Title of Invention

A THROMBIN RECEPTOR ANTAGONISTS OF FORMULA I

Abstract

The present invention relates to a Heterocyclic-substituted tricyclics of the formula (I) or a pharmaceutically acceptable salts thereof, wherein: n<sub>1</sub> and n<sub>2</sub> are independently 0-2; Het is an optionally substituted mono-, bi-or tricyclic heteroaromatic group; B is alkyl or optionally substituted alkenyl; R<sup>22</sup> is -COR<sup>23</sup> or a carboxy, sulfinyl, sulfonyl, sulfonamide or amino acid derivative; R<sup>23</sup> is haloalkyl; alkenyl; haloalkenyl; alkynyl; optionally substituted cycloalkyl; cycloalkyl-alkyl; aryl; arylalkyl; heteroaryl; heterocycloalkyl; or -COOH and/or -SO<sub>3</sub>H substituted alkyl; R<sup>1</sup>,R<sup>2</sup>,R<sup>3</sup>,R<sup>9</sup>, R<sup>10</sup> and R<sup>11</sup> are as defined in the specification; are disclosed, as well as pharmaceutical compositions containing them and a method of treating diseases associated with thrombosis, atherosclerosis, restenosis, hypertension, angina pectoris, arrhythmia, heart failure, and cancer by administering said compounds.

