IP Library Granted Patent US 10,752,596
Granted Patent B2
US 10,752,596 · App. 16/150,989 · Granted Aug 25, 2020

Nitrogen-containing heteroaryl compound and pharmaceutical use thereof

Inventors: Hironobu Nagamori (Takatsuki, JP); Tatsuya Nishimaru (Takatsuki, JP); Masaki Takagi (Takatsuki, JP); Ikuo Mitani (Takatsuki, JP); Yuichi Nakagawa (Takatsuki, JP)
Assignee: JAPAN TOBACCO INC.
C07D241/12A61K31/4418A61K31/4433A61K31/472A61K31/497A61K31/4965A61P19/06A61P43/00C07D213/46C07D213/55C07D217/16C07D405/04C07D405/10
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Quick Facts
Patent No.
US 10,752,596
App. No.
16/150,989
Granted
Aug 25, 2020
Kind
B2
Abstract

The invention provides a compound having a GLUT9 inhibitory activity. The compound is of Formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof.

Claims (89)

1. A compound of Formula [I], or a pharmaceutically acceptable salt thereof:

wherein

═X— is ═C(R 5 )— or ═N—;

-L-COOH is

(1) —COOH,

(2) —C(R 71 )(R 72 )—COOH,

(3) —C(R 73 )(R 74 )—C(R 75 )(R 76 )—COOH, or

(4) —O—C(R 77 )(R 78 )—COOH;

n is 0, 1, or 2;

m is 0, 1, 2, or 3;

R 1 is each independently halogen or C 1-3 alkyl;

R 2 is

(1) halogen,

(2) hydroxy,

(3) cyano,

(4) C 1-6 alkyl optionally substituted with 1 to 3 substituents independently selected from the group consisting of cyano and C 1-3 alkoxy,

(5) halo C 1-6 alkyl,

(6) C 1-6 alkoxy,

(7) halo C 1-6 alkoxy,

(8) —COOR 21 wherein R 21 is hydrogen or C 1-3 alkyl,

(9) —CON(R 22 )(R 23 ) wherein R 22 and R 23 are each independently hydrogen or C 1-3 alkyl,

(10) C 3-6 cycloalkyl or

(11) a 4- to 6-membered saturated heterocyclic group containing 1 or 2 hetero atom as a ring atom in addition to the carbon atoms, wherein the hetero atom is independently selected from the group consisting of oxygen, nitrogen and sulfur atoms, and

R 3 is

(1) hydrogen,

(2) halogen,

(3) cyano,

(4) C 1-3 alkyl,

(5) halo C 1-3 alkyl,

(6) C 1-3 alkoxy, or

(7) —COOR 31 wherein R 31 is hydrogen or C 1-3 alkyl or

R 2 and R 3 , together with the carbon atoms that they are bonded to, form a 4- to 6-membered saturated heterocycle containing 1 or 2 hetero atom as a ring atom in addition to the carbon atoms, wherein the hetero atom is independently selected from the group consisting of oxygen, nitrogen and sulfur atoms;

R 4 is

(1) C 1-8 alkyl optionally substituted with 1 to 3 substituents independently selected from the following Group A,

(2) halo C 1-6 alkyl,

(3) CON(R 41 )(R 42 ) wherein R 41 and R 42 are each independently hydrogen or C 1-6 alkyl,

(4) C 3-6 cycloalkyl optionally substituted with 1 to 3 substituents independently selected from C 1-3 alkoxy, or

(5) a 4- to 6-membered saturated heterocyclic group containing 1 or 2 hetero atom as a ring atom in addition to the carbon atoms, wherein the hetero atom is independently selected from the group consisting of oxygen, nitrogen and sulfur atoms, and wherein the ring atom in the heterocyclic group bonded to

 is a carbon atom, and

Group A consists of

(a) hydroxy,

(b) C 1-3 alkoxy optionally substituted with one hydroxy or one C 1-3 alkoxy,

(c) halo C 1-3 alkoxy,

(d) C 3-6 cycloalkyl optionally substituted with one hydroxy, and

(e) phenyl, and

R 5 is hydrogen, halogen or C 1-3 alkyl or

R 4 and R 5 , together with the carbon atoms that they are bonded to, form C 3-6 cycloalkane;

R 6 are each independently halogen, hydroxy, C 1-3 alkyl or C 1-3 alkoxy; and

R 71 , R 72 , R 73 , R 74 , R 75 , R 76 , R 77 , and R 78 are each independently hydrogen or C 1-3 alkyl.

