IP Library Granted Patent US 12,162,882
Granted Patent B2
US 12,162,882 · App. 18/217,002 · Granted Dec 10, 2024

Quinolone derivatives as fibroblast growth factor receptor inhibitors

Inventors: Erik Verner (Belmont, CA); Kenneth Albert Brameld (Menlo Park, CA)
Assignee: PRINCIPIA BIOPHARMAC, INC.
C07D471/04A61K31/519A61K31/5377A61K45/06C07D487/04C07D519/00
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Quick Facts
Patent No.
US 12,162,882
App. No.
18/217,002
Granted
Dec 10, 2024
Kind
B2
Abstract

Compounds that are Fibroblast Growth Factor Inhibitors (FGFR) and are therefore useful for the treatment of diseases treatable by inhibition of FGFR are disclosed. Also disclosed are pharmaceutical compositions containing such compounds and processes for preparing such compounds.

Claims (31)

1. A method of treating a disease in a patient, the method comprising administering a compound of Formula (III):

wherein:

J is N;

J′ is CH;

Ar is phenyl substituted with one, two, three, or four substituents independently selected from alkoxy and halo;

R 2 is hydrogen or alkyl; and

Q is alkylene; and

X is a group of formula (a):

wherein:

each R 3 is hydrogen or alkyl; and

each R 4 is hydrogen or alkyl;

Y is —CO—;

R c is hydrogen or alkyl; and

R d is hydrogen or alkyl;

or a pharmaceutically acceptable salt thereof;

wherein the disease is chosen from skeletal dysplasia, craniosynostosis, and dwarf syndromes.

2. The method of claim 1 , wherein Q is n-propylene.

3. The method of claim 1 , wherein R 2 is alkyl.

4. The method of claim 1 , wherein R 2 is hydrogen.

5. The method of claim 1 , wherein Ar is 3-methoxyphenyl, 2-halo-3-methoxyphenyl, 2-halo-5-methoxyphenyl, 2-halo-3,5-dimethoxyphenyl, 2,6-dihalo-3,5-dimethoxyphenyl, 3,5-dimethoxyphenyl, 2-halophenyl, or 2,6-dihalophenyl.

6. The method of claim 1 , wherein Ar is 2-chloro-3,5-dimethoxy-phenyl, 3,5-dimethoxyphenyl, 2-chlorophenyl, or 2,6-dichloro-3,5-dimethoxyphenyl.

7. The method of claim 1 , wherein R c and R d are hydrogen.

8. The method of any of the claims 1, 2, 3, 4, 5, 6 and 7 or a pharmaceutically acceptable salt thereof wherein R c is alkyl and R d is hydrogen.

9. The method of claim 1 , wherein the compound of Formula (III) is selected from:

8-(3-(4-acryloylpiperazin-1-yl) propyl)-2-amino-6-(2,6-dichloro-3,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidin-7 (8H)-one; or

8-(3-(4-acryloylpiperazin-1-yl) propyl)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7 (8H)-one;

and a pharmaceutically acceptable salt thereof.

10. The method of claim 1 , wherein the compound of Formula (III) is selected from:

8-(3-(4-acryloylpiperazin-1-yl) propyl)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7 (8H)-one;

and a pharmaceutically acceptable salt thereof.

11. The method of claim 1 , wherein the skeletal dysplasia is chosen from achondroplasia, hypochondroplasia, thanatophoric dysplasia, and platyspondylic lethal skeletal dysplasia.

Assignments (2)
ASSIGNEE CHANGE OF ADDRESS Recorded Sep 16, 2025
From: PRINCIPIA BIOPHARMA INC.
To: PRINCIPIA BIOPHARMA INC.
Reel/Frame 072881/0270 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2024
From: VERNER, ERIK; BRAMELD, KENNETH ALBERT
To: PRINCIPIA BIOPHARMA, INC.
Reel/Frame 067051/0122 →
Continuity (8)
Continuation 17306528 · May 3, 2021
Continuation 16383237 · Apr 12, 2019
Continuation 15806525 · Nov 8, 2017
Continuation 15022869
Provisional Application 62069932 · Oct 29, 2014
Provisional Application 62007562 · Jun 4, 2014
Provisional Application 61937211 · Feb 7, 2014
Related Publication 20240092777A1 · Mar 21, 2024