are
(RS)-l-[4-(3-fluoro-benzyloxy)-phenyl] -2-oxO-pyrrolidine-3-carboxylic acid
methylamide;
(RS)-l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide;
(RS)-l-[4-(4-fluoro-ben2yloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxyhc acid amide;
(RS)-l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylicacid
methylamide;
(RS)-2-oxo-l-[4-(4-tri£luoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxyHcacid
amide; and
(RS)-2-oxo-1 -[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxyhc acid
methylamide.
Another group of preferred compounds of formula P are those, wherein R* is -CN. (RS)--l-(4-benzylox}’-phenyl)-2-oxo-pyrrolidine-3-carbonitrile is an example of such a compound.
Also preferred are compounds of formula F, wherein R’ is hydrogen, R is -NHR and R is -C0-(Ci-C6)-alkyl or -S02-(Ci-C6)-alkyl. Examples of such compounds are (S)-N-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrohdin-3-yl]-acetamideand(S)-N-[l-(4-benzylox)’-phenyl)-2-oxo-pyrrolidin-3-yl]-methanesulfonamide.
Compounds of formula F maybe substituted by n R’ selected from the group consisting of halogen, halogen-(CrC6)-alkyl, cyano, (Ci-C6)-aIkoxy or halogen-(Ci-C6)-alkoxy, wherein n denotes an integer selected from 0, 1, 2 and 3. Preferably n is 1 or 2. Preferred compounds of formula F are those, wherein R’ is halogen or halogen-(Ci-C6)-alkyl. Especially preferred are those compounds of formula F, wherein R is fluorine, chlorine or

trifluoromethyl. W’ere the compounds of formula P are substituted by two or three R\ each R can be the same or different.
In one embodiment the invention provides compounds of formula I wherein -X-Y- is -CH2-O-. In another embodiment the invention provides compounds of formula I where¬in -X-Y- is -CH2-CH2- or -CH=CH-.
In one embodiment the invention provides compounds of formutla I wherein R’ R’'‘ and R ■ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, cyano, methoxy or halogen-methoxy. In another embodi¬ment the present invention provides compounds of formula I wherein R\ R'"' and R’'‘ are halogen, e.g. fluoro, e.g. 2,4,6-trifluoro, 2,4,5-trifluoro, 2,3,6-trifluoro, 2,3,4-trifluoro or 3,4,5-trifluoro. In still another embodiment the present invention provides compounds of formula I wherein R'"'‘ is hydrogen and R’ and R’' independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-C6)-allcyl,' halogen-(Ci-Q)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(CrC6)-alkoxy. In still another embodiment the present invention provides compounds of formula I wherein R’'‘ is hydrogen and R’ and R’'‘ independently from each other are selected from the group consisting of halogen and (Ci-C6)-alkyl. In stiU another embodiment the present invention provides compounds of formula I wherein R’'‘ is hydrogen, R’'‘ is halogen and R’ is halogen or (Ci-C6)-alkyl. In still another embodiment the present invention provides compounds of formula I wherein R’'‘ and R’'‘ are hydrogen and R’ is halogen, (Ci-C6)-alkyl, halogen-(Ci-C6)-alkyl, cyano, (Ci-C6)-aIkoxy or halogen-(Ci-C6)-aIkoxy. In still another embodiment the present inven¬tion provides compounds of formula I wherein R’'‘ and R’'‘ are hydrogen and R is halo¬gen, methyl, halogenmethyl, cyano, methoxy or halogen-methoxy. In still another embodi¬ment the present invention provides compounds of formula I wherein R ' and R ■' are hydrogen and R’ is fluoro, e.g. 3-fluoro or 4-fluoro, chloro, e.g. 3-chloro, halogenmethyl, e.g. 3-trifluoromethyl or 4-trifluoromethyl, cyano, methoxy, e.g. 2-methoxy, 3-methoxy or 4-methoxy, or halogen-methoxy, e.g. 3-trifluoromethoxy. In another embodiment the present invention provides compounds of formula I wherein R , R ' and R " are hydrogen.
In one embodiment the present invention provides compounds of formula I wherein R , R’’andR’’ are hydrogen.
In one embodiment the present invention provides compounds of formula I wherein R' is hydrogen.

In one embodiment the present invention provides compounds of formula I wherein R* is -CONHR , wherein R’ is hydrogen or (Ci-C3)-allcyl. In another embodiment the present invention provides compounds of formula I wherein R’ is -CONHR’, wherein R’ is hydrogen or methyl.
In one embodiment the present invention provides compounds of formula I wherein R* is -CN.
In one embodiment the present invention provides compounds of formula I wherein R is -NHR’ wherein R’ is -CO-H, -CO-(Ci-C6)-alkyl, -CO-halogen-(Ci-C3)-alkyl, -CO-O-(CrC3)-allcyl, -CO-NH2 or -S02-(Ci-C6)-alkyl. In another embodiment the present invention provides compounds of formula I wherein R’ is -NHR’, wherein R is -CO-H, -C0-(CrC6)-alkyl, -C0-0-(Ci-C3)-alk)'-l, -CO-NH2 or -S02-(Ci-C6)-alk)d. In still another embodiment the present invention provides compounds of formula I wherein R is -NHR’ wherein R’ is -CO-H, -CO-methyl, -CO-O-methyl, -CO-NHo or -SOz-methyl.
In one aspect the present invention provides compounds of formula I wherein the compounds have (S)-configuration. In one aspect the present invention provides compounds of formula I wherein the compounds have (R)-configuration.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’ R’'‘ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, cyano, methoxy or halogen-methoxy; R’’ R’’ and R’’ are hydrogen; R’" is hydrogen and R’ is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-alkyl.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’'‘ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, q'‘ano, methoxy or halogen-methoxy; R , R " and R are hydrogen; R is hydrogen and R is -CN.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’"‘ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmethyl, cyano, methoxy or halogen-methox}'; R , R"" and R are hydrogen; R is hydrogen and R is -NHR , wherein R is -C0-H,-C0-(Ci-C6)-alkyl, -CO-halogen-(Ci-C3)-alkyl, -C0-0-(Ci-C3)-alkyl, -CO-NH2 or -S02-(Ci-C6)-alkyl.

In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-’ is hydrogen and R’ and R’"‘ independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-CoO-alkyl, halogen-(Ci-C6)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(Ci-C6)-alkoxy; R’’ R’’ and R’’ are hydrogen; R"" is hydrogen; and R* is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-aIkyl.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’' and R’'‘ are hydrogen and R’ is halogen, (Ci-C6)-alkyl, halogen-CCi-Ce)-alkyl, cyano, (Ci-C6)-alkox7 or halogen-(Ci-C6)-alkoxy; R’\ R’" and R’’ are hydrogen; R’’ is hydrogen; and R' is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-allcyl.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’-’ and R’"‘ are hydrogen; R’\ R’’ and R’’ are hydrogen; R’’ is hydrogen; and R’ is -CONHR’ wherein R’ is hydrogen or (Ci-C3)-alkyL
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R '‘ is hydrogen and R and R ' independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-C6)-aIkyl, halogen-(Ci-C6)-aIkyl, cyano, (Gi-C6)-allcoxy or halogen-(Ci-C6)-aIkoxy; R'‘‘ R’’ and R’’ are hydrogen; R’* is hydrogen; and R* is -CN.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’"‘ and R’-’ are hydrogen and R' is halogen, (Ci-C6)-alkyl, halogen-CCi-Ce)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(Ci-C6)-alkoxy; R’\ R’’ and R"‘ are hydrogen; R’* is hydrogen; and R’ is -CN.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R', R’-’ and R’'‘ are hydrogen; R’’ R’’ and R’-' are hydrogen; R'‘ is hydrogen; andR*is-CN.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’'‘ is hydrogen and R’ and R’'‘ independently from each other are selected from the group consisting of hydrogen, halogen, (Ci-C6)-alkyl, halogen-(Ci-C6)-aIkyl, cyano, (Ci-C6)-alkox7 or halogen-(CrC6)-alkoxy; R'‘ R’" and R’"‘ are hydrogen; R’'‘ is hydrogen; and R* is -NHR’ wherein R’ is -CO-H, -C0-(Ci-C6)-alkyl, -CO-halogen-(Ci-C3)-alkTl, -C0-0-(Ci-C3)-alkyl, -CO-NH2 or -S02-(Ci-C6)-alkyl.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-’ andR’-' are hydrogen and R’ is halogen, (Ci-C6)-aIkyl, halogen-(Ci-Ce)-

