US2018325911A1PendingUtilityA1

Novel compounds

Assignee: GLAXO GROUP LTDPriority: Apr 30, 2009Filed: May 16, 2018Published: Nov 15, 2018
Est. expiryApr 30, 2029(~2.8 yrs left)· nominal 20-yr term from priority
A61P 9/10A61P 7/00A61P 37/06A61P 37/08A61P 7/02A61P 43/00A61P 3/10A61P 37/00A61P 9/00A61P 25/04A61P 25/28A61P 31/10A61P 25/00A61P 35/00A61P 33/02A61P 31/04A61P 35/02A61P 29/02A61P 31/12A61P 29/00A61P 31/00A61P 15/08A61P 19/02A61P 11/00A61P 13/12A61P 1/18A61P 11/06A61P 1/16A61P 17/00A61P 1/00A61P 11/02C07D 413/14A61K 31/5377A61K 45/06A61K 31/535C07B 2200/13A61K 31/496A61K 31/5375A61K 31/497Y02A50/409Y02A50/30
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Claims

Abstract

and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular PI3-kinase activity.

Claims

exact text as granted — not AI-modified
1 - 12 . (canceled) 
     
     
         13 . A compound of formula (I): 
       
         
           
           
               
               
           
         
         wherein 
         R 1  is 9- or 10-membered bicyclic heteroaryl wherein the 9- or 10-membered bicyclic heteroaryl contains from one to three heteroatoms independently selected from oxygen and nitrogen and is optionally substituted by C 1-6 alkyl, C 3-6 cycloalkyl, halo, —CN or —NHSO 2 R 5 , or 
         pyridinyl optionally substituted by one or two substituents independently selected from C 1-6 alkyl, —OR 6 , halo and —NHSO 2 R 7 ; 
         R 2  and R 3 , together with the nitrogen atom to which they are attached, are linked to form a 6- or 7-membered heterocyclyl wherein the 6- or 7-membered heterocyclyl optionally contains an oxygen atom or a further nitrogen atom; 
         R 4  is hydrogen or methyl; 
         R 6  is hydrogen or C 1-4 alkyl; and 
         R 5  and R 7  are each independently C 1-6 alkyl, or phenyl optionally substituted by one or two substituents independently selected from halo; 
         or a salt thereof. 
       
     
     
         14 . The compound according to  claim 13 , wherein R 1  is
 9-membered bicyclic heteroaryl wherein the 9-membered bicyclic heteroaryl contains one or two nitrogen atoms, or pyridinyl optionally substituted by one or two substituents independently selected from —OR 6  and —NHSO 2 R 7 .   
     
     
         15 . A compound according to  claim 13 , wherein R 1  is indolyl. 
     
     
         16 . A compound according to  claim 13 , wherein R 1  is pyridinyl optionally substituted by one or two substituents independently selected from —OR 6  and —NHSO 2 R 7 . 
     
     
         17 . A compound according to  claim 13 , wherein R 2  and R 3 ,
 together with the nitrogen atom to which they are attached, are linked to form a 6-membered heterocyclyl wherein the 6-membered heterocyclyl optionally contains an oxygen atom or a further nitrogen atom.   
     
     
         18 . A compound according to  claim 13 , wherein R 2  and R 3 , together with the nitrogen atom to which they are attached, are linked to form a 6-membered heterocyclyl wherein the 6-membered heterocyclyl contains an oxygen atom. 
     
     
         19 . A compound according to  claim 13 , wherein R 2  and R 3 , together with the nitrogen atom to which they are attached, are linked to form a 6-membered heterocyclyl wherein the 6-membered heterocyclyl contains a further nitrogen atom. 
     
     
         20 . A compound according to  claim 13 , wherein R 4  is hydrogen. 
     
     
         21 . A compound according to  claim 13  wherein the compound of formula (I) is in the form of a pharmaceutically acceptable salt thereof.

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