Pyrazolo[3,4-d]pyrimidine and pyrazolo[2,3-d]pyrimidine compounds as kinase inhibitors
View Patent ↗Disclosed herein are compounds such as those of Formula (I) that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. Methods for the preparation of the compounds are disclosed. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the Btk inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
1. A compound having the structure of Formula (I):
wherein:
A is —CH—;
R 20 is halogen, —CN, —NO 2 , —OH, —N(R 21 )C(═O)R 23 , —C(═O)N(R 21 )(R 22 ), —OR 27 , —CO 2 H, —O— alkylene-CO 2 H, —O-alkylene-C(═O)N(R 21 )(R 22 ), —N(R 21 )C(═O)N(R 21 )(R 22 ), C 1 -C 2 alkyl optionally substituted with at least one R 28 , C 2 -C 6 alkenyl optionally substituted with at least one R 28 , or C 2 -C 6 alkynyl optionally substituted with at least one R 31 ;
each R 21 is independently H, substituted or unsubstituted C 1 -C 6 alkyl, or substituted or unsubstituted C 3 -C 8 cycloalkyl;
each R 22 is independently H, substituted or unsubstituted C 1 -C 6 alkyl, or substituted or unsubstituted C 3 -C 8 cycloalkyl;
each R 23 is independently substituted or unsubstituted C 1 -C 6 alkyl, or substituted or unsubstituted C 3 -C 8 cycloalkyl;
R 27 is substituted or unsubstituted C 3 -C 8 cycloalkyl or C 1 -C 6 alkyl substituted with alkoxy;
each R 24 is independently halogen, —CN, —NO 2 , —OH, —OCF 3 , —OCH 2 F, —OCF 2 H, —CF 3 , —SCH 3 , —N(R 21 )S(═O) 2 R 23 , —S(═O) 2 N(R 21 )(R 22 ), —S(═O)R 23 , —S(═O) 2 R 23 , —C(═O)R 23 , —OC(═O)R 23 , —CO 2 R 21 , —N(R 29 )(R 30 ), —C(═O)N(R 21 )(R 22 ), —N(R 21 )C(═O)R 23 , —N(R 21 )C(═O)OR 22 , —N(R 21 )C(═O)N(R 21 )(R 22 ), unsubstituted alkoxy, unsubstituted heteroalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted cycloalkyl, or C 1 -C 2 alkyl optionally substituted with at least one R 27 ;
R 28 is halogen, —CN, —NO 2 , —OH, or substituted or unsubstituted C 3 -C 6 cycloalkyl;
R 29 is H, CH 3 , substituted or unsubstituted cycloalkyl;
R 30 is H, CH 3 , or substituted or unsubstituted cycloalkyl;
R 31 is independently halogen, —CN, —NO 2 , —OH, —OCF 3 , —OCH 2 F, —OCF 2 H, —CF 3 , —SR 21 , —N(R 21 )S(═O) 2 R 23 , —S(═O) 2 N(R 21 )(R 22 ), —S(═O)R 23 , —S(═O) 2 R 23 , —C(═O)R 23 , —OC(═O)R 23 , —CO 2 R 21 , —N(R 29 )(R 30 ), —C(═O)N(R 21 )(R 22 ), —N(R 21 )C(═O)R 23 , —N(R 21 )C(═O)OR 22 , —N(R 21 )C(═O)N(R 21 )(R 22 ), substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted alkoxy, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heterocycloalkyl, or substituted or unsubstituted cycloalkyl;
n is 0-4; or
when n is 1-4, R 20 and R 24 together with the carbon atoms to which they are attached form a ring;
Y is an optionally substituted group selected from among alkylene, heteroalkylene, arylene, heteroarylene, alkylenearylene, alkyleneheteroarylene, alkylenecycloalkylene, alkyleneheterocycloalkylene, cycloalkylene, and heterocycloalkylene;
Z is —C(═O), —N(R a )C(═O), —N(R a )S(═O) x , where x is 1 or 2, and R a is H, substituted or unsubstituted alkyl, or substituted or unsubstituted cycloalkyl; and
R 6 is H or L-J-W;
R 7 and R 8 are independently H or L-J-W; or R 7 and R 8 taken together form a bond;
L and J are each independently a bond, substituted or unsubstituted C 1 -C 6 alkylene, substituted or unsubstituted C 3 -C 6 cycloalkylene, substituted or unsubstituted C 1 -C 6 heteroalkylene, substituted or unsubstituted C 2 -C 7 heterocycloalkylene, substituted or unsubstituted C 6 -C 12 arylene, substituted or unsubstituted C 3 -C 12 heteroarylene, —CO—, —O—, or —S—;
W is H, or NR 25 R 26 ;
R 25 and R 26 are each independently H, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 3 -C 6 cycloalkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 2 -C 7 heterocycloalkyl, substituted or unsubstituted C 6 -C 12 aryl, or substituted or unsubstituted C 3 -C 12 heteroaryl; or
a pharmaceutically acceptable salt thereof.
2. The compound of claim 1 , wherein R 20 is halogen and n is 0.
3. The compound of claim 1 , wherein Y is heterocycloalkylene.
4. The compound of claim 3 , wherein Z is —C(═O).
5. The compound of claim 1 , wherein R 6 , R 7 , and R 8 are each H.
6. Any one of compounds selected from
or
a pharmaceutically acceptable salt thereof.
7. A pharmaceutical composition comprising a pharmaceutically acceptable excipient and a compound of claim 1 or a pharmaceutically acceptable salt thereof.