allcyi, cyano, (Ci-Cgj-alkoxy or halogen-(CrC6)-alkoxy; R’\ R~’ and R'‘ are hydrogen; R’' is hydrogen; and R* is -NHR’ wherein R’ is -CO-H, -C0-(Ci-C6)-alkyl, -CO-halogen-(CrC3)-alkyl, -C0-O-(CrC3)-alkyl, -CO-NH2 or -S02-(Ci-C6)-alkyl.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R\ R’-' and R’-’ are hydrogen; B}\ R’’ and R’’ are hydrogen; R’’ is hydrogen; and R’ is -NHR’ wherein R’ is -CO-H, -C0-(Ci-C6)-aIkyI, -CO-halogen-CCi-QO-alkyI, -C0-0-(Ci-C3)-allcyl, -CO-NH2 or -S02-(CrC6)-alkyl.
In one embodiment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-' and R’'‘ are hydrogen and R’ is halogen; R’\ R’’ and R’’ are hydrogen; R-'‘ is hydrogen; and R* is -NHR’ wherein R’ is -C0-(Ci-C6)-alkyl. In another embodi¬ment the present invention provides compounds of formula I wherein X-Y is -CH2-O-; R’-\ R'-’ R’\ R’\ R-’ and R’’ are hydrogen; R’ is halogen; and R’ is -NHR’ wherein R’ is -CO-methyl.
Examples of compounds of formula I include compounds selected from (RS)-l-(4-benzyloxy-phenyl)-2-oxo-p)Trrolidine-3-carbonitrile, (RS)-l-[4-(3-fluoro-henzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid methyl-amide, (RS)-l-[4-(3-f[uoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide, (RS)-l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxyhc acid amide, (RS)-l-[4-(4-fluoro-ben2yloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid methyl-amide, (RS)-2-oxo-l- [4-(4-trifluoromethyl-benzyloxy)-phenyl] -pyrrohdine-3-carboxylic acid
amide, (RS)-2-oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrroHdine-3-carboxyhcacid
methylamide, (S)-N-[l-(4-benzylox7-phenyl)-2-oxo-pyrroHdin-3-yl]-acetamide, (S)-N-[l-(4-benzyloxy-phenyl)-2-oxo-pyrroHdin-3-yl]-methanesulfonamide, (S)-N-{l-[4-(3-fluoro-benzylox7)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide, (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide, (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-methanesulfonamide, (S)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-methanesulfonamide, (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid methyl
ester,
(R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-formamide, (S)-N-{ 1-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-formamide,

(R)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-urea,
(S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-urea,
(S)-N-{ 1-(S)- [4-(4-fluoro-benzyloxy)-phenyl] -2-oxo-pyrroIidin-3-yl}-acetamide,
(S)-N-{l-(S)-[4-(2,6-difiuoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-acetamideand
(S)-N-{ 1-[4-(3,4-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide.
In one embodiment the present invention provides a process for the preparation of
compounds of formula I wherein
(a)RSsCONHR’
comprising reacting a compound of formula II

(11)

wherein R\ R’\ R’'‘ R’\ R’\ R’’ R’’ R’ X and Y have the meanings as defined above
and R'*' is hydrogen or (Ci-C6)-alkyl,
with an amine of formula H2N-R’, wherein R’ has the above meaning;
(b) R* is CN
comprising reacting a compound of formula III

(HI)

wherein R\ R’-\ R’•’ R’\ R’\ R"‘ R’’ R’ X and Y have the meanings as defined above
and Hal is halogen,
with a cyanide salt; or
(c) R* is NHR’
comprising reacting a compound of formula IV
R=

23 , (

(IV)

wherein R\ R’-\ R’-\ R-\ R’\ R-\ R-’ R’ X and Y have the meanings as defined above, with an acyl donating agent of formula Z-C0-(G]-C6)-alkyl, Z-CO-halogen-(Ci-C3)-alkyl, Z-CO-0-(Ci-C3)-alkyl, or Z-S02-(Ci-C3)-aIkyl wherein Z is an activating group, e.g. a halogen or anhydride , or with an isocyanate.
The compounds of general formula I* can be manufactured by reacting a compound of formula IF
COOH
wherein R\ R’\ R’\ R’’ R’'‘ and n have the above meanmgs
with an amine of formxila H2N-R’, wherein R’ has the above meaning, to obtain a
compound of formula la"*

(la’)

or, alternatively, reducing a compound of formula IF to the corresponding alcohol of formula IIP

(III*)

and reacting this compound with a cyanide salt to obtain a compound of formula lb*

(lb*)

or, alternatively,
reacting a compound of formula IV"*

(iv’)

wherein X is halogen, with a cyanide salt, to obtain a compound of formula Ic'*"

ilc*)

or, alternatively, reacting a compound of formula V'*'

(V*)

with an acylating agent of formula Y-C0-(Ci-C6)-aIlcyl or Y'-S02-(Ci-C6)-alkyl, wherein Y and Y' represent an activating group, e.g. a halogen, to obtain a compound of formula Id*

(Id*)

wherein R* has the above meanings.
In accordance with the present invention, scheme 1 shows examplary routes to com¬pounds of the formula I, all starting from a compound of formula V. The reaction of a compound of formula V with a compound of formula VI [Ikuta et al., J. Med. Chem. 30:1995 (1987)] to obtain the intermediate of formula Ilia, maybe in inert solvents like dichloromethane, ethyl acetate or ethers in the presence of a base like triethylamine or carbonate and at a temperature in the range of from 0°C to 25°C. Cyclisation of the intermediate 2,4-dihalo-N-acyl derivative to the p’Trolidone Ilia may be with bases like sodium or potassium hydroxide in inert solvents like dichloromethane or ethers at a temperature of from 0°C to 25°C. Intermediates II wherein R* is H, i.e. compounds of formula Ila, are prepared by reacting a compound of formula V with 6,6-dimethyl-5,7-

dioxa-spiro[2,5]octane-4,8-dione, as described by Danishefsky et al. [J. Amer.Chem. Soc. 97:3239(1975)].
Scheme 1
hal 1) hal-CHjCHj-CH ‘hal

Another method to prepare compounds of formula I involves cross-coupling reactions of arylstannanes [Lam et al., Tetrahedron Lett. 43:3091 (2002)], arylboronates [Lam et al., Synlett 5:674 (2000); Chan et al, Tetrahedron Lett. 39:2933 (1998)] or aryl haUdes [Buch-wald et al., J. Amer. Chem. Soc. 118:7215 (1996)] with the corresponding pyrroHdones (scheme 2).
Scheme 2

