US2006069148A1PendingUtilityA1

Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment

57
Assignee: BERTHELETTE CARLPriority: Jan 24, 2002Filed: Nov 4, 2005Published: Mar 30, 2006
Est. expiryJan 24, 2022(expired)· nominal 20-yr term from priority
A61P 9/04A61P 35/04A61P 37/06A61P 37/02A61P 7/02A61P 43/00A61P 9/08A61P 9/10A61P 37/08A61P 29/00A61P 25/06A61P 27/02A61P 29/02A61P 3/10A61P 27/16A61P 27/06A61P 25/04A61P 25/20A61P 35/00A61P 19/10A61P 11/00A61P 11/02A61P 11/06A61P 19/00A61P 19/02A61P 19/08A61P 15/06A61P 15/00A61P 13/08C07D 209/88C07D 209/80A61K 31/404
57
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Claims

Abstract

Fluoro substituted cycloalkanoindole derivatives are antagonists of prostaglandins, and as such are useful for the treatment of prostaglandin mediated diseases.

Claims

exact text as granted — not AI-modified
1 . A compound of formula I:  
       
         
           
           
               
               
           
         
         and pharmaceutically acceptable salts thereof, wherein  
         n is 0 or 1; m is 1, 2 or 3; R 1  is H, C 1 -C 3  alkyl, halogenated C 1 -C 3  alkyl or cyclopropyl; R 2  is 4-chlorophenyl or 2,4,6-trichlorophenyl.  
       
     
     
         2 . The compound of  claim 1  wherein n is 0.  
     
     
         3 . The compound of  claim 1  wherein n is 1.  
     
     
         4 . The compound of  claim 1  wherein m is 1.  
     
     
         5 . (canceled)  
     
     
         6 . The compound of  claim 1  wherein R 1  is H.  
     
     
         7 . The compound of  claim 1  wherein R 1  is CH 3 .  
     
     
         8 . The compound of  claim 1  wherein R 2  is 4-chlorophenyl.  
     
     
         9 . (canceled)  
     
     
         10 . The compound of  claim 1  having the stereoconfiguration shown below:  
       
         
           
           
               
               
           
         
       
     
     
         11 . The compound of  claim 10  wherein n is 0.  
     
     
         12 . The compound of  claim 10  wherein n is 1.  
     
     
         13 . The compound of  claim 10  wherein m is 1.  
     
     
         14 . (canceled)  
     
     
         15 . The compound of  claim 10  wherein R 1  is H.  
     
     
         16 . The compound of  claim 10  wherein R 1  is CH 3 .  
     
     
         17 . The compound of  claim 10  wherein R 2  is 4-chlorophenyl.  
     
     
         18 . (canceled)  
     
     
         19 . A compound selected from 
 [4-(4-chlorobenzyl)-7-fluoro-5-(methanesulfonyl)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl]acetic acid,    {4-[1-(4-chlorophenyl)ethyl]-7-fluoro-5-methanesulfonyl-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl}acetic acid,    [9-(4-chlorobenzyl)-6-fluoro-8-methanesulfonyl-2,3,4,9-tetrahydro-1H-carbazol-1-yl]acetic acid, and    [4-(4-chlorobenzyl)-7-fluoro-5-methanesulfonyl-1-oxo-1,2,3,4-tetrahydro-cyclopenta[b]indol-3-yl]acetic acid, or    a pharmaceutically acceptable salt thereof.    
     
     
         20 . The compound (3R)-[4-(4-chlorobenzyl)-7-fluoro-5-(methanesulfonyl)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl]acetic acid and pharmaceutically acceptable salts thereof.  
     
     
         21 - 23 . (canceled)  
     
     
         24 . A pharmaceutical composition comprising a compound of  claim 1  and a pharmaceutically acceptable carrier.  
     
     
         25 . The composition of  claim 24  further comprising a second active ingredient selected from an antihistamine, a leukotriene antagonist and a leukotriene biosynthesis inhibitor.  
     
     
         26 - 29 . (canceled)  
     
     
         30 . The composition of  claim 24  further comprising nicotinic acid.

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