Full Text

BACKGROUND OF THE INVENTION Thrombin is known to have a variety of activities in different cell types and thrombin receptors are known to be present in such cell types as human platelets, vascular smooth muscle cells, endothelial cells and fibroblasts. It is therefore expected that thrombin receptor antagonists will be useful in the treatment of thrombotic, inflammatory, atherosclerotic and fibroproiiferative disorders, as.well as other disorders in which thrombin and its receptor play a pathological role. Thrombin receptor antagonist peptides have been identified based on structure-activity studies involving substitutions of amino acids on thrombin receptors. In Bernatowicz et al, J. Med. Chem., 39 (1996), p. 4879-4887, tetra- and pentapeptides are disclosed as being potent thrombin receptor antagonists, for example N-trans-cinnamoyl-p-fIuoroPhe-p-guanidinoPhe-Leu-Arg-NH2 and N-trans-cinnamoyl-p-fluoroPhe-p-guanidinoPhe-Leu-Arg-Arg-NH2. Peptide thrombin receptor anatgonists are also disclosed in WO 94/03479, published February 17, 1994. Cannabinoid receptors belong to the superfamily of G-protein coupled receptors. They are classified into the predominantly neuronal CB1 receptors and the predominantly peripheral CB2 receptors. These receptors exert their biological actions by modulating adenylate cyclase and Ca+2 and K+ currents. While the effects of CB1 receptors are principally associated with the central nervous system, CB2 receptors are believed to have peripheral effects related to bronchial constriction, immunomodulation and inflammation. As such, a selective CB2 receptor binding agent is expected to have therapeutic utility in the control of diseases associated with rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, diabetes, osteoporosis, renal ischemia, cerebral stroke, cerebral ischemia, nephritis, Inflammatory disorders of the lungs and gastrointestinal tract, and respiratory tract disorders such as reversible airway obstruction, chronic asthma and bronchitis (R. G. Pertwee. Gun-. Med, Chem. 6(8), (1999), 635). has been identified as a muscarinic receptor antagonist. The total synthesis of (+)-himbacine is disclosed in Chackalamannil et al, J, Am. Chem Soc. 118 (1996), p. 9812-9813. SUMMARY OF THE INVENTION The present invention relates to thrombin receptor antagonists represented by the formula 1 n is 1, 2, 3 or 4; n1 and n2 are independently 0-3, provided both are not 0; Het is a mono-, bi- or tricyclic heteroaromatic group of 5 to 14 atoms comprised of 1 to 13 carbon atoms and 1 to 4 heteroatoms independently selected from the group consisting of N, 0 and S, wherein a ring nitrogen can form an N-oxide or a quaternary group with a C1-C4 alky! group, wherein Het is attached to B by a carbon atom ring member, and wherein the Het group is substituted by 1 to 4 substituents, W, independently selected from the group consisting of R5, R10 and R11 are independently selected from the group consisting of R and This invention also relates to a method of using a compound of formula I in the treatment ofjhrcimbosis, atherosclerosis, restenosis, platelet aggregation, coagulation, cancer, inflammatory diseases or respiratory diseases, comprising administering a compound of formula I to a mammal in need of such treatment. In particular, the present invention relates to a method of using a compound of formula I in the treatment of thrombosis, atherosclerosis, restenosis, hypertension, angina pectoris, arrhythmia, heart failure, myocardial infarction, glomerulonephritis, thrombotic stroke, thromboembolytic stroke, peripheral vascular diseases, cerebral ischemia, cancer, rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, diabetes, osteoporosis, renal ischemia, cerebral stroke, nephritis, inflammatory disorders of the lungs and gastrointestinal tract, reversible airway obstnjction, chronic asthma or bronchitis. It is contemplated that a compound of this invention may be useful in simultaneously treating more than one of the diseases listed. In another aspect, the invention relates to a pharmaceutical composition comprising at least one compound of formula I in a pharmaceutically acceptable cam'er. In yet another aspect, the invention relates to the novel compounds represented by the structural formula DETAILED DESCRIPTION: The present invention relates to substituted tricyclic himbacine derivatives having one or more of anti-thrombotic, anti-platelet aggregation, antiatherosclerotic, antirestenotic and anti-coagulant activity. Thrombosis-related diseases treated by the compounds of this invention include thrombosis, atherosclerosis, restenosis, hypertension, angina pectoris, arrhythmia, heart failure, myocardial infarction, glomerulonephritis, thrombotic and thromboembolytic stroke, peripheral vascular diseases, other cardiovascular diseases, cerebral ischemia, inflammatory disorders, neurodegenerative diseases and cancer, as well as other disorders in which thrombin » and its receptor play a pathological role. Thrombin receptor antagonists are also known as protease activated receptor (PAR) antagQnists. The compounds of the invention also bind to cannabinoid (CB2) receptors and are useful in the treatment of inflammatory diseases or respiratory diseases such as one or more of rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis. diabetes, osteoporosis, renal ischemia, cerebral stroke, cerebral ischemia, nephritis. inflammatory disorders of the lungs and gastrointestinal tract, and respiratory tract disorders such as reversible airway obstruction, chronic asthma and bronchitis. Preferred definitions of the variables in the stnjcture of formula I are as follows: The sum of n1 and n2 is preferably 2-3, more preferably 3, Especially preferred are compounds of formula I wherein n1 is 1 and n2 is 2, or n1 is 0 and n2 is 3. "Alkenyl" means straight or branched carbon chains of 1 to 6 carbon atoms having one or more double bonds in the chain, conjugated or unconjugated. Similarly, "alkynyl" means straight or branched carbon chains of^ to 6 carbon atoms having one or more triple bonds in the chain. Where an alkyl, alkenyl or alkynyl chain joins two other variables and is therefore bivalent, the terms alkylene, alkenylene and alkynylene are used. Haloalkenyl means an alkenyl chain substituted by 1 to 3 halo atoms. "Cycloalky!" means a saturated carbon ring of 3 to 6 carbon atoms, while "cycloalkylene" refers to a con-esponding bivalent ring, wherein the points of attachment to other groups include all positional and stereoisomers. HalocycioalkyI means a cycioalkyi ring substituted by 1 to 3 halo atoms. "HeterocycloalkyI" as a substituent on Het means saturated rings of 4 to 7 atoms comprised of 3 to 4 carbon atoms and 1 to 3 heteroatoms selected from the group consisting of -0-, -S- and -NR^- joined to the rest of the molecule through a carbon atom. Examples of heterocyclo-alkyi groups are 2-azetidinyl, 2-pyrrolidinyl, tetrahydrothiophen-2-yl, tetrahydro-2-furanyl, 4-piperidinyl, 2-piperazinyI, tetrahydro-4-pyranyl, 2-morpholinyl and 2-thiomorpholinyl. "Halogen" refers to fluorine, chlorine, bromine or iodine radicals. When R4 and R5 join to fomn a ring with the nitrogen to which they are attached, the rings formed are 1-pyrrolidinyl, 1-piperidinyl and 1-piperazinyl, wherein the piperazinyl ring may also be substituted at the 4-position nitrogen by a group R^ "Dihydroxy(C1-C6)alkyl" refers to an alkyl chain substituted by two hydroxy groups on two different carbon atoms. "Aryl" means phenyl, naphthyl, indenyl, tetrahydronaphthyl or indanyl. "Heteroaryl" means a single ring, bicyclic or benzofused heteroaromatic group of 5 to 10 atoms comprised of 2 to 9 carbon atoms and 1 to 4 heteroatoms independently selected from the group consisting of N, O and S. provided that the rings do not include adjacent oxygen and/or sulfur atoms. N-oxides of the ring nitrogens are also included, as well as compounds wherein a ring nitrogen is substituted by a C1-C4 alkyl group to form a quaternary amine. Examples of single-ring heteroaryl groups are pyridyl, oxazolyl, isoxazolyl, oxadiazolyl, furanyl, pyrrolyl, thienyl, imidazolyl, pyrazolyl, tetrazolyl, thiazolyl, isothiazolyl, thiadiazolyl, pyrazinyl, pyrimidyl, pyridazinyl and triazolyl. Examples of bicyclic heteroaryl groups are naphthyridyl (e.g., 1, 5 or 1,7), imidazopyridyl, pyrido[2,3]imidazoiyl, pyridopyrimidinyl and 7-azaindolyl, Examples of benzofused heteroaryl groups are indolyl, quinolyl, isoquinolyl, phthalazinyl, benzothienyl (i.e., thionaphthenyi), benzimidazolyl, benzofuranyl, benzoxazolyl and benzofurazanyl. All positional isomers are contemplated, e.g., 1-pyridyl. 