R’-’' ' VIII
wherein LG is halogen, e.g. CI, Br or I, or SnRs or B(0H)2.
In accordance with the present invention, a possibility to prepare compounds of general formula V, wherein -X-Y- is -CH2-O-, i.e. compounds of formula Va, is shown in scheme 3: The intermediates of formula XII are accessible through nucleophilic substitution of aromatic nitro compounds of formula XI containing p-substituted leaving groups with benzylic alcohols of formula X. Leaving groups in para-position can be, e.g., halogens (F, CI, Br, I), tosylates, mesylates or triflates. These substitution reactions can be conducted neat or in inert solvents like for example toluene or xylene. A preferred reaction

temperature is in the range of from 50°C to 150°C. Alternatively, compounds of formula XII can be prepared by WiEiamson-ether synthesis, starting from p-nitrophenols XIV and benzylic halides, tosylates, mesylates or triflates of formula XIII. Bases used can be, e.g. alcoholates or carbonates (sodium, potassium or cesium carbonate). Examples for solvents include lower alcohols, acetonitrile or lower ketones at a temperature in the range of from 20°C to reflux temperature. Another approach is the Mitsunobu-coupling of benzylic alcohols with p-nitrophenols. The reaction is done as usual in inert solvents like for example diethyl ether or tetrahydrofurane, using dialkyl-azo-dicarboxylates in the presence of phosphines (for example tributyl- or triphenyl-phosphine).
The key intermediates of formula XII are reduced to the amino compounds of formula Va using catalytic hydrogenation, like, e.g. using platinum on charcoal as the catalyst in lower alcohols, ethyl acetate or tetrahydrofurane. An alternative is the reduction of the nitro-group by metals lilce iron, tin, or zinc in acidic media like diluted hydrochloric acid or acetic acid. Metals can also be replaced by metal salts lilce, e.g., tin-(II)-chloride).
Scheme 3

R!'‘ .CH,OH ,_r’rv’°"‘'-°
i.2
XIII
R
XIV
+
wherein LG is a leaving group, e.g. halogen and OTf, or OH (for Mitsunobu-coupling).
In accordance with the present invention, a possibility to prepare the intermediates of formula Vb (wherein -X-Y- is -CH=CH-) and Vc (wherein -X-Y- is -CH2-CH2-) is shown in scheme 4: The intermediates of formula XVII are accessible by olefmation reac¬tion of optionally substituted aromatic aldehydes of formula XV with dialkyl (4-nitro-benzyl)-phosphonates of formula XVI in the presence of a base, like e.g. sodium hydride, yielding the corresponding nitro-olefins of formula XVII.
Scheme 4

23 O

The key intermediates of formula XVII can be reduced selectively to the amino-olefins of formula Vb using catalytic hydrogenation like e.g. using platinum on charcoal as the cata¬lyst in lower alcohols, ethyl acetate or tetrahydrofiirane as the solvent, or, by metals or metal salts, lilce e.g. tin-(II)-chloride. The amino derivatives of formula Vc can be obtained directly fi-om the nitro derivatives of formula XVII or fi:om the amino-olefins of formula Vb by hydrogenation using palladium on charcoal as the catalyst in lower alcohols, ethyl acetate or tetrahydrofiirane as the solvent.
Intermediates II can be transformed into compounds of formula I using standard procedures. The acids II are activated via acid chloride (thionyl chloride or oxalyl chloride) or with DCC, EDC etc. and subsequently coupled with the amine R’-NH2. Alternatively, the corresponding alkyiesters can be transformed to intermediates II by aminolysis by ammes of formula R’-NH2.
Intermediates III can be transformed into the desired compounds I wherein R is CN, i.e. compounds of formula lb, by reaction with sodium or potassium cyanide in solvents like N,N-dimethylformamide, acetone or acetonitrile at a temperature in the range of from 20°C to 140°C. Catalytic amounts of sodium or potassium iodide can be added to speed up "the"reaction (scheme 5).
Scheme 5

III

Compounds of formula IV can be obtained starting from acid derivatives of formula II by nucleophilic migrations from a carbon to a nitrogen atom, such as e.g. by Hofmann or Curtius rearrangement, via the formation of the corresponding isocyanate and its treat¬ment with suitable alcohols delivering the protected amino group, methods known per se from the literature (scheme 6). For the treatment of the intermediate isocyanate, alcohols are selected which yield the typical carbamates used as amine protecting groups, such as e.g. tert-butoxycarbonyl, benzyloxycarbonyl, or fluorenylmethoxycarbonyl. Their cleavage to the amine follows the protocols which are well known in the literature. The farther transformation to compounds of formula I can be performed by standard procedures, such as e.g. by reaction with activated acyl derivatives, e.g. acyl halogenides or anhydrides, or by condensation reactions of the acid using e.g. carbodiimides as condensation reagent, or by isocyanates.
Scheme 6

NH-PG
»- IV
For the preparation of enantiopure derivatives of formula IV, an alternative route can be followed (scheme 7). Basically, the protocol follows the conditions described by Freidinger et al. [J. Org. Chem. 47:104-109 (1982)] where the aniline derivative of formula V is acyla-ted by an N-protected methionine derivative in its racemic or optically active form by standard conditions of condensation reactions to give compounds of formula XIX. Methylation with methyliodide or trimethyl-sulfonium or trimethylsulfoxonium salts and treatment of the resulting dimethyl-sulfonium salt with base, such as e.g. sodium hydride or lithium or potassium bis(trimethylsilyl)amide, in solvents inert under these conditions, e.g. THF, dichloromethane or N,N-dimethylformamide, yield the cyclised N-protected product of formula XX. Another variation of this cyclisation procedure is described in EP 985,665 which refers to a process for the preparation of 3-amino-2-oxo-pyrrolidines.
Scheme 7

gXHg
HOOC N H
XX

-X-Y- = -CH2-O-: R"'
hydrogenolysis R’*\X’’N’/~~-NH-PG
XX -« I I _
alkylation HC'l’’’R’ ‘‘

NHR -X-Y-=-CH2-O-: I J ,
hydrogenolysis R’\’;*!K’N’
HO V’ -°
NHR"
alkylation
-R"
Id

In compounds of formula I or XX where -X-Y- has the meaning of-CHz-O-, the op¬tionally substituted benzyl residue can function as a transient group which can be cleaved by hydrogenolysis. The resulting phenols Id and XXa can then be re-alkylated by a dif¬ferent benzyl group under the aforementioned conditions. As known to those skilled in the art, this process is only possible on condition that R and PG are representing groups that are stable under the aforementioned reaction conditions for the hydrogenolysis and alkylation reaction.
Compounds of general formula I can also exist in optical pure form. There ist the possibility to start with enantiopure compounds from the chiral pool, like e.g. (R)- or (S)-methionine. In other cases, separation into antipodes can be affected according methods known per se, either preferably at an early stage of the synthesis starting with compounds of formula II by salt formation with an optically active amine such as, for example, (-f-)- or (-)-l-phenylethylamine and separation of the diastereomeric salts by fractional crystallisation or preferably by derivatisation with a chiral auxiliary substance such as, for example, (+)- or (-)-2-butanol, (+)- or (-)-l-phenylethanol, or {+)- or (-)-menthol and separation of the diastereomeric products by chromatography and/or crystallisation and

