IP Library Granted Patent US 10,941,162
Granted Patent B2
US 10,941,162 · App. 16/290,545 · Granted Mar 9, 2021

Heterocyclic compounds and uses thereof

Inventors: Alfredo C. Castro (Woburn, MA); Catherine A. Evans (Somerville, MA); Martin R. Tremblay (Melrose, MA)
Assignee: Infinity Pharmaceuticals, Inc.
C07D519/00C07D471/04C07D487/04C07D491/04C07D495/04C07D498/04C07D513/04
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Quick Facts
Patent No.
US 10,941,162
App. No.
16/290,545
Granted
Mar 9, 2021
Kind
B2
Abstract

Trisubstituted bicyclic heterocyclic compounds (e.g., pyridopyrimidinones) and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.

Claims (34)

1. A compound of Formula I′ or Formula II′:

or a pharmaceutically acceptable form thereof,

wherein

W d is a 3-14 membered heteroaryl; wherein the heteroaryl is optionally substituted with R 1f , R 2f , R 3f , R 4f , and R 5f ;

each instance of R 1a is independently selected from the group consisting of hydrogen, C 1 -C 8 alkyl, and 5-6 membered heteroaryl; wherein each of alkyl or heteroaryl is optionally substituted with one or more R 11 ;

each instance of R 11 is independently selected from the group consisting of hydrogen, C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, halo, OH, O(C 1 -C 8 alkyl), OCF 3 , OCF 2 H, OCFH 2 , NH 2 , NH(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl) 2 , haloalkyl, CN, NO 2 , CONH 2 , CONH(C 1 -C 8 alkyl), CON(C 1 -C 8 alkyl) 2 , COH, CO(C 1 -C 8 alkyl), COOH, COO(C 1 -C 8 alkyl), NHCO(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl)CO(C 1 -C 8 alkyl), (3-14 membered saturated, unsaturated, or aromatic carbocycle), and (3-14 membered saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of N, O, and S);

R 2a , R 3a , and R 4a each is hydrogen;

R 1b , R 2b , R 3b , R 4b , and R 5b each is hydrogen;

R 1c is selected from the group consisting of hydrogen, C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, halo, OH, O(C 1 -C 8 alkyl), OCF 3 , OCF 2 H, OCFH 2 , NH 2 , NH(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl) 2 , haloalkyl, CN, NO 2 , CONH 2 , CONH(C 1 -C 8 alkyl), CON(C 1 -C 8 alkyl) 2 , COH, CO(C 1 -C 8 alkyl), COOH, COO(C 1 -C 8 alkyl), NHCO(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl)CO(C 1 -C 8 alkyl), (3-14 membered saturated, unsaturated, or aromatic carbocycle), and (3-14 membered saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of N, O, and S);

R 2c is hydrogen or C 1 -C 8 alkyl;

R 1f is selected from the group consisting of NH 2 , NH(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl) 2 , hydrogen, C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, halo, OH, O(C 1 -C 8 alkyl), OCF 3 , OCF 2 H, OCFH 2 , haloalkyl, CN, NO 2 , CONH 2 , CONH(C 1 -C 8 alkyl), CON(C 1 -C 8 alkyl) 2 , COH, CO(C 1 -C 8 alkyl), COOH, COO(C 1 -C 8 alkyl), NHCO(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl)CO(C 1 -C 8 alkyl), (3-14 membered saturated, unsaturated, or aromatic carbocycle), and (3-14 membered saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of N, O, and S); and

R 2f , R 3f , R 4f , and R 5f each is independently selected from the group consisting of hydrogen, C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, halo, OH, O(C 1 -C 8 alkyl), OCF 3 , OCF 2 H, OCFH 2 , NH 2 , NH(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl) 2 , haloalkyl, CN, NO 2 , CONH 2 , CONH(C 1 -C 8 alkyl), CON(C 1 -C 8 alkyl) 2 , COH, CO(C 1 -C 8 alkyl), COOH, COO(C 1 -C 8 alkyl), NHCO(C 1 -C 8 alkyl), N(C 1 -C 8 alkyl)CO(C 1 -C 8 alkyl), (3-14 membered saturated, unsaturated, or aromatic carbocycle), and (3-14 membered saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of N, O, and S).

2. The compound of claim 1 , which is a compound of Formula I′:

or a pharmaceutically acceptable form thereof.

3. The compound of claim 1 , which is a compound of Formula II′:

or a pharmaceutically acceptable form thereof.

4. The compound of claim 2 , wherein the compound of Formula I′ is a compound of formula I:

or a pharmaceutically acceptable form thereof.

5. The compound of claim 3 , wherein the compound of Formula II′ is a compound of formula II:

or a pharmaceutically acceptable form thereof.

6. The compound of claim 2 , wherein the compound of Formula I′ is a compound of the formula:

or a pharmaceutically acceptable form thereof.

7. The compound of claim 2 , wherein the compound of Formula I′ is a compound of the formula:

or a pharmaceutically acceptable form thereof.

8. The compound of claim 1 , which is

or a pharmaceutically acceptable salt thereof.

9. The compound of claim 4 , wherein R 1f is NH 2 , NH(C 1 -C 8 alkyl), or N(C 1 -C 8 alkyl) 2 .

10. The compound of claim 9 , wherein R 1f is NH 2 .

11. The compound of claim 4 , wherein R 2f , R 3f , and R 4f each is independently hydrogen, C 1 -C 8 alkyl, C 2 -C 8 alkenyl, or C 2 -C 8 alkynyl.

12. The compound of claim 11 , wherein R 2f , R 3f , and R 4f are hydrogen.

13. The compound of claim 1 , which is

or a pharmaceutically acceptable salt thereof.

14. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable expedient.

15. The pharmaceutical composition of claim 14 , further comprising one or more therapeutic agents.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2024
From: INFINITY PHARMACEUTICALS, INC.
To: TWELVE THERAPEUTICS, INC.
Reel/Frame 069193/0925 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2019
From: CASTRO, ALFREDO C.; EVANS, CATHERINE A.; TREMBLAY, MARTIN R.
To: INFINITY PHARMACEUTICALS, INC.
Reel/Frame 049804/0420 →
Continuity (5)
Division 15621815 · Jun 13, 2017
Continuation 14874328 · Oct 2, 2015
Provisional Application 62216261 · Sep 9, 2015
Provisional Application 62059426 · Oct 3, 2014
Related Publication 20190330240A1 · Oct 31, 2019