IP Library › Granted Patent US 11,680,068
Granted Patent B2
US 11,680,068 · App. 17/738,278 · Granted Jun 20, 2023

Compounds useful as RET inhibitors

Inventors: Allan Jordan (Macclesfield, GB); Rebecca Newton (Macclesfield, GB); George Hynd (Harlow, GB); Jonathan Mark Sutton (Harlow, GB); Bohdan Waszkowycz (Manchester, GB)
Assignee: Cancer Research Technology Limited
C07D487/04
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Quick Facts
Patent No.
US 11,680,068
App. No.
17/738,278
Granted
Jun 20, 2023
Kind
B2
Abstract

The present invention relates to compounds of formula I that function as inhibitors of RET (rearranged during transfection) kinase enzyme activity: wherein HET, bonds a, b, c and d, X 1 , X 2 , X 3 , X 4 , R 2 , and R 3 are each as defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, as well as other diseases or conditions in which RET kinase activity is implicated.

Claims (38)

1. A compound of formula Id:

or a pharmaceutically acceptable salt thereof, wherein:

R 1 is a group of the formula:

-L-Y-Q

L is absent;

Y is absent; and

Q is (1-6C)alkyl or (3-10C)cycloalkyl; wherein Q is optionally substituted by one or more substituent groups independently selected from (1-4C)alkyl and OR c , wherein each R c is hydrogen;

X 4 is CR n ;

R n is hydrogen or halo;

R 2 is hydrogen; and

Q 3 is hydrogen, (1-6C)alkyl, (1-6C)alkoxy, (3-8C)cycloalkyl, or heteroaryl; wherein Q 3 is optionally substituted by one or more substituent groups independently selected from (1-4C)alkyl, halo, (1-4C)haloalkyl, and OR t , wherein each R t is hydrogen; or Q 3 is optionally substituted by a group of the formula:

-L 4 -L Q4 -Z 4

L 4 is absent or is (1-3C)alkylene;

L Q4 is absent or is 0; and

Z 4 is hydrogen, (1-6C)alkyl, or (3-8C)cycloalkyl.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

R 1 is (1-6C)alkyl or (3-6C)cycloalkyl optionally substituted by one or more groups independently selected from (1-4C)alkyl and OR c , wherein R c is hydrogen.

3. The compound of claim 2 , or a pharmaceutically acceptable salt thereof, wherein:

R 1 is (1-6C)alkyl.

4. The compound of claim 3 , or a pharmaceutically acceptable salt thereof, wherein:

R 1 is tert-butyl.

5. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

X 4 is CR C ; and

R n is hydrogen.

6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

Q 3 is hydrogen, (1-6C)alkyl, (1-6C)alkoxy, (3-8C)cycloalkyl, or heteroaryl; wherein Q 3 is optionally substituted by one or more substituent groups independently selected from (1-4C)alkyl, halo, (1-4C)haloalkyl, and OR t , wherein each R t is hydrogen; or Q 3 is optionally substituted by a group of the formula:

-L 4 -L Q4 -Z 4

L 4 is absent or is (1-2C)alkylene;

L Q4 is absent or is 0; and

Z 4 is hydrogen, (1-6C)alkyl, or (3-8C)cycloalkyl.

7. A compound, or a pharmaceutically acceptable salt thereof, which is:

8. A pharmaceutical formulation comprising the compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.

9. A method of treating a cancer in which RET kinase activity is implicated in a subject in need thereof, said method comprising administering a therapeutically effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof, to the subject.

10. The method of claim 9 , wherein the cancer is leukemia, lung cancer, colon cancer, breast cancer, ovarian cancer, prostate cancer, liver cancer, pancreatic cancer, brain cancer, skin cancer, medullary thyroid cancer, or non-small cell lung cancer.

11. The method of claim 9 , wherein the cancer is a malignant neoplasm, a malignant tumor, or a solid tumor.

12. The method of claim 9 , wherein the cancer comprises a RET mutation.

13. The method of claim 12 , wherein the RET mutation is a RET fusion translocation.

14. The method of claim 13 , wherein the RET fusion translocation is KIF5B-RET or CCDC6-RET.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2023
From: JORDAN, ALLAN; NEWTON, REBECCA; WASZKOWYCZ, BOHDAN
To: CANCER RESEARCH TECHNOLOGY LIMITED
Reel/Frame 063480/0862 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2023
From: CHARLES RIVER DISCOVERY RESEARCH SERVICES UK LIMITED
To: CANCER RESEARCH TECHNOLOGY LIMITED
Reel/Frame 063480/0891 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2023
From: HYND, GEORGE; SUTTON, JONATHAN MARK
To: CHARLES RIVER DISCOVERY RESEARCH SERVICES UK LIMITED
Reel/Frame 063499/0353 →
Priority Claims (1)
GB 1705971 · Apr 13, 2017 · national
Continuity (2)
Continuation 16604332
Related Publication 20220348585A1 · Nov 3, 2022