subsequent cleavage of the bond to the chiral auxiliary substance. In order to determine the absolute configuration of the pyrrolidinone derivative obtained, the pure diastereo-meric salts and derivatives can be analysed by conventional spectroscopic methods, with X-ray spectroscopy on single crystals being an especially suitable method.
The Active Compounds are, as already mentioned above, monoamine oxidase B inhibitors and can be used for the treatment or prevention of diseases in which MAO-B inhibitors might be beneficial. These include acute and chronic neurological disorders, cognitive disorders and memory deficits. Treatable neurological disorders are for instance traumatic or chronic degenerative processes of the nervous system, such as Alzheimer's disease, other types of dementia, minimal cognitive impairment or Parkinson's disease. Other indica¬tions include psychiatric diseases such as depression, anxiety, panic attack, social phobia, schizophrenia, eating and metabolic disorders such as obesity, as well as the prevention and treatment of withdrawal syndromes induced by abuse of alcohol, nicotine and other addictive drugs. Other treatable indications maybe peripheral neuropathy caused by can¬cer chemotherapy (WO 97/33,572), reward deficiency syndrome (WO 01/34,172), or the treatment of multiple sclerosis (WO 96/40,095), and other neuroinflammatory diseases.
The Active Compounds are especially useful for the treatment and prevention of Alzheimer's disease and senile dementia.
The pharmacological activity of the compounds was tested using the following method:
The cDNAs encoding human MAO-A and MAO-B were transiently transfected into EBNA cells using the procedure described by Schlaeger and Christensen [Cytotechnology 15:1-13 (1998)]. After transfection, cells were homogenised by means of a Polytron homogenizer in 20 mM Tris HCl buffer, pH 8.0, containing 0.5 mM EGTA and 0.5 mM phenylmethane-sulfonyl fluoride. Cell membranes were obtained by eentrifugation at 45,000 x g and, after two rinsing steps with 20 mM Tris HCl buffer, pH 8.0, containing 0.5 mM EGTA, mem¬branes were eventually re-suspended in the above buffer and aliquots stored at -80°C until use.
MAO-A and MAO-B en2ymatic activity was assayed in 96-well-plates using a spectro-photometric assay adapted from the method described by Zhou and Panchuk-Voloshina [Analytical Biochemistry 253:169-174 (1997)]. Briefly, membrane ahquots were incubated in 0.1 M potassium phosphate buffer, pH 7.4, for 30 min at 37°C containing different con¬centrations of the compounds. After this period, the enzymatic reaction was started by the addition of the MAO substrate tyramine together with 1 U/ml horse-radish peroxidase

(Roche Biochemicals) and 80 |iM ]V-acet}d-3,7-dihydroxyphenoxazine (Amplex Red, Molecular Probes). The samples were further incubated for 30 min at 37°C in a final volume of 200 |il and absorbance was then determined at a wavelength of 570 nm using a SpectraMax plate reader (Molecular Devices). Background (non-specific) absorbance was determined in the presence of 10 |iM clorgyline for MAO-A or 10 jiM L-deprenyl for IvlAO-B. IC50 values were determined from inhibition curves obtained using nine inhibitor concentrations in dupHcate, by fitting data to a four parameter logistic equation using a computer program.
The compounds of the present invention are specific MAO-B inhibitors. The IC50 values of preferred Active Compounds as measured in the assay described above are in the range of 1 |iM or less, typically 0.1 \iM or less, and ideally 0.02 ‘M or less.
The Active Compounds can be used as medicaments, e.g. in the form of pharmaceutical preparations. The pharmaceutical preparations can be administered orally, e.g. in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions. However, the administration can also be effected rectally, e.g. in the form of suppositories, or parenteraUy, e.g. in the form of injection solutions.
The Active Compounds can be processed with pharmaceutically inert, inorganic or organic carriers for the production of pharmaceutical preparations. Lactose, corn starch or derivatives thereof, talc, stearic acid or its salts and the like can be used, for example, as such carriers for tablets, coated tablets, dragees and hard gelatine capsules. Suitable carriers for soft gelatine capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like; depending on the nature of the active substance no carriers are, how¬ever, usually required in the case of soft gelatine capsules. Suitable carriers for the produc¬tion of solutions and syrups are, for example, water, polyols, sucrose, invert sugar, glucose and the like. Adjuvants, such as alcohols, polyols, glycerol, vegetable oils and the like, can be used for aqueous injection solutions of water-soluble salts of Active Compounds, but as a rule are not necessary. Suitable carriers for suppositories are, for example, natural or hardened oils, waxes, fats, semi-liquid or liquid polyols and the like.
In addition, the pharmaceutical preparations can contain preservatives, solubilizers, stabi¬lizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They may also contain other therapeutically valuable substances.

As mentioned earlier, medicaments containing an Active Compound and a therapeutically inert excipient are also an object of the. present invention, as is a process for the pro¬duction of such medicaments which comprises bringing one or more Active Compound and, if desired, one or more other therapeutically valuable substances into a galenical dosage form together with one or more therapeutically inert carriers.
The dosage can vary within wide limits and will, of course, be fitted to the individual requirements in each particular case. In general, the effective dosage for oral or parenteral administration is between 0.01-20 mg/kg/day, with a dosage of 0.1-10 mg/kg/day being preferred for all of the indications described. The daily dosage for an adult human being weighing 70 kg accordingly lies between 0.7-1400 mgper day, preferably between 7 and 700 mg per day.
The following examples are provided for illustration of the invention. They should not be considered as limiting the scope of the invention, but merely as being representative there¬of The abbreviation „RT" means „room temperature".
Example 1: (RS)-l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidine-3-carbonitrile
a) (RS)-N-(4-Benzyloxy-phenyl)-2,4-dibromo-butyTamide
A solution of 12.8 g (64.2 mmol) 4-benzyloxyaniline and 9.74 g (96.3 mmol) triethylamine in 125 ml dichloromethane is cooled to 0°C. 20.4 g (77.1 mmol) of 2,4-dibromobutyryl chloride [Ikuta et al., J. Med. Chem. 30:1995 (1987)] is slowly added over a period of 45 min. The reaction mixture is stirred for additional 15 min, then hydrolysed with 100 ml of water. The insoluble precipitate is filtered off and the organic phase is washed successively with a saturated solution of sodium hydrogen carbonate and water. After drying and eva¬poration, the crude product is subjected to chromatography (silica gel, dichloromethane) to yield 6.1 g (22 %) of a colorless soUd. Mp = 139.5-142 °C.
b) (RS)-l-(4-Benzyloxy-phenyl)-3-bromo-pyrrolidin-2-one
6.1 g (14.3 mmol) (RS)-N-(4-benzyloxy-phenyl)-2,4-dibromo-butyTamide and 0.1 g of Dowex 2X10 are suspended in 50 ml dichloromethane. 7 ml of a 50% aqueous sodium hydroxide solution is slowly added under vigorous stirring. The resulting reaction mixture is stirred overnight at RT, then poured into 25 ml of cold water. The organic phase is separated, dried and evaporated. The crude material is recrystallised from ethyl acetate to yield 1.72 g (35 %) of a brownish soUd. Mp = 125-126 °C.
c) (RS)-l-(4-Benzyloxy-phenyl)-2-oxo-p}TroUdine-3-carbonitrile
300 mg (0.87 mmol) of (RS)-l-(4-benzyloxy-phenyl)-3-bromo-pyrroHdin-2-one is dissolved in 5 ml N,N-dimethylformamide. 64 mg (1.3 mmol) sodium cyanide and 13 mg

