US2017050942A1PendingUtilityA1

3-cycloalkylaminopyrrolidine derivatives as modulators of chemokine receptors

Assignee: INCYTE CORPPriority: Dec 18, 2003Filed: Nov 4, 2016Published: Feb 23, 2017
Est. expiryDec 18, 2023(expired)· nominal 20-yr term from priority
A61P 3/10A61P 37/02A61P 43/00A61P 9/08A61P 37/00A61P 37/06A61P 9/10A61P 31/12A61P 25/04A61P 35/00A61P 3/04A61P 31/18A61P 29/00A61P 25/00C07D 401/14C07D 277/24C07D 413/14A61P 19/02C07D 207/14A61P 19/00C07D 401/12A61K 31/501C07D 417/12A61K 31/4439C07D 413/12C07D 403/12A61K 31/427A61K 31/497A61P 17/00A61K 31/4025C07D 417/14C07D 417/04A61K 31/454A61K 31/506A61K 31/40A61K 31/5377A61P 15/00
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Claims

Abstract

The present invention relates to 3-cycloalkylaminopyrrolidine derivatives of the formula I: (wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , X, Y and Z are as defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of chemokine receptors and more specifically as modulators of the CCR2 and/or CCR5 receptor. The compounds and compositions of the invention may bind to chemokine receptors, e.g., the CCR2 and/or CCR5 chemokine receptors, and are useful for treating diseases associated with chemokine, e.g., CCR2 and/or CCR5, activity, such as atherosclerosis, restenosis, lupus, organ transplant rejection and rheumatoid arthritis.

Claims

exact text as granted — not AI-modified
1 - 57 . (canceled) 
     
     
         58 . A method of preparing a compound of formula 7-7, 
       
         
           
           
               
               
           
         
       
       comprising the steps of
 (1) reacting a compound of 
 
       
         
           
           
               
               
           
         
       
       with a compound of 
       
         
           
           
               
               
           
         
       
       under a first suitable condition, to obtain a compound of 
       
         
           
           
               
               
           
         
         (2) converting the compound of 
       
       
         
           
           
               
               
           
         
       
       under a second suitable condition to obtain a compound of 
       
         
           
           
               
               
           
         
       
       and
 (3) treating the compound of 
 
       
         
           
           
               
               
           
         
       
       under an acidic condition to obtain the compound of formula 7-7.

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