IP Library Granted Patent US 11,401,256
Granted Patent B2
US 11,401,256 · App. 16/809,345 · Granted Aug 2, 2022

Dihydroquinolinones for medical treatment

Inventors: Roger Norcross (Basel, CH); Adrian Britschgi (Basel, CH); Fabian Dey (Basel, CH); Annick Goergler (Basal, CH); Eric Andre Kusznir (Basel, CH); Moreno Attilio Wichert (Basel, CH)
Assignee: C4 Therapeutics, Inc.
C07D401/04C07D401/14C07D413/14C07D471/04C07D519/00
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Quick Facts
Patent No.
US 11,401,256
App. No.
16/809,345
Granted
Aug 2, 2022
Kind
B2
Abstract

The present invention provides dihydroquinolinone compounds which bind to the ubiquitously expressed E3 ligase protein cereblon (CRBN) and alter the substrate specificity of the CRBN E3 ubiquitin ligase complex, resulting in breakdown of intrinsic downstream proteins. The disclosed compounds are useful for the treatment of cancer.

Claims (58)

1. A compound of the formula:

or a pharmaceutically acceptable salt thereof

wherein

X 1 is N or CH;

X 3 is N or CH;

and if one of X 1 or X 3 is nitrogen, the other one is CH;

R 3 is selected from: —(CH 2 ) 0-1 -aryl substituted by 1-2 substituents selected from R 4 , —(CH 2 ) 0-2 —N(R 3c )C(═O)—C 3-7 cycloalkyl, amino-C 1-6 alkyl, —C(═O)N(R 3a ,R 3b ) C(═O)O—C 1-6 alkyl, C 1-6 alkyl, and —C 3-7 cycloalkyl;

wherein one of the R 3 substituents is selected from —C(═O)N(R 3a ,R 3b ) and C(═O)O—C 1-6 alkyl;

R 3a is selected from hydrogen and C 1-6 alkyl;

R 3b is selected hydrogen and C 1-6 alkyl;

or R 3a and R 3b form together with the nitrogen to which they are attached form a heterocycloalkyl;

R 3c is hydrogen; and

R 4 is selected from amino, —C(═O)N(R 3a ,R 3b ), C 1-6 alkoxy, C 1-6 alkyl, halo-C 1-6 alkyl, and hydroxy-C 1-6 alkyl.

2. The compound of claim 1 , wherein X 1 is N.

3. The compound of claim 1 , wherein X 3 is N.

4. The compound of claim 1 , wherein R 3 is aryl substituted by 1-2 substituents selected from R 4 , wherein R 4 is selected from —C(═O)N(R 3a ,R 3b ), C 1-6 alkyl, and C 1-6 alkoxy.

5. The compound of claim 1 , wherein R 3 is aryl substituted by 1-2 substituents selected from R 4 , wherein R 4 is selected from C 1-6 alkoxy, C 1-6 alkyl, halo-C 1-6 alkyl, and hydroxy-C 1-6 alkyl.

6. The compound of claim 1 , wherein R 3 is —C(═O)N(R 3a ,R 3b ).

7. The compound of claim 6 , wherein R 3a is hydrogen and R 3b is C 1-6 alkyl.

8. The compound of claim 7 , wherein R 3b is methyl.

9. The compound of claim 1 of the formula:

or a pharmaceutically acceptable salt thereof.

10. The compound of claim 1 of the formula:

or a pharmaceutically acceptable salt thereof.

11. The compound of claim 1 of the formula:

or a pharmaceutically acceptable salt thereof.

12. The compound of claim 1 of the formula:

or a pharmaceutically acceptable salt thereof.

13. A compound of the formula:

or a pharmaceutically acceptable salt thereof

wherein

X 1 is N or CH;

X 3 is N or CH;

and if one of X 1 or X 3 is nitrogen, the other one is CH;

R 3 is selected from: —C(═O)N(R 3a ,R 3b ), C(═O)O—C 1-6 alkyl, unsubstituted heteroaryl, and heteroaryl substituted by 1-2 substituents selected from R 4 ;

wherein one of the R 3 substituents is selected from —C(═O)N(R 3a ,R 3b ) and C(═O)O—C 1-6 alkyl;

R 3a is selected from hydrogen and C 1-6 alkyl;

R 3b is selected hydrogen and C 1-6 alkyl;

R 3c is hydrogen;

R 4 is selected from amino, —(CH 2 ) 0-2 —N(R 3c )C(═O)—C 1-6 alkyl, —C(═O)—C 1-6 alkyl, —C(═O)N(R 3a ,R 3b ), C 1-6 alkoxy, C 1-6 alkyl, halo-C 1-6 alkyl, heteroaryl substituted by 1-2 substituents selected from R 5 , and hydroxy-C 1-6 alkyl; and

R 5 is C 1-6 alkyl.

14. The compound of claim 13 , wherein X 1 is N.

15. The compound of claim 13 , wherein X 3 is N.

16. The compound of claim 13 , wherein R 3 is heteroaryl substituted by 1 or 2 substituents selected from R 4 wherein R 4 is selected from —C(═O)N(R 3a ,R 3b ), C 1-6 alkyl, and C 1-6 alkoxy.

17. The compound of claim 13 , wherein R 3 is unsubstituted heteroaryl.

18. The compound of claim 13 , wherein R 3 is —C(═O)N(R 3a ,R 3b ).

19. The compound of claim 18 , wherein R 3a is hydrogen and R 3b is C 1-6 alkyl.

20. The compound of claim 19 , wherein R 3b is methyl.

21. The compound of claim 13 of the formula:

or a pharmaceutically acceptable salt thereof.

22. The compound of claim 13 of the formula:

or a pharmaceutically acceptable salt thereof.

23. The compound of claim 13 of the formula:

or a pharmaceutically acceptable salt thereof.

24. The compound of claim 13 of the formula:

or a pharmaceutically acceptable salt thereof.

25. A pharmaceutical composition comprising a compound or pharmaceutically acceptable salt thereof of claim 1 optionally in a pharmaceutically acceptable carrier.

26. A pharmaceutical composition comprising a compound or pharmaceutically acceptable salt thereof of claim 13 optionally in a pharmaceutically acceptable carrier.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Nov 8, 2023
From: PERCEPTIVE CREDIT HOLDING III, LP
To: C4 THERAPEUTICS, INC.
Reel/Frame 065500/0944 →
SECURITY AGREEMENT Recorded Jun 9, 2020
From: C4 THERAPEUTICS, INC.
To: PERCEPTIVE CREDIT HOLDINGS III, LP
Reel/Frame 052874/0768 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2020
From: BRITSCHGI, ADRIAN; DEY, FABIAN; GOERGLER, ANNICK; KUSZNIR, ERIC ANDRE; NORCROSS, ROGER; WICHERT, MORENO ATTILIO
To: F. HOFFMAN-LA ROCHE AG
Reel/Frame 052636/0251 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2020
From: F. HOFFMAN-LA ROCHE AG
To: HOFFMAN-LA ROCHE INC.
Reel/Frame 052636/0256 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2020
From: HOFFMAN-LA ROCHE INC.
To: C4 THERAPEUTICS, INC.
Reel/Frame 052636/0264 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2020
From: F. HOFFMAN-LA ROCHE AG
To: C4 THERAPEUTICS, INC.
Reel/Frame 052636/0551 →
Priority Claims (1)
EP 17189229 · Sep 4, 2017 · regional
Continuity (2)
Continuation PCTEP2018073555 · Sep 3, 2018
Related Publication 20200207733A1 · Jul 2, 2020
Cited By (2)
US 12,441,740 US 12,559,492