0.09 mmol) sodium iodide are added and the suspension stirred for 10 min. at 120 °C. 'he reaction mixture is treated with water and extracted with ethyl acetate to yield 33 mg 13 %) of a colorless solid. MS: m/e = 293.3 (M+ H)"".
ixample 2: (RS)-1 -[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid methylamide
.) l-(4-Benzyloxy-phenyl)-pyrrolidin-2-one
'.03 g (101.9 mmol) 4-benzyloxyaniline and 9.1 ml (119.2 mmol) gamma-butyro-lactone ire treated with 3ml concentrated hydrochloric acid. The mixture is heated 20 hours to .60°C, then 5.5 hours to 200°C. After cooling, the mixture is extracted with 250 ml ethyl icetate, washed with saturated aqueous sodium hydrogencarbonate and dried. Evapora-ion of the solvent and recrystallisation from diethyl ether yields 8.4 g (31 %) of a )rownish solid. MS: m/e = 267 (M"‘). )) l-(4-Hydroxy-phenyl)-pyrrolidin-2-one
5.2 g (23.2 mmol) l-(4-benzyloxy-phenyI)-pyrrolidin-2-one is dissolved in 200 ml THF. 3 irops of acetic acid are added and the solution is hydrogenated for 5 hours at RT and nor-nal pressure in presence of 0.62 g palladium 10 % on charcoal. Filtration and concentra-lion gives a semisolid material. Chromatography (silica gel, dichloromethane / methanol ?5 : 5) yields 2.73 g (66 %) of a brownish soHd. MS: m/e = 175.9 (M-H). z) l-[4-(3-Fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one
A. mixture of 2.73 g (15.4 mmol) of l-(4-hydroxy-phenyl)-pyrrolidin-2-one, 3.2 g (16.9 mmol) of 3-fluorobenzylbromide and 4.26 g (31 mmol) of potassium carbonate in 100 ml of 2-butanone is heated at 80°C for 18 hours. After cooling to RT, the reaction mixture is treated with water and ethyl acetate. The organic layer is separated, dried over magnesium sulfate and evaporated under reduced pressure. The solid residue is cr)'stallised from ether to yield 3.86 g (88% of theory) of l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrroHdin-2-one as a colorless solid. MS: m/e = 286.0 (M+ H)’.
d) l-[4-(3-Fluoro-benzylox}0-phenyl]-2-oxo-pyrrolidine-3-carboxyHc acid ethyl ester 370 mg (15.4 mmol) sodium hydride is suspended in 20 ml THF and 911 mg (7.7 mmol) diethylcarbonate is added. The suspension is heated to reflux temperature, A solution of 2.0 g (7.0 mmol) l-[4-(3-Fluoro-benzyIoxy)-phenyl]-pyrrolidin-2-one in 10 ml THF is slowly added into the boiling solution. The mixture is boiled for another 5 hours, then hydrolysed with cold water and washed successively with water, saturated sodium hydro¬gencarbonate solution, water and saturated sodium chloride solution. Chromatography (siKca gel, dichloromethane / ethyl acetate) yields 1.3 g (52 %) of a yellowish semisolid. MS: m/e = 358.2 (M+ H)’.

s) (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyi]-2-oxo-pyTrolidine-3-carbox)dic acid methyl-amide
300 mg (0.84 mmol) l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid ethyl ester is dissolved in 2 ml N,N-dimethylformamide. 0.17 ml (4.2 mmol) of a 33 % solution of methylamine in ethanol is added. The reaction vessel is tightly stoppered and heated to 120°C for 24 hours. Addition of water precipitates the crude material. Chroma¬tography (silica gel, dichloromethane / methanol) yields 41 mg (14 %) of a yellowish solid. MS: m/e = 343.2 (M+ H)+.
Examples: (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide
a) l-(3-Fluorobenzyloxy)-4-nitro-benzene
A mixture of 5.04 g (40 mmol) 3-fluorobenzyl alcohol and 1.29 g (4mmol) tris-(dioxa-3,6-heptyl)amine is treated with 2.47 g (44 mmol) of potassium hydroxide. The mixture is stirred at RT for 10 min, then 5.55 g (44 mmol) of 4-fluoro-nitrobenzene is slowly added through a dropping funnel. The mixture is kept for 45 min at 80°C, cooled to RT and di¬luted with about 75 ml water. Extraction with ethyl acetate and washing with 2M aqueous hydrochloric acid yields a yellowish organic phase, which is dried and evaporated. The residue is recrystallised from methanol to give 6.07 g (61 %) of the title compound. Yellow crystals, mp = 104-105 °C.
b) 4-(3-Fluoro-benzyloxy)-phenylamine
3 g (12.1 mmol) of l-(3-fluorobenzyloxy)-4-nitro-benzene is dissolved in 125 ml of methanol. 150 mg of Pt 5% on charcoal is added and hydrogenation done under normal pressure for about 17 h. The catalyst is filtered and the solution evaporated to yield 2.51 g (95%) of crude brownish material. MS: m/e = 218.4 (M+H)"‘.
c) (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrroHdine-3-carbox)dic acid
A solution of 561 mg (2.6 mmol) 4-(3-fluoro-benzyloxy)-phenylamine and 448 mg (2.6 mmol) 6,6-dimethyl-5,7-dioxa-spiro[2,5]octane-4,8-dione in 2ml dichloromethane is refluxed for 16 hours. 5 ml of diethylether is added and the precipitate filtered off to yield 485 mg (57 %) of a colorless solid. MS: m/e = 330.2 (M+H)’.
d) (RS)-l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrroHdine-3-carboxylic acid amide
300 mg (0.91 mmol) (RS)-l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrroHdine-3-carb-
oxylic acid is dissolved in 2 ml dichloromethane plus 2 drops of N,N-dimethyl-formamide.
The solution is cooled to 0 °C and treated with 173 mg (1.37 mmol) oxalyl chloride. After
1 hour at 0 °C the solvent is removed under vacuum at RT. The residue is taken up in 1 ml dichloromethane and slowly added to a mixture of 2 ml THF and 5 ml concentrated

ammonia. Stirring is continued for 1 hour at RT. Evaporation of the solvents and dilution with water yields a precipitate, which is filtered off. Recrystallisation fi-om methanol yields 112 mg (37 %) of a colorless soHd. MS: m/e = 329.2 (M+H)’.
Example 4: (RS)-l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid amide
a) l-(4-Fluorobenzyloxy)-4-nitro-benzene
The title compound is prepared in analogy to Example 3a) from 4-fluorobenzyl alcohol and 4-fluoro-nitrobenzene. Yield : 86 % of a yellowish sohd. Mp = 124-126°C.
b) 4-(4-Fluoro-benzyloxy)-phenylamine
The title compound is prepared in analogy to Example 3b) by reduction of l-(4-fluoro-benzyloxy)-4-nitro-benzene. Yield: 98 % of a red soHd. MS: m/e = 218.3 (M+H)"‘.
c) (RS)-l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylicacid
The title compound is prepared in analogy to Example 3c) from 4-(4-fluoro-benzyloxy)-phenylamine and 6,6-dimethyl-5,7-dioxa-spiro[2,5]octane-4,8-dione. Yield : 56 % of a colorless soHd. MS: m/e = 284.1 (M-CO2).
d) (RS)-l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxyUc acid amide
The title compound is prepared in analogy to Example 3d) from (RS)-l-[4-(4-fIuoro-
benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid and ammonia. Yield : 18% of a
brownish solid. MS: m/e = 329.3 (M’+ H).
Example 5: (RS)-1- [4-(4-Fluoro-benzyloxy)-phenyl] -2-oxo-p-jT:rolidine-3-carboxylic acid mefhylamide
The title compound is prepared in analogy to Example 3d) firom (RS)-l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidine-3-carboxylic acid and methylamine. Yield : 17% of a colorless solid. MS: m/e = 343.2 (M+H)"‘.
Example 6: (RS)-2-Oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid amide
a) l-(4-Trifluoromethyl-benzyloxy)-4-nitro-benzene
The title compound is prepared in analogy to Example 3a) from 4-fluoro-nitro-benzene and 4-trifluoromethyl-benzyl alcohol. Yield 82 % of a shghtly brown sohd. Mp. = 80.5 -81.5 °C.
b) 4-(4-Trifluoromethyl-benzyloxy)-phenylamine