2-pyridyl, 3-pyridyl and 4-pyridyl. W-substituted heteroaryl refers to such groups wherein substitutable ring carbon atoms have a substituent as defined above, or where adjacent carbon atoms form a ring with an ' alkylene group or a methylenedioxy group. The term "Het" is exemplified by the single ring, bicyclic and benzofused heteroaryl groups as defined immediately above, as well as tricyclic groups such as benzoquinolinyl (e.g., 1,4 or 7,8)orphenanthrolinyl (e.g., 1,7; 1,10; or 4,7). Het groups are joined to group B by a carbon ring member, e.g., Het is 2-pyridyi. 3-pyridyl or 2-quinolyl. Examples of heteroaryl groups wherein adjacent carbon atoms form a ring with an alkylene group are 2,3-cyclopentenopyridine, 2,3-cyclohexenopyridine and 2,3-cycloheptenopyridine. glycine, valine, leucine, isoleucine, phenylalanine, trytophan, methionine, serine, theronine, cysteine, cystine, or tyrosine. The above statements, wherein, for example, R4 and R5 are said to be independently selected from a group of substituents, means that R4 and R5 are independently selected, but also that where an R4 or R5 variable occurs more than once in a molecule, those occurrences are independently selected. Those skilled in the art will recognize that the size and nature of the substituent(s) will affect the number of substituents which can be present. Compounds of the invention have at least one asymmetrical carbon atom and therefore all isomers, including diastereomers and rotational isomers are contemplated as being part of this invention. The invention includes (+)- and (-)-isomers in both pure form and in admixture, including racemic mixtures. Isomers can be prepared using conventional techniques, either by reacting optically pure or optically enriched starting materials or by separating isomers of a compound of formula I. Typical preferred compounds of the present invention have the following stereochemistry: with compounds having that absolute stereochemistry being more preferred. Those skilled in the art will appreciate that for some compounds of formula i, one isomer will show greater pharmacological activity than other isomers. Compounds of the invention with a basic group can form pharmaceutically acceptable salts with organic and inorganic acids. Examples of suitable acids for salt formation are hydrochloric, sulfuric, phosphoric, acetic, citric, oxalic, malonic. salicylic, malic, fumaric, succinic, ascorbic, maleic, methanesulfonic and other mineral and carboxyiic acids well known to those in the art. The salt is prepared by contacting the free base form with a sufficient amount of the desired acid to produce a salt. The free base form may be regenerated by treating the salt with a suitable dilute aqueous base solution such as dilute aqueous sodium bicarbonate. The free base form differs from its respective salt form somewhat in certain physical properties, such as solubility in polar solvents, but the salt is otherwise equivalent to its respective free base forms for purposes of the invention. Certain compounds of the invention are acidic (e.g., those compounds which possess a carboxyl group). These compounds form pharmaceutically acceptable salts with inorganic and organic bases. Examples of such salts are the sodium, potassium, calcium, aluminum, lithium, gold and silver salts. Also included are salts formed with pharmaceutically acceptable amines such as ammonia, alkyl amines, hydroxyalkylamines, N-methylglucamine and the like. ethyl, Me is methyl, Bn is benzyl, Ac is acetyl, AcOH is acetic acid, THF is tetrahydrofuran, DMF is dimethylformamide, rt is room temperature, Davis reagent is (1S)-(+H10-camphorsulfonyl)-oxaziridine, LHMDS is lithium bis(trimethylsilyl)amide, > 4-dimethylaminopyridine is DMAP, 1,8-cliazabicyclo[5.4.0]undec-7-ene is DBU, 1,3-dicyclohexylcarbodiimide is DCC. and trimethylsiiyi ipdide is TMSI. Compounds of formula l-A, wherein B is -CH=CH", Het is W-substituted pyridyl, R, R1, R3, R8, R9 R10 and R11 are each hydrogen. R2 is methyl, and R22 is -CO2Et can be prepared as shown in Scheme 1: The aldehyde 1 was converted to the dienoic acid 2 by a two step transformation. The acid was converted to its acid chloride using oxalyf chloride, which was then coupled with alcohol 3 to provide ester 4. The alkyne was selectively reduced to the cis-alkene 5, which upon thermal cyclization gave product 6. Debenzylation, followed by double bond reduction, gave the tricyclic acid 7. The acid was converi:ed to aldehyde I IB via its acid chloride, which was coupled with phosphonate III to provide l-A. In compounds of formula l-A, the ethylcarbamate group can be cleaved to provide the amine IA-1, which can be treated with a wide range of electrophiles such as acid chlorides, suifonyl chlorides, isocyanates. chloroformates etc. to provide amides, sulfonamides, ureas and carbamates etc. as shown in Scheme 2. The aldehyde of formula IIB can also be coupled with phosphonate 8 to provide NA3, which can be transformed into carbamate I-A4 as shown in Scheme 3. Both I-A3 and I-A4 can be converted into diverse analogs using methodologies such as Suzuki coupling, Stille coupling, Buchwald amination etc (Scheme 4). The arylbromide I-A3 can also be converted to aniline I-A5, which can be treated with many readily accessible electrophiles such as acid chlorides, sulfonamides, isocyanates etc. to provide the corresponding derivatives I-A6 as shown in Scheme 5. The α-position of the lactone portion can be functionalized, for example compounds of formula l-A wherein R1 is hydrogen can be converted to the corresponding compounds wherein R1 is OH by treatment with Davis reagent ((1S)-(+)-(10-camphorsulfonyl)-oxaziridine) and LHMDS. Similar processes known to those skilled in the art can be used to prepare compounds comprising other optionally substituted Het groups and other "R" variables. Those skilled in the art will also recognize that the processes are equally applicable to preparing optically active or racemic compounds. Compounds of formula I wherein R1 is hydrogen can be converted to the corresponding compound wherein R® is hydroxy by heating with an oxidizing agent such as SeO2. Phosphonates of formula III wherein W is aryl or R21-aryl can be prepared by a process similar to that described immediately below for preparing the trifluoromethyl-phenyl-substituted compound, Ilia. Commercially available hydroxypyridine derivative is converted to the corresponding triflate using triflic anhydride, which is then coupled with commercially available boronic acid in