SUBSTITUTED (1,2,3,4-TETRAHYDROCYCLOPENTA[b]INDOL-3-YL)ACETIC ACID DERIVATIVES USEFUL IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISORDERS

Abstract

Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of S1P1 receptor-associated disorders, for example, psoriasis, rheumatoid arthritis, Crohn's disease, transplant rejection, multiple sclerosis, systemic lupus erythematosus, ulcerative colitis, type I diabetes, acne, microbial infections or diseases and viral infections or diseases.

1 - 58 . (canceled) 
     
     
         59 . A composition comprising a compound selected from compounds of Formula (Ik) and pharmaceutically acceptable salts, solvates and hydrates thereof: 
       
         
           
           
               
               
           
         
         and a pharmaceutically acceptable carrier; 
         wherein: 
         Y is N or CR 1 ; 
         Z is N or CR 4 ; 
         R 1  is H or C 1 -C 6  haloalkyl; 
         R 2  is selected from the group consisting of H, cyano, C 1 -C 6  haloalkoxy and C 1 -C 6  haloalkyl; 
         R 3  is selected from the group consisting of H, C 1 -C 6  alkoxy, C 1 -C 6  alkyl, C 3 -C 7  cycloalkyl, C 1 -C 6  haloalkoxy, C 1 -C 6  haloalkyl, halogen and heterocyclyl; and 
         R 4  is selected from the group consisting of H, cyano and C 1 -C 6  haloalkyl. 
       
     
     
         60 . The composition according to  claim 59 , wherein Y is CR 1 . 
     
     
         61 . The composition according to  claim 59 , wherein R 1  is H or trifluoromethyl. 
     
     
         62 . The composition according to  claim 59 , wherein R 2  is selected from the group consisting of H, cyano, C 1 -C 6  haloalkoxy and C 1 -C 6  haloalkyl. 
     
     
         63 . The composition according to  claim 59 , wherein R 2  is selected from the group consisting of H, cyano, trifluoromethoxy and trifluoromethyl. 
     
     
         64 . The composition according to  claim 59 , wherein;
 R 3  is selected from the group consisting of H, carboxamide, chloro, cyano, cyclobutyl, cyclohexyl, cyclopentyl, cyclopentyloxy, cyclopropyl, cyclopropylmethoxy, cyclohexylmethyl, 3,3-difluoropyrrolidin-1-yl, ethylamino, isobutyl, isopropoxy, methylsulfonyl, neopentyl, propyl, pyrrolidin-1-yl, 1,2,3-thiadiazol-4-yl, trifluoromethoxy and trifluoromethyl.   
     
     
         65 . The composition according to  claim 59 , wherein
 R 4  is selected from the group consisting of H, cyano, trifluoromethoxy, and trifluoromethyl.   
     
     
         66 . The composition according to  claim 59 , wherein the compound is selected from the following compounds and pharmaceutically acceptable salts, solvates and hydrates thereof:
 2-(7-(3-cyano-5-(trifluoromethoxy)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid;   2-(7-(3-cyano-4-isopropoxybenzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid;   2-(7-(3-cyano-4-(trifluoromethoxy)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid;   2-(7-(2,4-bis(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid; and   2-(7-(3,5-bis(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid.   
     
     
         67 . The composition according to  claim 59 , wherein (New) The composition is suitable for oral administration. 
     
     
         68 . The composition according to  claim 59 , wherein the pharmaceutically acceptable carrier comprises a diluent. 
     
     
         69 . A method for treating a disorder associated with the S1P1 receptor in an individual comprising administering to said individual in need thereof a therapeutically effective amount of
 a compound selected from compounds of Formula (Ik) and pharmaceutically acceptable salts, solvates and hydrates thereof:   
       
         
           
           
               
               
           
         
         and a pharmaceutically acceptable carrier; 
         wherein: 
         Y is N or CR 1 ; 
         Z is N or CR 4 ; 
         R 1  is H or C 1 -C 6  haloalkyl; 
         R 2  is selected from the group consisting of H, cyano, C 1 -C 6  haloalkoxy and C 1 -C 6  haloalkyl; 
         R 3  is selected from the group consisting of H, C 1 -C 6  alkoxy, C 1 -C 6  alkyl, C 3 -C 7  cycloalkyl, C 1 -C 6  haloalkoxy, C 1 -C 6  haloalkyl, halogen and heterocyclyl; and 
         R 4  is selected from the group consisting of H, cyano and C 1 -C 6  haloalkyl; 
         wherein said disorder associated with the S1P1 receptor is selected from the group consisting of: psoriasis, rheumatoid arthritis, acne, psoriatic arthritis, inflammatory bowel disease, Crohn's disease, transplant rejection, multiple sclerosis, biliary cirrhosis, systemic lupus erythematosus, ulcerative colitis, and type I diabetes. 
       
     
     
         70 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is multiple sclerosis. 
     
     
         71 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is psoriasis. 
     
     
         72 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is rheumatoid arthritis. 
     
     
         73 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is Crohn's disease. 
     
     
         74 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is psoriatic arthritis transplant rejection. 
     
     
         75 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is systemic lupus erythematosus. 
     
     
         76 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is ulcerative colitis. 
     
     
         77 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is inflammatory bowel disease type I diabetes. 
     
     
         78 . The method according to  claim 69 , wherein said disorder associated with the S1P1 receptor is biliary cirrhosis.