IP Library Granted Patent US 11,912,679
Granted Patent B2
US 11,912,679 · App. 18/372,771 · Granted Feb 27, 2024

Aryl alkynamide derivatives

Inventors: Junko Maeda (Tokyo, JP); Ikumi Kuriwaki (Tokyo, JP); Kai Kitamura (Tokyo, JP); Yumi Yamashita (Tokyo, JP); Kenichi Kakefuda (Tokyo, JP); Akio Kamikawa (Tokyo, JP); Kenji Negoro (Tokyo, JP); Wataru Hamaguchi (Tokyo, JP); Ryushi Seo (Tokyo, JP); Jeffrey Ciavarri (Cambridge, MA)
Assignees: Astellas Pharma, Inc.; Mitobridge, Inc.
C07D295/16C07C233/22C07C233/69C07C233/81C07C235/42C07C237/42C07C311/13C07C311/46C07D205/04C07D207/12C07D207/16C07D207/273C07D209/08C07D211/48C07D211/62C07D213/56C07D213/75C07D231/12C07D231/40C07D239/26C07D279/12C07D295/155C07D295/195C07D305/08C07D307/22C07D309/14C07D333/48C07D401/06C07D403/06C07D403/10C07D405/10C07D487/10
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Quick Facts
Patent No.
US 11,912,679
App. No.
18/372,771
Granted
Feb 27, 2024
Kind
B2
Abstract

[Problem] A compound which is useful as a STING inhibitor is provided. [Means for Solution] The present inventors have found aryl alkynamide derivatives having an inhibitory action on STING. The aryl alkynamide derivatives of the present invention have an inhibitory action on STING and can be used as an agent for treating an autoimmune disease, a neurodegenerative disease, a type I interferonopathy and/or other STING-mediated disease.

Claims (41)

1. A compound of formula (I) or a salt thereof:

wherein,

Ring A is phenyl,

Ring B is formula (V):

X is CH or N,

R a1 , R a2 and R b1 are H,

R b2 is halogeno-C 1-6 alkyl,

R 1 is H,

R 2 is C 1-6 alkyl which is substituted by one or two R 3 ,

or, R 1 and R 2 are linked to each other to form azetidinyl, pyrrolidinyl, piperidinyl or thiomorpholinyl together with the nitrogen atom to which R 1 and R 2 are attached, wherein the azetidinyl, pyrrolidinyl, piperidinyl or thiomorpholinyl may be optionally substituted with one or two R 7 ,

each R 3 is independently —OH or —C(═O)—NH 2 , and

each R 7 is independently —C 1-6 alkylene-OH, —OH, —C(═O)—NH 2 , oxo or imino.

2. The compound or a salt thereof according to claim 1 , wherein the compound is a compound selected from the following group of:

N 2 -{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}-L-serinamide,

1-[(3R,4R)-3,4-dihydroxypyrrolidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one,

1-{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}piperidine-4-carboxamide,

1-[(3R,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one,

1-[3,3-bis(hydroxymethyl)azetidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one,

N-[(2R)-2,3-dihydroxypropyl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynamide,

N-[(2S)-2,3-dihydroxypropyl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynamide,

1-[(3S,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one,

(3R)-1-{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}pyrrolidine-3-carboxamide,

1-[(3R,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-[6-phenyl-5-(trifluoromethyl)pyridin-3-yl]prop-2-yn-1-one, and

1-imino-4-{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}-1λ 6 -thiomorpholin-1-one.

3. A pharmaceutical composition comprising the compound or a salt thereof according to claim 1 and one or more pharmaceutically acceptable excipients.

4. A method for therapeutic treatment of an autoimmune disease, a neurodegenerative disease, a type I interferonopathy and/or other STING-mediated disease comprising administering to a subject an effective amount of the compound or a salt thereof according to claim 1 .

5. The compound or a salt thereof according to claim 2 wherein the compound is N 2 -{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}-L-serinamide.

6. The compound or a salt thereof according to claim 2 , wherein the compound is 1-[(3R,4R)-3,4-dihydroxypyrrolidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one.

7. The compound or a salt thereof according to claim 2 , wherein the compound is 1-{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}piperidine-4-carboxamide.

8. The compound or a salt thereof according to claim 2 , wherein the compound is 1-[(3R,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one.

9. The compound or a salt thereof according to claim 2 , wherein the compound is 1-[3,3-bis(hydroxymethyl)azetidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one.

10. The compound or a salt thereof according to claim 2 , wherein the compound is N-[(2R)-2,3-dihydroxypropyl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynamide.

11. The compound or a salt thereof according to claim 2 , wherein the compound is N-[(2S)-2,3-dihydroxypropyl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynamide.

12. The compound or a salt thereof according to claim 2 , wherein the compound is 1-[(3S,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-yn-1-one.

13. The compound or a salt thereof according to claim 2 , wherein the compound is (3R)-1-{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}pyrrolidine-3-carboxamide.

14. The compound or a salt thereof according to claim 2 , wherein the compound is 1-[(3R,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-[6-phenyl-5-(trifluoromethyl)pyridin-3-yl]prop-2-yn-1-one.

15. The compound or a salt thereof according to claim 2 , wherein the compound is 1-imino-4-{3-[2-(trifluoromethyl)[1,1′-biphenyl]-4-yl]prop-2-ynoyl}-1λ 6 -thiomorpholin-1-one.

16. A pharmaceutical composition comprising the compound or a salt thereof according to claim 2 and one or more pharmaceutically acceptable excipients.

17. A method for therapeutic treatment of systemic lupus erythematosus and/or Sjogren's syndrome comprising administering to a subject an effective amount of the compound or a salt thereof according to claim 1 .

18. A method for therapeutic treatment of an autoimmune disease, a neurodegenerative disease, a type I interferonopathy and/or other STING-mediated disease comprising administering to a subject an effective amount of the compound or a salt thereof according to claim 2 .

19. A method for therapeutic treatment of systemic lupus erythematosus and/or Sjogren's syndrome comprising administering to a subject an effective amount of the compound or a salt thereof according to claim 2 .

Assignments (3)
CHANGE OF NAME Recorded Jul 10, 2024
From: MITOBRIDGE, INC.
To: ASTELLAS ENGINEERED SMALL MOLECULES US, INCORPORATED
Reel/Frame 068274/0806 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 26, 2023
From: MAEDA, JUNKO; KURIWAKI, IKUMI; KITAMURA, KAI; YAMASHITA, YUMI; KAKEFUDA, KENICHI; KAMIKAWA, AKIO; NEGORO, KENJI; HAMAGUCHI, WATARU; SEO, RYUSHI
To: ASTELLAS PHARMA, INC.
Reel/Frame 065028/0016 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 26, 2023
From: CIAVARRI, JEFFREY
To: MITOBRIDGE, INC.
Reel/Frame 065028/0078 →
Continuity (3)
Continuation PCTUS2023013924 · Feb 27, 2023
Provisional Application 63314783 · Feb 28, 2022
Related Publication 20240018113A1 · Jan 18, 2024