the presence of Pd(0) under Suzuki conditions. The resulting product is converted to the phosphonate by treatment with n-butyllithium followed by quenching with diethylchlorophosphate. starting materials for the above processes are either commercially available, known in the art, or prepared by procedures well known in the art. Reactive groups not involved in the above processes can be protected during the reactions with conventional protecting groups which can be removed by standard procedures after the reaction. The following Table A shows some typical protecting groups: To a solution of 5.6-dihydro-2H-pyridine-1,3-dicarboxylic acid 1-ethyl ester 3-methyl ester (35.4 g. 166 mmol) in CH2CI2 (600 ml) at -78 °C was slowly added a solution of 1M DIBAL (365 ml, 365 mmol, 2.2 eq.) in CH2CI2, and the mixture stirred for 1.5 hr. The reaction was quenched by the addition of 1 liter of saturated aq. Rochelle's salt and the organic layer was separated. The aqueous layer was extracted with 2x250 ml of CH2CI2 and the combined organic layer was washed with 500 ml brine, dried over MgSO4, filtered, concentrated and the resultant crude was chromatographed with 40% EtOAc-hex to provide 17 g (55%) of alcohol as an oil. To a solution of above alcohol (17.0 g, 92 mmol) in 150 ml of CH2CI2 at rt was added NaHCOs (15.4 g, 183 mmol. 2 eq.) and Dess-Martin reagent (46.7 g, 110 mmol, 1.2 eq.) and the suspension was stirred for 45 min. To this was added 300 ml of EtsO and a solution of Na2S203.5H20 (70 g, 282 mmol. 2 eq.) and NaHCOs (1.5,4 g. 183 mmol, 2 eq.) in 600 ml H2O. The mixture was stirred vigorously until the two layers became clear. The organic layer was separated and the aqueous layer was extracted with 2x150 ml of Et20. The combined organic layer was washed with 300 ml each of aq. Na2S2O3/NaHCO3 and brine, dried over MgSO4, filtered and evaporated to give 15.3 g (91%) of oil. HRMS: 184.0966 (MH"). To a suspension of 60% NaH (4.35 g. 109 mmol, 1.3 eq.) in THF (300 ml)at 0 °C was added dropwise triethyl phosphonoacetate (20 ml, 109 mmol. 1.3 eq) and the mixture was stinted at 0 °C for 30 min. To this was added a solution of the product of Step 1 (15.3 g, 83.5 mmol) and the mixture was stirred for 30 min. at 0 "^C. The reaction was quenched by the addition of 600 ml of aq. NH4CI, the THF was evaporated and the aqueous slurry was extracted with 3x200 mNof Et2O. The combined organic layer was washed with 200 ml of brine, dried over MgSO4, filtered, concentrated and chromatographed with 15% EtOAc-hex to provide 19.9 g (94%) of oil. MS:254(MH+) To a solution of the product of Step 2 (19.9 g, 79 mmol) in 100 ml each of CH3OH. THF and HgO was added KOH (13.3 g, 237 mmol, 3 eq.) and the mixture was stin-ed at rt for 2 h. The mixture was diluted with 200 ml of H2O, acidified with 1N HCI to -pH 2 and extracted with 3x200 ml of EtOAc. The combined organic layer was washed with 200 ml each of H2O and brine, dried over MgSO4, filtered and evaporated to give 17.0 g (96%) of pale-yellow solid, HRMS: 226.1083 (MH") To a solution of dienoic acid (17.0 g, 76 mmol) in 400 ml CH2CI2 at rt was added oxalyl chloride (13.2 ml, 151 mmol. 2 eq.) and DMF (120 |al, 1.6 mmol, 2 mol%). The mixture was stirred for 1 h, concentrated and evaporated with 100 ml anhydrous toluene to provide the acid chloride. To a solution of the above acid chloride in 200 ml CH2CI2 at 0 °C was added DMAP (925 mg, 7.6 mmol, 0.1 eq.), a solution of the product of Step 3 (15.4 g, 75 mmol, 1.0 eq.) in 15 mi CH2CI2 followed by Et3N (12.7 ml, 91 mmol, 1.2 eq.). The mixture was stirred for 1.5 hr at 0 °C, then diluted with 600 ml of Et2O. The solution was washed successively with 200 ml H2O, 2x200 ml 1N HCI, 200 ml aq. NaHCOj and 200 ml brine. It was dried over anhydrous MgSO4, filtered, concentrated and chromatographed with 20% EtOAc-hex to provide 20 g (78%) of resin. HRMS: 412.1764 (MH+). A suspension of the product of Step 4 (10 g, 29 mmol), quinoline (700 μ1, 5.9 mmol, 0.2 eq.) and Lindlar catalyst (1.0 g, 10 wt%) in 150 ml THF was stirred under 1 atm. H2 for 2.5 h. Another batch of 10 g of the product of Step 4 was similarly reduced with Lindlar catalyst. The batches were combined, filtered through ceiite, evaporated and the residue was re-dissolved in 600 ml EtOAc. It was washed with 3x200 ml of 1N HCl and 200 ml of brine, dried over MgSO4, filtered and evaporated to give 20 g of resin which was used immediately for the Diels-Alder reaction in Step 6. HRMS: 414.1919 (MH+). A solution of the product of Step 5 (20.0 g) in 500 ml toluene was heated in a pressure vessel at 185 °C for 6 h. It was cooled to rt, treated with DBU (1.8 ml, 12 mmol, 0.2 eq.) for 1 h, concentrated and chromatographed with 25% EtOAc-hex to provide 11.3 g (56%) of the cyclized exo product. HRMS: 414.1923 (MH*). A suspension of the product of Step 6 (11.2 g, 27 mmol), 10% Pd-C (1.2 g, 10 wt%) in 200 ml EtOAc was stirred under 1 atm. H2 until the reaction was complete. It was filtered through celite, concentrated and re-dissolved in 200 ml of CH3OH. To this was added 900 mg of PtO2 and the suspension was shaken under 50 atm. of H2 in a parr vessel. The mixture was filtered through celite and concentrated to provide 8.5 g of resin. HRMS: 326.100 (MH*). Step 8: To a solution of the product of Step 7 (415 mg, 1.28 mmol) in 10 ml CH2Cl2 at 1 was added oxalyl chloride (225 \i\, 2.58 mmol, 2 eq.) followed by 1 drop of DMF. The solution was stirred at rt for 1 h, at which time there was no evolution of gas. It /vas concentrated and azeotroped with anhydrous toluene to give the acid chloride. The acid chloride was dissolved in 6 ml of anhydrous toluene, cooled to 0 °C and ='d(PPh3)4 (74 mg, 0.064 mmol, 5 mol%) was added, followed by BUgSnH (520 ^1, 1.93 mmol, 1.5 eq.). The mixture was stirred at 0 °C for 3 hr, concentrated and Dhromatographed with 50% EtOAc-hex to provide 360 mg (91%) of the title compound as a resin. MS: 310.1 (MH+). 3-Formyl"5,6-ciihydro-2H-pyran was converted to the tricyclic aldehyde using similar procedure described above for the corresponding amine analogs. To a solution of the phosphonate (3.49 g, 11,3 mmol, 2 eq.) in THF (50 ml) at 0 °C was added a 1M solution of LHMDS in THF (11.3 ml, 11.3 mmol, 2eq.). After stirring for 10 min., Ti(O)4 (3.4 ml, 11.3 mmol, 2 eq.) was added, followed by a solution of Preparation 1 (1.75 g, 5.7 mmol, 1 eq.) in THF (10 ml), and the mixture was stirred for 1 h under N2. The reaction mixture was poured into 5% aqueous tartaric acid solution (100 ml) and extracted with EtOAc (3x100 n:^l). The combined organic layers were washed with brine (150 ml), dried with MgSO4, filtered and evaporated to dryness. Purification by silica gel chromatography eluting with 5% CH3OH - CH2CI2 yielded 1,80 g (70%) of the title compound as a pale yellow foam. 1H NMR (400 MHz, CDCI3): 8.59 (d, J = 4.8Hz, 1H), 7.76 (dd, J = 3Hz, 8.4Hz, 1H), 7.06 (d, J = 8.4Hz, 1H), 6.56 (dd, J = 9.6Hz, 15.2Hz, 1H), 6.45 (d, J = 15.2Hz, 1H), 4.73 (m, 1H), 4.35-4.05 (m, 2H), 4.12 (q. J = 6.8Hz, 2H), 2.73-2.69 (m, 2H), 2.47- 2,35(m. 3H). 1.96 (q, 6.0Hz. 1H). 