IP Library Granted Patent US 11,673,902
Granted Patent B2
US 11,673,902 · App. 17/843,769 · Granted Jun 13, 2023

Isoindolinone and indazole compounds for the degradation of EGFR

Inventors: Christopher G. Nasveschuk (Stoneham, MA); Martin Duplessis (Somerville, MA); Jae Young Ahn (Somerville, MA); Alexander W. Hird (Belmont, MA); Ryan E. Michael (Erie, CO); Kiel Lazarski (Boston, MA); Yanke Liang (Belmont, MA); Georg Jaeschke (Basel, CH); Antonio Ricci (Biel-Benken, CH); Annick Goergler (Colmar, FR); Daniel Rueher (Raedersdorf, FR)
Assignee: C4 Therapeutics, Inc.
C07D519/00A61K9/009A61K9/02A61K9/08A61K9/2013A61K9/2018A61K9/2054A61K9/485A61K9/4825A61K9/4858A61K9/4866A61K47/10A61K47/12A61K47/26A61K47/32A61K47/38C07D487/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,673,902
App. No.
17/843,769
Granted
Jun 13, 2023
Kind
B2
Abstract

The invention provides compounds that degrade the epidermal growth factor receptor (EGFR) including mutant forms via the ubiquitination of the EGFR protein and subsequent proteasomal degradation. The compounds are useful for the treatment of various cancers.

Claims (42)

1. A compound of Formula:

or a pharmaceutically acceptable salt thereof;

wherein:

y is 0, 1, 2, or 3;

B* is heteroaryl or aryl optionally substituted with 1, 2, or 3 R 31 substituents;

R 31 is independently selected at each occurrence from the group consisting of hydrogen, F, Cl, Br, I, C 1-6 -alkyl, cyano, C 1-6 -alkoxy, halo-C 1-6 -alkoxy, halo-C 1-6 -alkyl, C 3-8 -cycloalkyl, and halo-C 3-8 -cycloalkyl and can be located on either ring where present on a bicycle;

R 32 is hydrogen, F, Cl, Br, I, C 1-6 -alkyl, halo-C 1-6 -alkyl, C 3-8 -cycloalkyl, or halo-C 3-8 -cycloalkyl; and

R 33 is hydrogen, F, Cl, Br, I, C 1-6 -alkyl, halo-C 1-6 -alkyl, C 3-8 -cycloalkyl, or halo-C 3-8 -cycloalkyl and can be located on the dihydropyrrole or imidazole ring.

2. The compound of claim 1 , wherein B* is

3. The compound of claim 2 , wherein y is 1.

4. The compound of claim 3 , wherein R 31 is selected from the group consisting of hydrogen, F, C 1-6 -alkyl, cyano, C 1-6 -alkoxy, and halo-C 1-6 -alkyl.

5. The compound of claim 3 , wherein R 31 is F.

6. The compound of claim 5 , wherein R 32 is hydrogen.

7. The compound of claim 6 , wherein R 33 is hydrogen.

8. The compound of claim 1 , wherein B* is

9. The compound of claim 8 , wherein R 31 is selected from the group consisting of hydrogen, F, C 1-6 -alkyl, cyano, C 1-6 -alkoxy, and halo-C 1-6 -alkyl.

10. The compound of claim 9 , wherein R 32 is hydrogen.

11. The compound of claim 10 , wherein R 33 is hydrogen.

12. The compound of claim 1 , wherein R 32 is hydrogen.

13. The compound of claim 12 , wherein B* is

14. The compound of claim 13 , wherein y is 1.

15. The compound of claim 1 , wherein R 33 is hydrogen.

16. The compound of claim 15 , wherein B* is

17. The compound of claim 16 , wherein y is 1.

18. The compound of claim 1 of structure:

or a pharmaceutically acceptable salt thereof.

19. A compound of structure:

or a pharmaceutically acceptable salt thereof.

20. The compound of claim 1 of structure:

or a pharmaceutically acceptable salt thereof.

21. A pharmaceutical composition comprising a compound of claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable excipient.

22. A pharmaceutical composition comprising a compound and a pharmaceutically acceptable excipient, wherein the compound is

or a pharmaceutically acceptable salt thereof.

23. The pharmaceutical composition of claim 22 , wherein the compound is of structure:

or a pharmaceutically acceptable salt thereof.

24. The pharmaceutical composition of claim 22 , wherein the compound is of structure:

or a pharmaceutically acceptable salt thereof.

25. The pharmaceutical composition of claim 24 , wherein the pharmaceutical composition is formulated for intravenous administration.

26. The pharmaceutical composition of claim 24 , wherein the pharmaceutical composition is formulated for oral administration.

27. The pharmaceutical composition of claim 26 , wherein the pharmaceutical composition is a tablet.

28. The pharmaceutical composition of claim 26 , wherein the pharmaceutical composition is a capsule.

29. The pharmaceutical composition of claim 24 , wherein the pharmaceutical composition is formulated for parenteral administration.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2025
From: NASVESCHUK, CHRISTOPHER G.; AHN, JAE YOUNG; DUPLESSIS, MARTIN; HIRD, ALEXANDER W.; MICHAEL, RYAN E.; LAZARSKI, KIEL; LIANG, YANKE
To: C4 THERAPEUTICS, INC.
Reel/Frame 070248/0636 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2025
From: JAESCHKE, GEORG; RICCI, ANTONIO; GOERGLER, ANNICK; RUEHER, DANIEL
To: F. HOFFMAN-LA ROCHE AG
Reel/Frame 070248/0647 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2025
From: F. HOFFMAN-LA ROCHE AG
To: HOFFMAN-LA ROCHE INC.
Reel/Frame 070248/0656 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 18, 2025
From: HOFFMAN-LA ROCHE INC.
To: C4 THERAPEUTICS, INC.
Reel/Frame 070248/0662 →
Continuity (4)
Continuation PCTUS2020066211 · Dec 18, 2020
Provisional Application 62951464 · Dec 20, 2019
Provisional Application 62951467 · Dec 20, 2019
Related Publication 20230110648A1 · Apr 13, 2023
Cited By (1)
US 12,441,740