The title compound is prepared in analogy to Example 3b) by reduction of l-(4-tri-fluoromethyl-benzyloxy)-4-nitro-benzene. Yield : 91 % of a yellowish sohd. MS: m/e = 268.3 (M+H)-".
c) (RS)-2-Oxo-l-[4-(4-trifiuoromethyl-benzyloxy)-phenyl]-pyrrohdine-3-carboxylic acid The title compound is prepared in analogy to Example 3c) from 4-(4-trifluoro-methyl-benzyloxy)-phenylamine and 6,6-dimethyl-5,7-dioxa-spiro[2,5]octane-4,8-dione. Yield : 37 % of a colorless soHd. MS: m/e = 380.1 (M+H)’.
d) (RS)-2-Oxo-l-[4-(4-trifIuoromethyl-benzyIoxy)-phenyl]-pyrrolidine-3-carboxylicacid amide
150 mg (0.4 mmol) (RS)-2-oxo-l-[4-(4-trifluoromethyI-benzyloxy)-phenyl]-pyrrolidine-3-carboxyhc acid is dissolved in 4 ml THE. 59 mg (0.43 mmol) of 1-hydroxybenzotriazole and 80 mg (0.42 mmol) of N-(3-dimethylaminopropyl)-N'-eth7l-carbodiimide-hydro-chloride is added and the reaction mixture is stirred at RT for 30 min. After cooling to 0°C 4ml of concentrated ammonia is added and the resulting mixture stirred at RT for 1 hour. Dilution with water, extraction and chromatography (silica gel, ethyl acetate) yields 15 mg (10 %) of a colorless solid. MS: m/e = 379.2 (M+H)"".
Example 7: (RS)-2-Oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid methylamide
The title compound is prepared in analogy to Example 6d) from (RS)-2-oxo-l-[4-(4-trifluoromethyl-benzyloxy)-phenyl]-pyrrolidine-3-carbox7lic acid and methylamine. Yield: 6 % of a colorless solid. MS: m/e = 393.2 (M+H)’.
Examples: (S)-N-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-acetamide
a) (S)-[l-(4-Benzyloxy-phenylcarbamoyl)-3-methylsulfanyl-propyl]-carbamic acid tert-but)'l ester
A solution of 0.57 g (2.3 mmol) of (S)-Boc-methionine in 5 ml of dichloromethane is treated at RT consecutively with 0.87 g (2.3 mmol) of 0-(benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium-hexafluorophosphate (HBTU), 0.50 g (2.1 mmol) of 4-benzyloxy-aniline hydrochloride and 0.98 ml (5.7 mmol) of N-ethyl-diisopropylamine. The reaction mixture is stirred during 1 h at RT. For the working-up, the reaction mixture is diluted with dichloromethane and treated with 20 ml of an aqueous solution of citric acid (10%). The aqueous phase is re-extracted with dichloromethane, the organic phases combined, dried over sodium sulfate and evaporated under reduced pressure. For purification, the crude material obtained is chromatographed on silica gel using a 3:1 mixture of n-hexane and etiiyl acetate as the eluent There are obtained 0.74 g (82.5% of theory) of (S)-[l-(4-

benzyioxy-phenylcarbamoyl)-3-methylsulfanyl-propyl]-carbamic acid tert-but)’l ester as a white soHd. MS: m/e = 431 (M+H)’
b) (S)-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidiii-3-yl]-carbamic acid tert-butyl ester A mixture of 0.35 g (0.81 mmol) of (S)-[l-(4-benzyloxy-phenylcarbamoyl)-3-methyl-sulfanyl-p’opyl]-carbamic acid tert-butyl ester and 8.79 g (62.0 mmol) of methyHodide is stirred at.RT for 3 d. Thereafter, the methyliodide is evaporated, the intermediate sulf-onium salt dissolved in 15 ml of THF and treated with 0.79 ml (0.79 ml) of lithium bis-(trimethylsilyl) amide (1 M solution in THF) at 0°C. After stirring at 0°C for 2 h, the reaction mixture is evaporated under reduced pressure and the solid residue is directly submitted to chromatography on silica gel using a 2:1 mixture of n-hexane and ethyl acetate as the eluent. There are obtained 0.175 mg (56% of theory) of (S)-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester as a white solid. MS: m/e = 383 (M+H)’
c) (S)-3-Amino-l-(4-benzyloxy-phenyl)-pyrrolidin-2-one hydrochloride
A solution of 137 mg (0.36 mmol) of (S)-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester in 2 ml of dioxane is treated with 0.3 ml of hydrochloric acid (37%). The solution is warmed to 45°C for 1 h forming a white suspension. For the worlc-ing-up, the reaction mixture is evaporated under reduced pressure and the solid residue is triturated with a small volume of methanol. After filtration and drying, 94 mg of (S)-3-amino-l-(4-benzyloxy-phenyl)-p"5Trolidin-2-one hydrochloride (82% of theory) are ob¬tained as a white solid. MS: m/e = 283 (M + H)"‘.
d) (S)-N-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrohdin-3-yl]-acetamide
A solution of 40 mg (0.13 mmol) of (S)-3-amino-l-(4-benzyloxy-phenyl)-pyrrolidin-2-one hydrochloride in 2 ml of dichloromethane is treated with 38 p.1 (0.28 mmol) of tri-ethylamine and cooled to 0°C. To this solution, 10 [il (0.14 mmol) of acetylchloride are added and stirring at 0°C is continued for 30 min. For the working-up, the reaction mix¬ture is treated with 2 ml of ammonium hydroxide solution, the organic phase separated, thereafter dried over sodium sulfate and evaporated under reduced pressure. For purifi¬cation, the material obtained is chromatographed on silica gel using a 95:5 mixture of di¬chloromethane and methanol as the eluent. There are obtained 31 mg (76% of theory) of (S)-N-[l-(4-enzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-acetamide as a white solid. MS: m/e = 325 (M+H)"*-.
Example 9: (S)-N-[l-(4-Benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-methanesulfGn-amide

In an anologous manner to that described in Example 8d), the reaction of (S)-3-amino-l-(4-benzyloxy-phenyl)-pyrrohdin-2-one hydrochloride with methanesulfochloride in the presence of triethylamine yields (S)-N-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-methanesulfonamide as a white soUd. MS: m/e = 361 (M+H)"*".
Example 10: (S)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide
a) In an anologous manner to that described in Example 8a) to c), the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride is obtained: Condensation of (S)-BOC-methionine and 4-(3-fluorobenzyloxy)-phenylamine [Example 3b)] by HBTU yields the (S)-{l-[4-(3-fluoro-benzyloxy)-phenylcarbamoyl]-3-methylsulfanyl-propyl}-carbamic acid tert-butyl ester as a light yellow solid; MS: m/e = 449 (M+H)"‘. The following methylation and cyclisation yields the (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert-butyl ester as a white solid; MS: m/e = 401 (M+H)"‘. The cleavage of the BOC-group yields the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrohdin-2-one hydrochloride as a white solid; MS: m/e = 301 (M+H)"".
b)lS)-N-{l-[4-(3-fluoro-benzylox}')-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide In an anologous manner to that described in Example 8d), the acetylation of the (S)-3-amino-l-[4-(3-fludro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 343 (M-l-H)"‘.
Example II: (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide,
(R)-N"{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-p}T:rolidin-3-yl}-methanesulfonamide,
(S)-N-{1 - [4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-methanesulfonamide and (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic
acid methyl ester
In an anologous manner to that described in Example 8 d), the acylation of (R)- or (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride [the (R)-isomer is obtained in analogy to the (S)-isomer as described in Example 10 a) starting from (R)-BOC-methionine] yield the following compounds:

) Reaction of the (R)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one
ydrochloride with acetylchloride yields the (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-
xo-pyrrolidin-3-yl}-acetamide as a white soHd; MS: m/e = 343 (M+H)"‘.
') Reaction of the (R)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one
lydrochloride with methanesulfochloride yields the (R)-N-{l-[4-(3-fluoro-benzyloxy)-
ihenyl]-2-oxo-pyrrolidin-3-yl}-methanesulfonamide as a white solid; MS: m/e = 377
M-hH)"'.
:) Reaction of the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one
lydrochloride with methanesulfochloride yields the (S)-N-{l-[4-(3-fluoro-benzyloxy)-
)henyl]-2-oxo-pyrrohdin-3-yl}-methanesulfonamide as a white solid; MS: m/e = 377
M+Hf.
i) Reaction of the (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one
lydrochloride with methyl chloroformate yields the (S)-{l-[4-(3-fluoro-benzyloxy)-
3henyl]-2-oxo-p}Trolidin-3-yl}-carbamic acid methyl ester as a white solid; MS: m/e = 359
:M+H)"'.
Example 12: (R)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yI}-formamide
A. mixture of 188 mg (18 mmol) of acetic anhydride and 107 mg (23 mmol) of formic acid is prepared at 0°C, thereafter, heated to 60°C for 2 hours.After cooHng to RT, the mixture is diluted with 1 ml of tetrahydrofiirane and a solution of 213 mg (7 mmol) of (R)-3-amino-l-[4-(3-fiuoro-benzyloxy)-phenyl]-pyrrolidin-2-one in 2 ml of dichloromethane, beforehand prepared from the corresponding hydrochloride by treatment with triethylamine, is added. After the addition a white suspension is formed which is stirred at RT for 1 hour. For the working-up, the reaction mixture is treated with dichloromethane and water, then, the organic layer is separated, dried over sodium sulfate and evaporated. There are obtained 215 mg (92% of theory) of (R)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyTrolidin-3-yl}-formamide as a white soHd; MS: m/e = 329 (M+H) .
Example 13: (S)-N-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-formamide
In an analogous manner to that described in Example 12, the reaction of (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one with a mixture of acetic anhydride and formic acid yields the title compound as a white soHd; MS: mZe = 329 (M+H) .
Example 14: (R)-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrroUdin-3-yl}-urea