1.74 (d, J = 12.8Hz, 1H), 1.41 (d. J = 6.0Hz, 3H), 1.35-1.18 (m, 7H), 1.10^ 0.98 (m. 1H).. To a solution of Preparation 3 (0.270 g, 0.58 mmol) in CH2CL2 (15 ml) was added TMSI (624μl, 4.4 mmol, 7.5 eq.), and the mixture was heated to reflux. After 6 h, the mixture was poured onto aqueous NaHCOg (30 ml) and extracted with CH2CL2 (3x15 ml). The combined organic layers were washed with brine, dried with MgSO4, filtered and evaporated to dryness resulting in 209 mg of amine (92%). To the above product in CH2CL2 (15 ml) at 0 °C was added Et3N (97 μl. 0.69 mmol, 1.3 eq.) and chloroformic acid 2-methoxyethyI ester (68 I, 5.9 mmol, 1.1 eq.); the mixture was allowed to slowly warm to rt while stirring under N2. After 1 h, the mixture was poured onto water (30 ml) and extracted with CH2CL2 (3x15 ml). The combined organic layers were washed with brine (30 mi), dried with MgSO4, filtered and evaporated to dryness. Purification by silica gel chromatography, eluting with 3% CH3OH - CH2CL2, yielded 183 mg of the title compound as a white solid (69%). 'H NMR (400 MHz, CDCI3): 8.59 (d, J = 2.4Hz. 1H), 7.76 (dd, J = 2.4, 8.2Hz, 1H). 7.06 (d, J = 8,3Hz, 1H) 6.56 (dd, J = 9.6, 15.4Hz, IN), 6.45 (d, J = 15.4Hz, 1H), 4.72 (m, 1H), 4.1-4.28 (m. 4H). 3.59 (t. J = 4.49Hz, 2H), 3.38 (s, 3H), 2.75-2.68 (m, 2H), 2.32-2.51 (m, 3H), 1.96 (dd, J = 6.3,12,8Hz, 1H), 1.73 (d, J = 12.5Hz, 1H), 1.41 (d, J = 5.95Hz. 3H), 1.37-1.00 (m. 4H). The thiopyran enal was prepared according to the procedure of McGinnis and Robinson, J. Chem. Soc, 404 (1941), 407. Step 2: To a suspension of 60% NaH (6.3 g, 158 mmol, 1.3 eq.) in THF (200 nn() at 0°C was added methyl diethylphosphonoacetate (29 ml, 158 mmol, 1.3 eq.) and the mixture was stirred at 0°C for 30 min. The solution was then transferred to a solution of the product of Step 1 (15.6 g, 122 mmol) in THF (100 ml) and stirred at 0°C for 1 h. The reaction was quenched by the addition of aq. NH4CI (500 ml) and the THF was evaporated. The aqueous phase was extracted with Et20 (3x200 ml) and the combined organic layer was washed with H2O and brine (200 ml each). The solution was dried over MgSO4, concentrated and the resultant residue was chromatographed with 5% EtOAc-hexane to provide 13.0 g (58%) of oil. 1H NMR (400 MHz, CDCy 7.26 (d, J = 15.9 Hz, 1H), 6.26 (t, J =4.4 Hz, 1H), 5.78 (dd, J = 15.9, 0.6 Hz, 1H), 3.75 (s, 3H), 3.25-3.23 (m, 2H), 2.71 (t, J = 5.8 Hz, 2H), 2.57-2.53 (m, 2H). To a solution of the product of Step 2 (13.0 g, 70.6 mmol) in THF and MeOH (50 ml each) was added a solution of KOH (11.9 g, 212 mmol, 3.0 eq.) in H2O (50 ml). The mixture was stirred at rt for 1 h, diluted with HjO (100 ml) and acidified with IN HCI. The aqueous phase was extracted with EtOAc (3x200 ml) ahd the combined organic layer was washed with H2O and brine (300 ml each). The solution was dried over MgSO4, filtered and evaporated to give 11.66 g (97%) of pale-yellow solid. ^H NMR (400 MHz, CDCl3) 7.34 (d, J = 15.6 Hz, 1H), 6.32 (t, J = 4.4 Hz, IN), 5.78 (d, J = 15.6 Hz, 1H), 3.26 (d, J = 1.6 Hz, 2H), 2.72 (t, J = 5.8 Hz, 2H), 2.59-2.55 (m, 2H). To a solution of 4 (5.2 g) in EtOAc (120 ml) was added Lindlar catalyst (520 mg) and the suspension was stirred under 1 atm. H2. Another portion of catalyst (500 mg) was added after 45 min. and the mixture stirred for further 30 min. The mixture was filtered through a celite pad and evaporated to provide 5.2 g (99%) of the desired alkene. 'H NMR (400 MHz, CDCI3) 7.38-7.26 (m, 5H), 6.32 (dd, J = 11.9, 6.6 Hz. 1H), 5.86 (d, J = 12.0 Hz, 1H), 5.18 (s, 2H), 5.12-5.07 (m, 1H), 3.20 (br s, 1H), 1.34 (d, J = 6.6 Hz, 3H). To a solution of the product of Step 3 (2.45 g, 14.39 mmol) in CH2CL2 (60 ml) at 0°C was added DCC (3.27 g, 15.85 mmol, 1.1 eq.) followed by DMAP (352 mg, 2.88 mmol, 0.2 eq.) and the mixture was stirred at 0°C for 30 min. To this was added a solution of 3.27 g (15.85 mmol, 1,1 eq.) of the alcohol of Step 4 in 10 ml of CH2CL2 and the mixture was stirred at 0 °C for 5 hr and at rt for 1 hr. The solution was diluted with 350 miof Et20 and washed with 2x200 ml of aq. citric acid, 200 ml of aq. NaHCOg and 200 ml of brine. The solution was dried over MgSO4, filtered, concentrated and the resultant residue was chromatographed with 6% EtOAc-hex to provide 2.1 g (41%) of resin. 'H NMR (400 MHz, CDCI3) 7.38-7.32 (m, 5H), 7.45 (d, J = 16.0 Hz, 1H), 6.38-6.34 (m, 1H), 6.26 (t, J = 4.6 Hz, 1H), 6.21 (d, J = 11.6 Hz, 1H), 6.19 (d, J = 11.2 Hz, 1H), 5.85 (dd, J = 11.6, 1.2 Hz, 1H), 5.76 (d, J = 16.0 Hz, 1H), 5.18 (d, J = 1.2 Hz, 2H), 3.24 (d, J = 2.0 Hz, 2H), 2.71 (t, 2H, J = 5.6 Hz, 2H)> 2.56-2.52 (m, 2H), 1.41 (d, J = 6.4 Hz, 3H) A solution of the product of Step 5 (2.1 g, 5.85 mmol) in m-xylene (50 ml) was heated at 200°C for 6 h in sealed tube. The solution was cooled to rt and stirred with DBU (178 I, 1.19 mmol, 0.2 eq.) for 1 h, concentrated and chromatographed with 15% EtOAc-hexane to provide 1.44 g (69%) of the desired exo product. '1H NMR (400 MHz, CDCy 7.39-7.35 (m, 5H). 5.46 (br s, 1H), 5.16 (ABq, J = 21.6, 12.0 Hz, 2H), 4.42 (dq, J = 9.2, 6.0 Hz, 1H), 3.36-3.33 (m 2H), 3.08 (dd, J = 14.4, 2.4 Hz, 1H), 2.85 (ddd, J = 13.9, 12.4, 2.5 Hz, 1H), 2.72-2.57 (m, 4H), 2.27-2.21 (m, 1H), 1.47-1.25 (m, 1H), 1.12 (d, J = 6.4 Hz, 3H) To a solution of the product of Step 6 (750 mg, 2.09 mmol) in CH2CL2 (10 ml) at -78°C was added BBrg in CH2Cl2 (4.2 ml of 1M solution). The solution was stirred at -78X for 30 min. and at 0 °C for 30 min, then poured into aq. K2CO3 (100 ml). The aqueous phase washed with Et2O (2x50 ml) and the organic layer was back extracted with aq. K2CO3 (50 ml). The combined aqueous phase was acidified with IN HCI and extracted with EtOAc (3x50 ml). The EtOAc layer was washed with brine (50 mi), dried over MgSO4, filtered and evaporated to provide 500 mg (89%) of acid. 'H NiVlR (400 MHz, CDCI3) 5.50 (br s, 1H), 4.47 (dq, J = 9.6, 6.0 Hz, 1H), 3.43-3.39 (m, 1H), 3.36 (d, J = 15.6 Hz, 1H), 3.10 (dd, J= 14.0, 2.4 Hz, 1H), 2.91-2.84 (m, 1H), 2.82-2.77 (m, 1H), 2.70 (dd, J = 10.6, 4.2 Hz, 1H), 2.69-2.63 (m, 1H), 2.57-2.52 (m, 1H), 2.34-2.29 (m, 1H), 1.53-1.42 (m, 1H), 1.34 (d, J = 6.0 Hz, 3H). To a solution of the product of Step 7 (500 mg, 1.86 mmol) in MeOH (30 ml) was added AcOH (3 ml) and PtO2 (250 mg) and the suspension was shaken under 40 Psi H2 in a Parr vessel for 1.5 days. The catalyst was filtered off with a celite pad, the solution was concentrated and the resultant residue was dissolved in AcOH-MeOH-, CH2CL2 mixture (0.5:2:97.5 v/v/v/) and filtered through a short SiO2 column to provide 400 mg (79%) of the reduced product as a resin which solidified on standing. 1H NMR (400 MHz, CDCI3) 4.68 (dq, J = 9.4, 5.9 Hz, 1H), 2.76-2.69 (m, 2H), 2.60-2.55 (m, 3H), 2.49 (d, J = 11.6 Hz, 1H), 2.10 (br s, 1H), 1.93 (ddd, J = 13.5, 6.0, 2.7 Hz, 1H), 1.60-1.48 (m, 2H), 1.45-1.19 (m, 3H), 1.33 (d, J = 5.6 Hz, 3H). Step 9: To a solution of the product of Step 8 (97 mg, 0.36 mmol) in CH2Clg (4 ml) was added oxalyl chloride (94 μl) followed by 1 drop of DMF. The solution was stirred for 1 h at rt and concentrated to provide the cmde acid chloride which was dissolved in toluene (3 ml) and cooled to 0°C. Pd(PPh3)4 (42 mg, 0.04 mmol, 0.1 eq.) was added, followed by BUgSnH (94 ^1), The mixture was stirred at 0° C for 3 h, concentrated and chromatographed with 25% EtOAc-hexane to provide 73 mg (80%) of aldehyde as white solid. 1H NMR (400 MHz, CDCI3) 9.75 (d, J = 2.8 Hz, 1H), 4.62 (dq, J = 9.7, 6.0 Hz, 1H), 2.8-2.70 (m, 2H), 2.65-2.55 (m, 3H), 2.50 (d, J = 7.2 Hz), 2.10 (ddd, J = 13.2, 6.4, 3.0 Hz, 1H), 1.94 (ddd, J = 13.6, 6.0, 3.0, 1H), 1.69 (dq, J = 10.9 Hz, 3.00 Hz, 1H), 1.58-1.48 (m, 1H), 1.42-1.20 (m, 3H), 1.33(d, J = 6.4 Hz. 3H). 