2. The compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein -L-COOH is —COOH.

3. The compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein n is 0 or 1.

4. The compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein m is 0 or 1.

5. The compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein R 3 is (1) hydrogen or (2) halogen.

6. The compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein

R 4 is

(1) C 1-8 alkyl optionally substituted with 1 to 3 substituents independently selected from the following Group A,

(2) halo C 1-6 alkyl, or

(3) CON(R 41 )(R 42 ) wherein R 41 and R 42 are each independently hydrogen or C 1-6 alkyl, and Group A consists of

(a) hydroxy,

(b) C 1-3 alkoxy optionally substituted with one hydroxy or one C 1-3 alkoxy,

(c) halo C 1-3 alkoxy,

(d) C 3-6 cycloalkyl optionally substituted with one hydroxy, and

(e) phenyl.

7. A compound of the following formula or a pharmaceutically acceptable salt thereof:

8. A compound of the following formula or a pharmaceutically acceptable salt thereof:

9. A compound of the following formula or a pharmaceutically acceptable salt thereof:

10. A compound of the following formula or a pharmaceutically acceptable salt thereof:

11. A compound of the following formula or a pharmaceutically acceptable salt thereof:

12. A compound of the following formula or a pharmaceutically acceptable salt thereof:

13. A compound of the following formula or a pharmaceutically acceptable salt thereof:

14. A compound of the following formula or a pharmaceutically acceptable salt thereof:

15. A compound of the following formula or a pharmaceutically acceptable salt thereof:

16. A compound of the following formula or a pharmaceutically acceptable salt thereof:

17. A compound of the following formula or a pharmaceutically acceptable salt thereof:

18. A pharmaceutical composition comprising the compound according to any one of claims 1 and 7 - 17 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

19. A method for the treatment or prophylaxis of a disease selected from the group consisting of hyperuricemia, gout, and chronic kidney disease in a mammal in need of such treatment or prophylaxis, which comprises administering a pharmaceutically effective amount of the compound according to any one of claims 1 and 7 - 17 or a pharmaceutically acceptable salt thereof to the mammal.

20. A compound of the following formula:

21. A compound of the following formula:

22. A compound of the following formula:

23. A compound of the following formula:

24. A compound of the following formula:

25. A compound of the following formula:

26. A compound of the following formula:

27. A compound of the following formula thereof:

28. A compound of the following formula:

29. A compound of the following formula:

30. A compound of the following formula:

31. A pharmaceutical composition comprising the compound according to any one of claims 20 - 30 and a pharmaceutically acceptable carrier.

32. A method for the treatment or prophylaxis of a disease selected from the group consisting of hyperuricemia, gout, and chronic kidney disease in a mammal in need of such treatment or prophylaxis, which comprises administering a pharmaceutically effective amount of the compound according to any one of claims 20 - 30 to the mammal.

Assignments (2)
CHANGE OF ADDRESS Recorded Apr 8, 2026
From: JAPAN TOBACCO INC.
To: JAPAN TOBACCO INC.
Reel/Frame 075366/0624 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2019
From: NAGAMORI, HIRONOBU; NISHIMARU, TATSUYA; TAKAGI, MASAKI; MITANI, IKUO; NAKAGAWA, YUICHI
To: JAPAN TOBACCO INC.
Reel/Frame 048266/0012 →
Priority Claims (1)
JP 2017-194005 · Oct 4, 2017 · national
Continuity (1)
Related Publication 20190152926A1 · May 23, 2019