US2020206221A1PendingUtilityA1

Beta-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes

Assignee: MERCK SHARP & DOHMEPriority: Jul 6, 2001Filed: Mar 6, 2020Published: Jul 2, 2020
Est. expiryJul 6, 2021(expired)· nominal 20-yr term from priority
C07D 487/04A61P 37/02A61P 9/10A61P 15/16A61P 5/50A61K 45/06A61P 3/04A61P 13/08A61K 31/4985A61K 31/498A61P 1/04A61P 43/00A61P 25/28A61P 13/12A61P 25/00A61P 31/18A61P 35/04A61P 3/00A61P 5/06A61P 9/08A61P 5/28A61P 1/02A61P 31/10A61K 38/28A61P 3/06A61P 7/00A61P 3/10A61P 27/02A61P 9/12A61P 19/10Y10S514/866
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Claims

Abstract

The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.

Claims

exact text as granted — not AI-modified
1 - 40 . (canceled) 
     
     
         41 . A pharmaceutical composition comprising
 (1) a first compound of the formula:   
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof; 
         (2) an α-glucosidase inhibitor; and 
         (3) a pharmaceutically acceptable carrier. 
       
     
     
         42 . The pharmaceutical composition of  claim 41  wherein the α-glucosidase inhibitor is acarbose. 
     
     
         43 . A method of treating Type 2 diabetes comprising administering to a mammalian patient in need of such treatment a therapeutically effective amount of a first compound of the formula: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof; and an α-glucosidase inhibitor. 
       
     
     
         44 . The method of  claim 43  wherein the α-glucosidase inhibitor is acarbose.

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