A solution of 250 mg (0.7 mmol) of (R)-3-amino-l-[4-(3-fluoro-benzyIoxy)-phenyl]-pyrrolidin-2-one hydrochloride and 294 mg (2.2 mmol) of N-ethyl-diisopropylamine in 2 ml of N,N-diinethylformamide is cooled to 0°C and treated with 267 mg (2.2 mol) of trimethylisocyanate. The reaction mixture is left to warm to RT and stirring is continued for 2 days. For the working-up, the suspension is evaporated under reduced pressure. The crude product is triturated in water, then the recovered solid material triturated a second time in a mixture of ethyl acetate and a saturated solution of sodium hydrogencarbonate. The remaining solid is collected on a filter funnel to give, after drying under high vacuum, 155 mg (61% of theory) of (R)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-urea as a white solid; MS: m/e = 344 (M+H)"‘.
Example 15: (S)-{l-[4-(3-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidLn-3-yl}-urea
In an analogous manner to that described in Example 14, the reaction of (S)-3-amino-l-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one trimethylisocyanate yields the title compound as a white solid; MS: m/e = 344 (M+H)"*".
Example 16: (S)-N-{l-(S)-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide
a) (S)-[l-(4-Hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester
In an analogous manner to that described in Example 2b), the hydrogenolysis of the.(S)-[l-(4-benzyloxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester [Example 8 b)] using palladium on carbon as the catalyst yields the title compound as a white solid in quantitative yield; MS: m/e= 291 (M-H)"‘.
b) (S)-{l-[4-(4-Fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert-
butyl ester
In an analogous manner to that described in Example 2c), the alkylation of the (S)-[l-(4-hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acid tert-butyl ester with 4-fluorobenzylbromide in presence of potassium carbonate yields the title compound as a white solid; MS: m/e= 401 (M+H)’.
c) (S)-3-Amino-l-[4-(4-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride
In an analogous manner to that described in Example 8c), the cleavage of the BOC-group of the (S)-{l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-carbamic acid tert-butyl ester yields the title compound as a white sohd; MS: m/e= 301 (M-f-H) .
d) (S)-N-{l-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide

In an anologous manner to that described in Example 8 d), the acetylation of the (S)-3-amino-l-[4-(4-fluoro-benzyIoxy)-phenyl]-p}arohdin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 343 (M+H)"‘.
Example 17: (S)-N-{l-(S)-[4-(2,6-Difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yI}-acetamide
a) (S)-{l-[4-(2,6-Difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert-
butyl ester
In an analogous manner to that described in Example 2c), the alkylation of the (S)-[l-(4-hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acidtert-butyl ester [Example 16 a)] with 2,6-difluorobenzylbromide in presence of potassium carbonate yields the title compound as a white solid; MS: m/e= 419 (M+H)"‘.
b) (S)-3-Amino-l-[4-(2,6-difluoro-benzylox}')-phenyl]-pyrrolidin-2-one hydrochloride In an analogous manner to that described in Example 8c), the cleavage of the BOC-group of the (S)-{l-[4-(2,6-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acid tert-butyl ester yields the title compound as a white solid.
c) (S)-N-{l-[4-(2,6-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide
In an anologous manner to that described in Example 8 d), the acetylation of the (S)-3-amino-l-[4-(2,6-difluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 361 (M+H)'‘.
Example 18: (S)-N-{l-[4-(3,4-Difluoro-benzylox)'-)-phenyl]-2-oxo-pyrroHdiii-3-yl}-acetamide
a) (S)-{l-[4-(3,4 -Difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamic acidtert-
butyl ester
In an analogous manner to that described in Example 2c), the alkylation of the (S)-[l-(4-hydroxy-phenyl)-2-oxo-pyrrolidin-3-yl]-carbamic acidtert-butyl ester [Example 16 a)] with 3,4-difluorobenzylbroniide in presence of potassium carbonate yields the title compound as a white solid; MS: m/e= 419 (M+H)"*".
b) (S)-3-Amino-l-[4-(3,4-difluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride In an analogous manner to that described in Example 8c), the cleavage of the BOC-group of the (S)-{l-[4-(3,4-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-carbamicacid tert-butyl ester yields the title compound as a white solid; MS : m/e= 319 (M+H)"*".
c) (S)-N-{l-[4-(3,4-difluoro-benzyloxy)-phenyl]-2-oxo-pyrrohdin-3-yl}-acetamide

In an anologous manner to that described in Example 8 d), the acet}'lation of the (S)-3-amino-l-[4-(3,4-difluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride yields the title compound as a white solid; MS: m/e = 361 (M+H)'*'.
Example A: Tablets
Tablets of the following composition are produced in a conventional manner:

mg/Tablet
Active ingredient 100
Powdered lactose 95
White corn starch 35
Polyvinylpyrrolidone 8
Na carboxymethylstarch 10
Magnesium stearate 2
Tablet weight 250
Example B: Tablets
Tablets of the following composition are produced in a conventional manner:
mg/Tablet
Active ingredient 200
Powdered lactose 100
White corn starch 64
Polyvinylpyrrolidone 12
Na carboxymethylstarch 20
Magnesium stearate 4
Tablet weight 400
Example C: Capsules
Capsules of the following composition are produced:

mg/Capsule
Active ingredient 50
Crystalline lactose 60
Microcrystalline cellulose 34
Talc 5
Magnesium stearate 1

Capsule fill weight 150
The active ingredient having a suitable particle size, the crystalline lactose and the micro-crystalline cellulose are homogeneously mixed with one another, sieved and thereafter talc and magnesium stearate are admixed. The final mixture is filled into hard gelatine capsules of suitable size.
Example D: Injection solution
An injection solution may have the following composition and is manufactured in usual manner:
Active substance 1.0 mg
1 N HCl 20.0 III
acetic acid 0.5 mg
NaCl 8.0 mg
phenol 10.0 mg
INNaOH q.s. adpH5
H2O q.s. ad 1 ml

WE CLAIM:
1, A pompom of the formula I

wherein
X-Yis -CH2-CH2-, -CH=CH- or ;Hj-O-;
R', R;' and R ; independently from each other are selected from the group consisting of
hydrogen, halogen, cyan, (CrC6)-aIkyl, halogen-(Ci-C6)-alkyl, (Ic-Q)-alkoxy or halogen-
(Ic-Qs)-alkoxy; R;\ R; and R; independently from each other are selected from the group consisting of
hydrogen and halogen; R;* is hydrogen, halogen or methyl R' is hydrogen;
R* is-CONHR;-Nor-NHR*; R* is hydrogen or (CrC3)-aIkyl; and R' is -CO-H, -CO'(Ic-Q)-alkyl, .CO-halogen-(CrC3)-a]k)d, -C0-0-(Ci-C3)-aIkyl, -CO-NH2
or -S02-(Ci-C5)-alkyl; as well as individual isomers, racemic or non-racemic mixtures thereof.
2.The compound as claimed in claim-1, wherein X-Y is -CH2-CH2-.
3. The compound as claimed in claim 1 ,wherein R; R*"; and R;*; independently from each other are selected from the group consisting of hydrogen, halogen, methyl, halogenmeth';, cyan, methoxy or halogen-methoxy.
4. The compound as claimed in claim 1, wherein R;S R;; and R; are hydrogen.
5. The compound as claimed in claim 1, wherein R** is hydrogen.
6. The compound as claimed in claim 1, wherein R* is -CONHR', wherein R; is hydrogen or (Ci-C3)-alkyd.

