Tricyclic heterocyclic compounds as phosphoinositide 3-kinase inhibitors

Abstract

or a pharmaceutically acceptable salt thereof, wherein: W is O, N—H, N—(C1-C10 alkyl) or S; each X is independently CH or N; R1 is a 5 to 7-membered saturated or unsaturated, optionally substituted heterocycle containing at least 1 heteroatom selected from N or O; R2 is LY; each L is a direct bond, C1-C10 alkylene, C2-C10 alkenylene or C2-C10 alkynylene; Y is an optionally substituted fused, bridged or spirocyclic non-aromatic 5-12 membered heterocycle containing up to 4 heteroatoms selected from N or O; and each R3 is independently H, C1-C10 alkyl, halogen, fluoro C1-C10 alkyl, O—C1-C10 alkyl, NH—C1-C10 alkyl, S—C1-C10 alkyl, O-fluoro C1-C10 alkyl, NH-acyl, NH—C(O)—NH—C1-C10 alkyl, C(O)—NH—C1-C10 alkyl, aryl or heteroaryl, are useful as inhibitors of the class IA phosphoinositide 3-kinase enzyme, PI3K-p110δ, and therefore have potential utility in the therapy of cancer, immune and inflammatory diseases.

1 - 21 . (canceled) 
     
     
         22 . A method of treating a cancer in a patient in need thereof, wherein the cancer is selected from the group consisting of a leukaemia, lymphoma, solid tumour, and PTEN-negative tumour, the method comprising administering to the patient a therapeutically effective amount of a compound represented by: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof, wherein:
 R 33  is independently selected for each occurrence from the group consisting of H, halogen, NH—C 1-3 alkyl, NH 2 , C 1-6 alkyl and —O—C 1-6 alkyl, wherein C 1-6 alkyl for each occurrence is optionally substituted by one, two or three substituents selected from halogen or hydroxyl; 
 R 34  is selected from H or C 1-3 alkyl; and 
 R 44  and R 45 , when taken together with the nitrogen to which they are attached form a 7-10 membered bicyclic spirocycle or bridged heterocycle each having an additional heteroatom selected from the group consisting of O, S, and NR 55 , wherein R 55  is H or C 1-3 alkyl. 
 
       
     
     
         23 . The method of  claim 22 , wherein R 44  and R 45 , when taken together with the nitrogen to which they are attached form a 7-8 membered bicyclic bridged heterocycle represented by: 
       
         
           
           
               
               
           
         
       
       wherein:
 D is selected from the group consisting of O, S and NR 55 ; 
 E is (CH 2 ) r , wherein r is 1 or 2, 
 V is O or NR 5 , and 
 R 55  is H or C 1-3 alkyl. 
 
     
     
         24 . The method of  claim 22 , wherein R 44  and R 45 , when taken together with the nitrogen to which they are attached form a 7-10 membered spirocycle having one additional heteroatom selected from O or NR 5 , wherein R 55  is H or C 1-3 alkyl 
     
     
         25 . The method of  claim 22 , wherein the PTEN-negative tumor is selected from the group consisting of PTEN-negative haematological, breast, lung, endometrial, skin, brain and prostate cancers. 
     
     
         26 . The method of  claim 22 , wherein the cancer is leukaemia or lymphoma. 
     
     
         27 . A method of treating a cancer in a patient in need thereof, wherein the cancer is selected from the group consisting of a leukaemia, lymphoma, solid tumour, and PTEN-negative tumour, the method comprising administering to the patient a therapeutically effective amount of a compound represented by: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof. 
       
     
     
         28 . The method of  claim 27 , wherein the PTEN-negative tumor is selected from the group consisting of PTEN-negative haematological, breast, lung, endometrial, skin, brain and prostate cancers. 
     
     
         29 . The method of  claim 27  wherein the cancer is leukaemia or lymphoma. 
     
     
         30 . A compound represented by: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof.