Ghrelin O-acyltransferase inhibitors

Patent metadata

Field	Value
Publication number	US-11312709-B2
Application number	US-201916967262-A
Country	US
Kind code	B2
Filing date	Feb 5, 2019
Priority date	Feb 5, 2018
Publication date	Apr 26, 2022
Grant date	Apr 26, 2022

Abstract

This invention relates to novel compounds according to Formula (I) which are inhibitors of ghrelin O-acyltransferase (GOAT), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the treatment of metabolic disorders (e.g. Prader-Willi syndrome, metabolic syndrome, insulin resistance, impaired glucose tolerance, prediabetes, diabetes mellitus (e.g., type II diabetes mellitus), dysglycemia (e.g., hyperglycemia), obesity (e.g., obesity caused by Prader-Willi syndrome), increased adiposity, poor glycemic control, hyperphagia, impaired satiety, dyslipidemia (e.g., atherogenic dyslipidemia), hepatic steatosis (e.g., non-alcoholic fatty liver disease (e.g., non-alcoholic steatohepatitis))), psychiatric disorders (e.g., eating disorders (e.g., bulimia nervosa, binge eating disorder, night-time eating syndrome), substance related disorders (e.g., addiction disorders (e.g., alcohol, smoking, overeating, or use of illicit drugs))), as well as disorders related to or complications of metabolic or psychiatric disorders (e.g., cardiovascular diseases (e.g., diabetic heart disease (e.g., diabetic cardiomyopathy), heart failure, or hypertension), ischemia (e.g., myocardial ischemia, cerebral ischemia, ischemic stroke), or BMI-related cancers (e.g., pancreatic cancer, gallbladder cancer, esophageal cancer, colorectal cancer, breast cancer etc.).

First claim

What is claimed is:

1. A compound according to Formula (I) or a pharmaceutically acceptable salt thereof:

wherein:
R 1 is hydrogen, halogen, cyano, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, or C(═O)NH 2 ;
X is CH 2 or O;
R 2 is halogen; and
R 3 is hydrogen or halogen.

2. The compound or pharmaceutically acceptable salt thereof according to claim 1 , represented by Formula (II):

wherein:
R 1 is hydrogen, halogen, cyano, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, or C(═O)NH 2 ;
X is CH 2 or O;
R 2 is halogen; and
R 3 is hydrogen or halogen.

3. The compound or pharmaceutically acceptable salt thereof according to claim 1 , represented by Formula (III):

wherein:
R 1 is hydrogen, halogen, cyano, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, or —C(═O)NH 2 ;
X is CH 2 or O;
R 2 is halogen; and
R 3 is hydrogen or halogen.

4. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 1 is hydrogen, chloro, cyano, methyl, —CF 3 , or —C(═O)NH 2 .

5. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 1 is hydrogen.

6. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein X is CH 2 .

7. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein X is O.

8. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 2 is chloro.

9. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 3 is hydrogen, chloro, or fluoro.

10. The compound or pharmaceutically acceptable salt thereof according to claim 1 , wherein R 3 is hydrogen.

11. The compound according to claim 1 which is:
2-(4-chloro-6-((6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4-chloro-6-((6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4-chloro-6-((6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(4-chloro-6-((2-methyl-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4-chloro-6-((2-methyl-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4-chloro-6-((2-methyl-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(4,7-dichloro-6-((2-chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4,7-dichloro-6-((2-chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4,7-dichloro-6-((2-chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(4,7-dichloro-6-((2-(trifluoromethyl)-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4,7-dichloro-6-((2-(trifluoromethyl)-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4,7-dichloro-6-((2-(trifluoromethyl)-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(4-chloro-7-fluoro-6-((6-(trifluoromethyl)-2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4-chloro-7-fluoro-6-((6-(trifluoromethyl)-2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4-chloro-7-fluoro-6-((6-(trifluoromethyl)-2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(4-chloro-6-((2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4-chloro-6-((2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4-chloro-6-((2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(4,7-dichloro-6-((2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4,7-dichloro-6-((2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4,7-dichloro-6-((2,3-dihydrofuro[2,3-b]pyridin-3-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(4-chloro-6-((2-cyano-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(R)-2-(4-chloro-6-((2-cyano-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
(S)-2-(4-chloro-6-((2-cyano-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)benzo[b]thiophen-3-yl)acetic acid;
2-(6-((2-carbamoyl-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)-4-chlorobenzo[b]thiophen-3-yl)acetic acid;
(R)-2-(6-((2-carbamoyl-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)-4-chlorobenzo[b]thiophen-3-yl)acetic acid; or
(S)-2-(6-((2-carbamoyl-6,7-dihydro-5H-cyclopenta[b]pyridin-5-yl)oxy)-4-chlorobenzo[b]thiophen-3-yl)acetic acid;
or a pharmaceutically acceptable salt thereof.

12. The compound according to claim 1 which is:

or a pharmaceutically acceptable salt thereof.

13. The compound according to claim 1 which is:

or a pharmaceutically acceptable salt thereof.

14. The compound according to claim 13 which is:

15. A combination of a compound or pharmaceutically acceptable salt thereof according claim 1 and at least one anti-adiposity agent or anti-adiposity therapy.

16. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to claim 1 and a pharmaceutically acceptable excipient.

17. The pharmaceutical composition of claim 16 , further comprising an additional pharmaceutical agent.

18. A method of treating Prader-Willi syndrome, metabolic syndrome, insulin resistance, impaired glucose tolerance, prediabetes, diabetes mellitus, type 2 diabetes mellitus, dysglycemia, hyperglycemia, obesity, increased adiposity, poor glycemic control, hyperphagia, impaired satiety, dyslipidemia, atherogenic dyslipidemia, hepatic steatosis, non-alcoholic fatty liver disease, or non-alcoholic steatohepatitis in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.

19. A method of treating obesity in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.

20. A method of treating Prader-Willi syndrome in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.

Assignees

• Glaxosmithkline Ip Dev Ltd

Inventors

• Bandyopadhyay Anish
• Cheung Mui
• Eidam Hilary Schenck
• Joshi Hemant
• Su Dai-Shi

Classifications

• C07D491/048

  the oxygen-containing ring being five-membered · CPC title

• C07D409/12 Primary

  linked by a chain containing hetero atoms as chain links · CPC title

• A61K31/4436

  containing a heterocyclic ring having sulfur as a ring hetero atom · CPC title

• A61K31/4355

  the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom · CPC title

• A61K45/06

  Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title