US2014005400A1PendingUtilityA1

New azacyclic compounds

Assignee: HOFFMANN LA ROCHEPriority: Aug 13, 2010Filed: Aug 29, 2013Published: Jan 2, 2014
Est. expiryAug 13, 2030(~4 yrs left)· nominal 20-yr term from priority
A61P 9/00A61P 3/06A61P 3/10A61P 9/10A61P 43/00A61K 31/437C07D 471/10A61P 3/04A61P 3/00A61K 31/438
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Claims

Abstract

The invention provides novel compounds having the general formula (I) wherein R 1 , R 2 and n are as described herein, compositions including the compounds and methods of using the compounds. The compounds are useful as inhibitors of hormone sensitive lipase (HSL) for the treatment of diabetes, metabolic syndrome and obesity.

Claims

exact text as granted — not AI-modified
1 - 12 . (canceled) 
     
     
         13 . A compound according to formula (I) 
       
         
           
           
               
               
           
         
         wherein: 
         R 1  is selected from the group consisting of: imidazolyl, pyrazolyl, triazolyl, phenyl, pyridinyl, pyrazinyl, pyrimidyl, pyridazinyl and 2-oxo-1,2-dihydro-pyridinyl, 
         and is optionally substituted with one to three substituents independently selected from the group consisting of alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkoxyalkyl, cycloalkoxy, cycloalkoxyalkyl, alkylcycloalkylalkyl, halocycloalkyl, halocycloalkylalkyl, halogen, haloalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, haloalkoxy, hydroxyalkoxy, alkoxyalkoxy, alkoxyalkoxyalkyl and hydroxyhaloalkyl; 
         R 2  is pyridinyl or 2-oxo-1,2-dihydro-pyridinyl, 
         and is optionally substituted with one to three substituents independently selected from alkyl and hydroxy; and 
         n is zero; 
         or a pharmaceutically acceptable salt thereof.

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