5-Valerolactam was dissolved in THF (250 ml) and cooled to -78°C. n-BuLi (28.44 ml, 1.1 eq, 2.5 M solution in hexanes) was added dropwise. The mixture was stirred for 30 min, then ethyl chloroformate (6.49 mi; 1.05 eq) was added and the mixture allowed to warm to rt. Water was added and the organic layer extracted with EtOAc. The combined organic layers were dried and concentrated to give 11.57 g of oil. 1H NMR (400 MHz, CDCl3) 4.29 (2 H, q, J=7.2 Hz), 3.71 (2 H, br t, J=5.6 Hz), 2.50 (2 H, brt, J=6.8 Hz), 1.83 (4 H, brs), 1.33 (3 H, t, J=7.2 Hz). The product of step 1 was dissolved in THF (250 ml) and the solution cooled to -78°C. LHMDS (65 ml, 1 eq, 1 M solution in THF) was added dropwise and the resulting mixture stirred for 30 min. A solution of 2-[N,N-bis(trifluoromethylsulfonyl)-amino]-5-chloropyridine in THF (73 ml) was added dropwise. The resulting mixture was stirred for 10 min and allowed to warm to rt. Water was added and the organic layer extracted with EtOAc. The combined organic layers were dried and concentrated. Chromatography (5-10 % EtOAc in Hexane) gave 12.0 g of oil, 'H NMR (400 MHz, CDCl3 5.32 (1 H, t, J=3.6 Hz), 4,24 (2 H, q, J= 7.2 Hz), 3.66 (2 H, m). 2,27 (2H, m). 1.78 (2 H, m), 1.30 (3H, J=7.2 Hz), Borane dimethylsulfide complex (5.82 ml. 1.05 eq) was dissolved in THF and cooled to 0°C. (1R)-(+)-α-pinene (22.56 ml, 2.32 eq) was added dropwise, the mixture was stirred at O^^C for 1 h and at rt for 2 h. The mixture was cooled to -35°C and ethyl propiolate (6.2 ml, 1 eq) was added dropwise; the mixture was stirred at "35°C for 45 min and rt for 3 h. Acetaldehyde (48 ml) was added and the mixture heated at 40-41 °C overnight. The volatile organic components were carefully removed under reduced pressure to give 29g of a mixture of the product and α-pinene (1:2.3 by NMR). 1H NMR (400 MHz, CDCI3) characteristic peaks for the product include, 6.95 (1 H, d, J=18.0 Hz), 6.48 (1 H, d, J=18.0 Hz). 4.12 (2 H, q, J=7.2 Hz), 3.60 (4 H, q, J=7.2 Hz), Pd(0Ac)2 (592 mg, 10 %) and 2-(di+butylphosphino)biphenyl (1.57 g, 20 %) were dissolved in THF (100 ml). The mixture was stirred for 10 min under N2, then a mixture of the product from step 2 (8 g) and the product from step 3 (20 g. 1.5 eq) in THF (32 ml) were added. KF (4.6 g) was then added and the mixture heated at 55°C overnight. The mixture was allowed to cool to rt and diluted with EtOAc. The mixture was washed with NaHCO3(sat), NH4CI(sat), water, and finally dried over MgSO4. Removal of solvents under reduced pressure followed by column chromatography (10% EtOAc in hexane) gave 6g (89%) of a colorless oil. 1H NMR (400 MHz, CDCI3) 7.21 (1 H, d, J=15.6 Hz), 5.88 (1 H, d, J=15.6 Hz), 5.69 (1 H, t, J=4.0 Hz), 4.15 (4 H, m), 3.59 (2 H, m). 2.26 (2H, m), 1.82 (2H, m), 1.25 (6 H, m). Step 5: The product from step 4 was dissolved in a 1:1 mixture of MeOH and THF (66 ml). A solution of 1N NaOH (52 ml) was added and the mixture stirred for 2.5 h until no starting material remained. The mixture was acidified to pH1 with 2 N HCI and extracted with EtOAc. The extracts were washed with NH4CI (sat), dried, and concentrated under reduced pressure to give 5 g of a solid. ^H NMR (400 MHz, CDCI3) 7.30 (1 H, d, J=15.2 Hz), 5.87 (1 H, d, J=15.2 Hz), 5.73 (1 H, m), 4.14 (2H, m), 3.60 (2 H, m), 2.70 (2 H, m), 1.82(2H, m), 1.23(3H, m). To a solution of phosphonate (156 mg, 0.42 mmol, 2.0 eq.) in THF (1 ml) at 0 °C was added a 2.5 M solution of BuLi in hexanes (170 μl, 0.42 mmol, 2.0 eq.) and the mixture was stirred for 30 min. To this was added a solution of Preparation 5 (53 m, 0.21 mmol) in THF (1.5 ml) and the mixture was stirred at 0 °C for 1 h. The reaction was quenched by the addition of aq. NH4CI (20 ml), the THF was evaporated and the aqueous phase was extracted with CH2CL2 (3x10 ml). The combined organic layer was washed with aq. NaHCOg (15 ml) and brine (15 ml), dried over MgSO4, filtered, concentrated and chromatographed with 40% EtOAc-hex to provide 90 mg (91%) of resin. HRMS: 474.1721. The thiopyran compound of Example 1 can be converted to the corresponding sulfoxide (1 A) and sulfone (1B) by the following procedure: To a solution of Example 1A (70 mg, 0.15 mmol) in AcOH (2 ml) was added CH3SO3H (50μl 5 eq.) and NaBO3.4H20 (30 mg, 0.19 mmol, 1.3 eq.), and the . mixture was stirred overnight at rt. The acetic acid was evaporated and the resultant residue was taken in aq. NaHCO3-Na2SO3 mixture (25 ml) and extracted with CH2CL2 (3x15 ml). The combined organic layer was washed with brine (20 ml), dried over MgSO4, filtered, concentrated and purified by preparative thin layer chromatography to provide 11 mg of sulfoxide isomer 1, 4 mg of sulfoxide isomer 2, and 36 mg of sulfone. Sulfoxide isomer 1: HRMS: 490.1661 (MH+); Sulfoxide isomer 2: 1H NMR (400 MHz, CDCI3): 8.80 (d, J = 2.4 Hz, 1H), 7.87 (dd, J = 8.0, 2.0 Hz, 1H), 7.81 (s, 1H), 7.76 (d, J = 7.6 Hz, 1H), 7.67 (d, J = 7.6 Hz, 1H), 7.61 (t, J = 7.8 Hz, 1H), 7.27 (d, J = 9.6 Hz, 1H), 6.67-6.55 (m, 2H), 4.78-4.71 (m, 1H). 3.44-3.40 (m, 1H), 3.35 (dt, J = 12.1, 2.8 Hz, 1H), 2.78-2.71 (m, 1H), 2.64-2.57 (m, 1H), 2.52-2.36 (m, 3H), 2.26-2.21 (m, 1H), 2.04 (ddd, J = 13.5, 6.5, 2.7 Hz, 1H), 1.45 (d, J = 6.0 Hz, 3H), 1.60-1.25 (m, 6H) Sulfone: HRMS: 506.1612 (MH+). To a solution of phosphonate (2 eq) in THF at 0 °C is added 2.5M BuLi in hexanes (2.0 eq.). After stim'ng for about 2 h, Ti(0'Pr)4 (2.0 eq) is added, followed by a solution of aldehyde in THF (1.0 eq.). The mixture is stirred at rt for 30 min, diluted with aq. sodium potassium tartrate and extracted with EtOAc. The combined organic layer is washed with brine, dried over MgSO4, filtered, concentrated and purified by column chromatography to provide the product. To a solution of Example 2D (380 mg, 0,79 mmol) in THF (7 ml) at -78 °C was added 1M solution of LHMDS in THF (0.95 ml, 0.95 mmol, 1.2 eq.); the mixture was stirred for 30 min at -78 °C, 30 min at 0 °C, then cooled back to -78 °C. To this was added a solution of (1SH+H10-camphorsulfonyl)oxazJridine (275 mg, 1.1 mmol, 1.5 eq.) in THF (2 ml). The solution was stin-ed ovemight while allowing to warm up to rt. It was diluted with aq. NH4CI (100 ml), the THF was evaporated and the aqueous phase extracted with EtOAc (3x30 ml). The combined organic layer was washed with brine (30 ml), dried over MgSO4, filtered, concentrated and chromatographed with 2%CH30H-CH2Cl2 to provide 94 mg of resin. HRMS: 495.2291 (MH") Example 4 V V A solution of carbamate and trimethylsilyl iodide (5 eq.) was refluxed for about 5 hr then diluted with aq, NaHCOg. The aqueous layer was extrated with CH2CL2 and the combined organic layers was washed with brine, dried over MgSO4, filtered and concentrated to give the amine. A solution of the amine from above in CH2CL2 was treated with Et3N (5 eq.) and acid chloride (3 eq) and the reaction was followed by thin layer chromatography. After the reaction was completed, it was subjected to standard aqueous work-up and the crude product was purified by preparative thin layer chromatography or column chromatography to afford the amide. The amine can similariy be treated with many electrophiles such as-sulfonylchlorides, isocyanates, chloroformates and aldehydes etc. to provide the appropriate derivatives. Compounds of the following formula were prepared by this route: wherein W and R22 are as defined in the table: General procedure: A solution of a product of Preparation 3 or 4 and W-B(OH)2, wherein W is optionally substituted phenyl or heteroaryl, K2CO3 (4 eq.) and Pd(PPh3)4 (5 to 10 mol%) in PhMe-EtOH-HjO (4:2:1 v/v/v) was heated at 100 °C until the reaction was complete. The reaction mixture was diluted with H2O. extracted with EtOAc, the organic layer was washed with brine, dried over MgSO4, filtered, concentrated and purified by chromatography to provide the desired compounds. The compounds can be further derivatized. Using this method, compounds of the following formula were prepared To a solution of Preparation 3 (100 mg, 0.22 mmol) in toluene (5 ml) was added Pd(OAc)2 (5 mg, 0.022 mmol, 