7. The compound as claimed in claim 1 ,wherein R* is -CN.
8. The compound as claimed in claim 1, wherein R* is -NHR; herein R; is -CO-H, -CO-(Ci-C6)-alkyl, -CO-halogen-(Ci-Ca)-alky], -CO-0-{Ci-Cs)- -CO-NH2 or -S02-(C,-Q)-alkyd.
9. The compound as claimed in claim 1, wherein the compound has (S)-configuration

10. The compound as claimed in claim wherein the compound has (R)-configuration.
11. The compound as claimed in claim wherein the compound is selected from (RS)-l-(4-ben2yio3cy-phenyi)'2-oxo-pyrrolidine-3-carbonitrile,
(RS)-l- [4-(3-fluoro-bciizyloxy)-phenyl] -2-oxo-pyrrolidiQe-3-carboxylic add methylamide, (RS)-l-[4-(3-fluoro-ben27loxy)-phenyi]-2-oxo-pyrrolidine-3-carboacyiic acid amide, (RS)-l-[4-(4-fluoro-benzyioxy)-phenyl]-2-os:o-pyrrolidine-3-carbo3jyIic acid amide, (RS)-l-(4-(4-fluoro-benzyloxy)-phenyl] -2-oxo-pyrrolidine-3-carboxylic acid methylamide, (RS)-2-oxo-l-[4-(4-trifluoromethyl-benzylo3cy)-phenyI]-pyrroIidine-3-carboxyUc add amide, (RS)-2-oxo-l-[4-(4-tri£luoromethyI-benzyloxy)-phenyl]-pyrrolidine-3-carboryiicadd
methylamide, (S)-N-[l-(4-ben2yloxy-phenyi)'2-oxo-pyrroIidin-3-yl]-acetamide, (S)-N-11 - (4'benzyioxy-phenyI)-2-oxo-pyirolidin-3-yI] -mcthanesxilfonamidc, (S)-N-{ 1 - [4-(3-auoro-b enzjdoxy)-phen3d] -2-oxo-pyrrclidin-3 -;}-acetamide, (R)-N-{l-[4-(3-fluoro-ben2yioxy)-phenylI-2-oxo-pyrrolidin-3-yI}-acetamide, (R)-N-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yi}-methanesulfonaniide, (S)-N-{ 1 - [4-(3-fiuoro-benzyiQxy)-phenyl] -2-oxo-pyrrolidin-3-yi}-methanesuIfonamide, (S)-{l-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yi}-caibamic acid methyl ester, (R) -N-{ 1 - [4-(3-fluoro-benzyloxy) -phenyl) -2-oxo-pyrrolidin-3-yl} -formamide, (S)-N-{l-[4-(3-fluoro-ben2yioxy)-phen54]-2-oxo-pyrrolidin-3-yl}-formative, (R)-{l-[4-(3-fluoro-ben2yioxy)-phenyI]-2-oxo-pyrroIidin-3-yI}-urea, (S)-{l-[4-(3-fluoro-benzyloxy)-phenylI-2-oxo-pyxTolidin-3-yl}-U)rea, (S)-N-{l-(S)-[4-(4-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-acetamide, (S)-N-{ l'(S)- [4-(2,6-difluoro-ben2yloxy)-phenyl]-2-oxo-pytrQlidin-3-yI}-acetamide and (S)-N-{l-[4-(3,4-difluoro-benzjioxy)-phen'yI]-2-oxo-pyrroIidin-3-)4}-acetamide.
12. A process for the preparation of compounds of formula I as claimed in claim wherein
(a)R*isCONHR*
comprising reacting a compound of formula II

(H)

wherein R\ R;-\ R'•; r', R;, R», R»*, R>, X and Y have the meanings as defined above and R* is hydrogen, with thionyl chloride or oxalyl chloride, or with DCC or EDC, and subsequent coupling
with an amine of formula H2N-R; wherein R* has the meaning.as defined in daim 1;
(b)R*isCN
comprising reacting a compound of formula III
(HI)
wherein R; R*; R;-;, R", R;, R;, R", R', X and Y have the meanings as defined above and Hal is
halogen,
with sodium or potassium cyanide in N,N-dimethylformamide, acetone or acetonitrile at a temperature
in the range of from 20°C to 140°C, and optional catalytic amounts of sodium or potassium iodide; or
(c)R*isNHR*
comprising reacting a compound of formula IV

R';

x.;iA,.o (IV)

wherein R\ R;"\ R;■; R", R;, R;, R", R', X and Y have the meanings a$ defined above, with an acyl donating agent of formula Z-CO-H, Z-CO-(Ci-C6)-alkyl, Z-CO-halogen-CCi-Cj)-alkyi, Z-CO-0-(Ci-C3)-alkyi, or Z-S02-(Ci-C3)-a]kyl wherein Z is an activating group, eg. a halogen or anhydride, or with an isocyanate.

13. The compound of the formula I* as claimed in claim 1,

Wherein
R' is halogen, halogen-(Ci-C6)-alkyl, cyano, (Ci-C6)-alkoxy or halogen-(Ci-C6)-alkoxy;
R , R , R and R independently from each other are selected from the group
consisting of hydrogen and halogen;
R' is hydrogen;
R; is-CONHR; -CH2CN-CN or-NHR;
R; is hydrogen or CpCs-alkyl;
R; is C0-(CrC6)-alkyl or-S02-(Ci-C6)-alkyl; and
N is 0, 1, 2 or 3; as well as individual isomers, racemic or non-racemic mixtures thereof
14. A pharmaceutical composition containing a compound as claimed in claim 1 or 13, and pharmaceutically acceptable excipients.

Documents:

0419-chenp-2008 abstract duplicate.pdf

0419-chenp-2008 abstract.pdf

0419-chenp-2008 claims duplicate.pdf

0419-chenp-2008 claims.pdf

0419-chenp-2008 correspondence others.pdf

0419-chenp-2008 correspondence po.pdf

0419-chenp-2008 description (complete) duplicate.pdf

0419-chenp-2008 description (complete).pdf

0419-chenp-2008 form-1.pdf

0419-chenp-2008 form-18.pdf

0419-chenp-2008 form-26.pdf

0419-chenp-2008 form-3.pdf

0419-chenp-2008 form-5.pdf

0419-chenp-2008 pct search report.pdf

0419-chenp-2008 pct.pdf

0419-chenp-2008 petition.pdf

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Patent Number

219262

Indian Patent Application Number

419/CHENP/2005

PG Journal Number

23/2008

Publication Date

06-Jun-2008

Grant Date

28-Apr-2008

Date of Filing

17-Mar-2005

Name of Patentee

F. HOFFMANN-LA ROCHE AG

Applicant Address

Inventors:

#	Inventor's Name	Inventor's Address
1	JOLIDON, Synese
2	RODRIGUEZ-SARMIENTO, Rosa Maria
3	WOSTL, Wolfgang
4	WYLER, Rene

PCT International Classification Number

C07D207/26

PCT International Application Number

PCT/EP2003/010383

PCT International Filing date

2003-09-18

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	02021319.5	2002-09-20	EUROPEAN UNION