0.1 eq.), (S)-(-)-2,2'-bis{dlphenylphoshphino)-1,1'-binaphthyl (13 mg, 0.022 mmol, 0.1 eq.) and 2-tributylstannyl pyridine (119 mg, 0.32 mmol, 1.5 eq.). The mixture was bubbled with N2 for 5 min., then heated to 100 °C in a pressure tube. After 16 h, the mixture was poured onto aqueous NH4CI (15 mi), and extracted with EtOAc (3x15 ml). The combined organic layers were washed with brine, dried with MgSO4, filtered and evaporated to dryness. Purification by silica gel chromatography, eluting with 2% CH3OH - CH2CL2, followed by silica gel chromatography eluting with 60% EtOAc-hex, yielded 30 mg (30%) of product. HRMS: 462.2401 (MH") To a solution of Preparation 3 (100 mg, 0.22 mmol) in dry toluene (5 ml) was added pyrrolidine (36 μl, 0.43 mmol, 2 eq.), potassium phosphate (137 mg, 0.65 mmol, 5 eq.), Pd(OAc)2 (3 mg, 0.014 mmol, 0.065 eq.), and 2-(dicyclohexyl-phosphino)biphenyl (10 mg, 0.028 mmol, 0.13 eq.). The mixture was bubbled with N2 for 5 min., then heated to 100 "C in a pressure tube. After 16 h, the mixture was poured onto water (15 ml) and extracted with EtOAc (3x15 ml). The combined organic layers were washed with brine (15 ml), dried with MgSO4, filtered and evaporated to dryness. Purification by preparative thin layer chromatography, eluting with 5% CH3OH - CH2CL2, yielded 10 mg of solid HRMS: 454.26^6 (MH^) Using a similar procedure, the following compound was prepared: To a solution of Preparation 3 (1.0 g, 2.18 mmol) in ethylene glycol dimethyl ether (25 ml) was added benzophenone imine (550 jj.!, 3.27 mmol, 1.5eq.), potassium phosphate (1.51 g, 6.6 mmol, 3 eq.), tris(dibenzy(ideneacetone)dipalladium(0) (200 mg, 0.22 mmol, 0.1 eq.) and 2-(dicyclohexylphosphino)biphenyl (153 mg, 0.44 mmol, 0.2 eq.). The mixture was bubbled with N2 for 5 min., then heated to 100 °C in a pressure tube for 4 h. The mixture was then filtered through celite and evaporated to dryness. To this residue in CH2CL2 (25 ml) was added concentrated aqueous HCI (545 ^L, 6.6 mmol, 3 eq.) and the mixture was stirred at rt. After 16 h, the mixture was diluted with CH2CL2 (25 ml), poured onto aqueous 1N NaOH (50 ml) and extracted with CH2CL2 (3x50 ml). The combined organic layers were washed with brine, dried with MgSO4, filtered and evaporated to dryness. Purification by silica gel chromatography, eluting with 2% CH3OH-CH2CL2 yielded 550 mg^63%) of the title compound, MS: 400 (MH+) The compound of Example 8 was treated with electrophiles such as acid chlorides, suifonyi chlorides, isocyanates etc. to provide the following compounds. Example 9 Using the product of Preparation 6 and the general procedures of Preparation 1, Preparation 3 and Example 5, compounds of the following structure were prepared at least one compound of formula I of this invention and a phamiaceutically acceptable carrier. Preferably, one or two compounds of formula I are present in the composition, more preferably one compound of formula i. The compounds of formulal can be administered in any conventional oral dosage form such as capsules, tablets, powders, cachets, suspensions or solutions. The formulations and pharmaceutical compositions can be prepared using conventional pharmaceuticaliy acceptable excipients and additives and conventional techniques. Such pharmaceuticaliy acceptable excipients and additives include noji-toxic compatible fillers, binders, disintegrants, buffers, preservatives, anti-oxidants, lubricants, flavorings, thickeners, coloring agents, emulsifiers and the like. The daily dose of a compound of formulal for treatment of a disease or condition cited above is about 0.001 to about 100 mg/kg of body weight per day, preferably about 0.001 to about 10 mg/kg. For an average body weight of 70 kg, the dosage level is therefore from about 0.1 to about 700 mg of drug per day, given in a single dose or 2-4 divided doses. The exact dose, however, is determined by the attending clinician and is dependent on the potency of the compound administered, the age, weight, condition and response of the patient. The following fonnulations exemplify some of the dosage forms of this invention. In each, the term "active compound" designates a compound of formula I. Mix Item Nos. 1 and 2 in suitable mixer for 10-15 minutes. Granulate the mixture with Item No. 3. Mill the damp granules through a coarse screen (e.g., 1/4", 0.63 cm) if necessary. Dry the damp granules. Screen the dried granules if necessary and mix with Item No. 4 and mix for 10-15 minutes. Add Item No. 5 and mix for 1-3 minutes. Compress the mixture to appropriate size and weight on a suitable tablet machine. Method of Manufacture MIX Item Nos. 1, 2 and 3 in a suitable blender for 10-15 minutes. Add item No. 4 and mix for 1-3 minutes. Fill the mixture into suitable two-piece hard gelatin capsules on a suitable encapsulating machine. The activity of the compounds of formula I can be determined by the following procedures. In Vitro Testing Procedure for Thrombin Receptor Antagonists: Preparation of [3H]haTRAP A(pF-F)R(ChA)(hR)(l2-Y)-NH2 (1.O3 mg) and 10% Pd/C (5.07 mg) were suspended in DMF (250 pi) and diisopropylethylamine (10 μl). The vessel was attached to the tritiunn line, frozen in liquid nitrogen and evacuated. Tritium gas (342 mCi) was then added to the flask, which was stirred at room temperature for 2 hours. At the completion of the reaction, the excess tritium was removed and the reacted peptide solution was diluted with DMF (0.5 ml) and filtered to remove the catalyst. The collected DMF solution of the crude peptide was diluted with water and freeze dried to remove the labile tritium. The solid peptide was redissolved in water and the freeze drying process repeated. The tritiated peptide ([^HJhaTRAP) was dissolved in 0.5 ml of 0.1% aqueous TFA and purified by HPLC using the following conditions: column. Vydac C18, 25 cm x 9.4 mm I.D.; mobile phase, (A) 0.1% TFA in water, (B) 0.1% TFA in CH3CN; gradient, (A/B) from 100/0 to 40/60 over 30 min; flow rate, 5 ml /min; detection, UV at 215 nm. The radiochemical purity of [3H]haTRAP was 99% as analyzed by HPLC. A batch of 14.9 mCi at a specific activity of 18.4 Ci/mmol was obtained. Preparation of platelet membranes Platelet membranes were prepared using a modification of the method of Natarajan et al (Natarajan et at, Int. J. Peptide Protein Res. 45:145-151 (1995)) from . 20 units of platelet concentrates obtained from the North Jersey Blood Center (East Orange, NJ) within 48 hours of collection. All steps were carried out at 4° C under approved biohazard safety conditions. Platelets were centrifuged at 100 x g for 20 minutes at 4° C to remove red cells. The supernatants were decanted and centrifuged at 3000 X g for 15 minutes to pellet platelets. Platelets were resuspended in 10 mM Tris-HCI, pH 7.5,150 mM NaCI, 5 mM EDTA, to a total volume of 200 ml and centrifuged at 4400 x g for 10 minutes. This step was repeated two additional times. Platelets were resuspended in.5 mM Tris-HCI, pH 7.5, 5 mM EDTA to a final volume of approximately 30 ml and were homogenized with 20 strokes in a Dounce homogenizes Membranes were pelleted at 41,000 x g, resuspended in 40-50 ml 20 mM Tris-HCI, pH 7.5, 1 mM EDTA. 0.1 mM dithiothreltol, and 10 ml aliquots were frozen in liquid N2 and stored at -80° C. To complete membrane preparation, aliquots were thawed, pooled, and homogenized with 5 strokes of a Dounce homogenizer. Membranes were pelleted and washed 3 times in 10 mM triethanolamine-HCI, pH 7.4 5 mM EDTA, and resuspended in 20-25 ml 50 mM Tris-HCI, pH 7.5,10 mM MgCi2,1 mM EGTA. and 1% DMSO. Aliquots of membranes were frozen in liquid N2 and stored at -80° C. Membranes were stable for at least 3 months. 20 units of platelet concentrates typically yielded 250 mg of membrane protein. Protein concentration was determined by a Lowry assay (Lowry et al. J. Biol. Chem., 193:265-275 (1951)). High Throughput Thrombin Receptor Radioligand Binding Assay Thrombin receptor antagonists were screened using a modification of the thrombin receptor radioligand binding assay of Ahn et al, (Ahn et al, Mol. Pharmacol.. 51:350-356 (1997)). The assay was performed in 96 well Nunc plates (Cat. No. 269620) at a final assay volume of 200 pi. Platelet membranes and [^HjhaTRAP were diluted to 0.4 mg/ml and 22.2 nM, respectively, in binding buffer (50 mM Tris-HCI, pH 7.5. 10 mM MgCl2, 1 mM EGTA, 0.1% BSA). Stock solutions (10 mM in 100% DMSO) of test compounds were further diluted in 100% DMSO. Unless otherwise indicated, 10 pi of diluted compound solutions and 90 pi of radioligand (a final concentration of 10 nM in 5% DMSO) were added to each well, and the reaction was started by the addition of 100 pi of membranes (40 pg protein/well). The binding was not significantly inhibited by 5% DMSO. Compounds were tested at three concentrations (0.1,1 and 10 pM). The plates were covered and vortex-mixed gently on a Lab-Line Titer Plate Shaker for 1 hour at room temperature. Packard UniFilter GF/C filter plates were soaked for at least 1 hour in 0.1% polyethyleneimine. The incubated membranes were harvested using a Packard FilterMate Universal Harvester and were rapidly washed four times with 300 pi ice coW 50 mM Tris-HCI, pH 7.5. 10 mM MgCl2,1 mM EGTA. MicroScint 20 scintillation cocktail (25 pl) was added to each well, and the plates were counted in a Packard TopCount Microplate Scintillation Counter. The specific binding was defined as the total binding minus the nonspecific binding observed in the presence of excess (50 pM) unlabeled haTRAP. The % inhibition by a compound of [3H]haTRAP binding to thrombin receptors was. calculated from the following reiationsh'— % Inhibition = Total binding-Binding in the presence of a test compound x 100 Total binding-Nonspecific binding Materials A(pF-F)R(ChA)(hR)Y-NH2 and A(pF-F)R(ChA)(hR){l2-Y)-NH2, were custom synthesized by AnaSpec Inc. (San Jose, CA). The purity of these peptides was >95%. Tritium gas (97%) was purchased from EG&G Mound, Miamisburg Ohio. The gas was subsequently loaded and stored on an IN/US Systems Inc. Trisorber, MicroScint 20 scintillation cocktail was obtained from Packard Instrument Co. Protocol For Ex-Vivo Platelet Aggregation In Cynomolgus Whole Blood Drug administration and blood collection: Conscious chaired cynomolgus monkeys are allowed to equilibrate for 30 min, A needle catheter is inserted into a brachial vein for infusion of test drugs. Another needle catheter is inserted into the other brachial or saphenous vein and used for blood sampling. In those experiments where the compound is administered orally only one catheter is used. A baseline blood sample (1-2 ml) is collected in vacutainer tubes containing a thrombin inhibitor CVS 2139 (100 μg/0.1 ml saline) as an anticoaculant. The drug is then infused intravenously over a period of 30 min. Blood samples (1 ml) are collected at 5, 10, 20, 30 min during and 30, 60, 90 min after termination of the drug infusion. In PC experiments the animals are dosed with the drug using a gavage cannula. Blood samples are collected at 0, 30, 60, 90, 120,180, 240, 300, 360 min after dosing. 0.5 ml of the blood is used for whole blood aggregation and the other 0.5 ml is used for determining the plasma concentration.of the drug or its metabolites. Aggregation is performed immediately after collection of the blood sample as described below. Whole Blood Aggregation: A 0.5 ml blood sample is added to 0.5 ml of saline and warmed to 37°C in a Chronolog whole blood aggregometer. Simultaneously, the impedance electrode is warmed in saline to 37°C. The blood sample with a stir bar is place in the heating block well, the impedance electrode is placed in the blood sample and the collection software is started. The software is allowed to run until the baseline is stabilized and then a 20 Ω calibration check is performed. 20 Ω is equal to 4 blocks on the graphic produced by the computer software. The agonist (haTRAP) is added by an adjustable volume pipette (5-25 μl) and the aggregation curve is recorded for 10 minutes. Maximum aggregation in 6 minutes following agonist is the value recorded. In vitro Platelet Aggregation Procedure: Platelet aggregation studies were performed according to the method of Bednar et al. (Bednar, B., Condra, C, Gould, R.J., and Connolly, T.M., Throm. Res,, 77:453-463 (1995)). Blood was obtained from healthy human subjects who were aspirin free for at least 7 days by venipuncture using ACD as anticoagulant. Platelet rich plasma was prepared by centrifugation at 100Xg for 15 minutes at 15 deg C. Platelets were pelleted at 3000xg and washed twice in buffered saline containing 1 mM EGTA and 20 μg/ml apyrase to inhibit aggregation. Aggregation was performed at room temperature in buffered saline supplemented with 0.2 mg/ml human fibrinogen. Test compound and platelets were preincubated in 96-well flat-bottom plates for 60 minutes. Aggregation was initiated by adding 0.3 pM haTRAP or 0.1 U/ml thrombin and rapidly vortexing the mixture using a Lab Line Titer Plate Shaker (speed 7). Percent aggregation was monitored as increasing light transmittance at 405 nm in a Spectromax Plate Reader. In vivo Antitumor Procedure: Tests in the human breast carcinoma model in nude mouse are conducted according to the procedure reported in S. Even-Ram et al., Nature Medicine, 4, 8 (1988), p. 909-914. Using the test procedures described above, in the in vitro thrombin receptor antagonist assay, compounds of the invention were found to have IC50 values (i.e., the concentration at which a 50% inhibition of thrombin receptor was observed) in the range of about 1 to about 2000 nM, with preferred compounds fiaving IC50 values in the range of about 1 to about 100 nM. While the present invention has been described in conjunction with the specific embodiments set forth above, many alternatives, modifications and variations thereof will be apparent to those of ordinary skill in the art. All such altematives, modifications and variations are intended to fall within the spirit and scope of the present invention. 1. A compound represented by the structural formula R 21-aryl; aryl wherein adjacent carbons fomn a ring with a methylenedioxy group; and R21-heteroaryl; R and R are independently selected from the group consisting of H, C1-C6 7. A compound of claim 1 selected from the group consisting of compounds of the formula wherein W Is as defined in the following table: 8. A phamiaceutical composition comprising an effective amount of at least one compound of claim 1 and a pharmaceutically acceptable carrier. 9. A compound selected from the group consisting of compounds of the formula wherein W and Z are as defined in the following table: 10. A compound represented by the structural formula substantially as herein described and exemplified. Dated this 16 day of April 2004

Documents:

0793-chenp-2004-abstract.pdf

0793-chenp-2004-assignement.pdf

0793-chenp-2004-claims.pdf

0793-chenp-2004-correspondnece-others.pdf

0793-chenp-2004-correspondnece-po.pdf

0793-chenp-2004-description(complete).pdf

0793-chenp-2004-form 1.pdf

0793-chenp-2004-form 18.pdf

0793-chenp-2004-form 26.pdf

0793-chenp-2004-form 3.pdf

0793-chenp-2004-form 5.pdf

0793-chenp-2004-pct.pdf