IP Library › Granted Patent US 11,964,942
Granted Patent B2
US 11,964,942 · App. 17/737,580 · Granted Apr 23, 2024

SSAO inhibitors and use thereof

Inventors: Zaifang Ren (Shanghai, CN); Xuefeng Sun (Shanghai, CN); Qing Xu (Shanghai, CN)
Assignee: Eccogene (Shanghai) Co., Ltd.
C07D211/46C07C317/32C07D211/32C07D307/14C07D309/06C07D319/12
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Quick Facts
Patent No.
US 11,964,942
App. No.
17/737,580
Granted
Apr 23, 2024
Kind
B2
Abstract

The application relates to a compound of Formula (I′) or (I): or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, which modulates the activity of SSAO, a pharmaceutical composition comprising a compound of Formula (I′) or (I), and a method of treating or preventing a disease in which SSAO plays a role.

Claims (47)

1. A compound of Formula (I)

or a pharmaceutically acceptable salt, solvate, stereoisomer, or tautomer thereof, wherein:

each X is independently Cl or F;

p is 0, 1, 2, or 3;

L is absent, —O—, (C 1 -C 4 ) alkylene, substituted (C 1 -C 4 ) alkylene, —O—(C 1 -C 4 ) alkylene, substituted —O—(C 1 -C 4 ) alkylene, (C 1 -C 4 ) alkylene-O—, or substituted (C 1 -C 4 ) alkylene-O—, wherein the substituted (C 1 -C 4 ) alkylene, substituted —O—(C 1 -C 4 ) alkylene, or substituted (C 1 -C 4 ) alkylene-O— is substituted with one or more L 1 ;

each L 1 is independently (C 1 -C 4 ) alkyl, F, or CF 3 ; or two L 1 , together with the atom to which they are attached, form a 3- to 5-membered cycloalkyl ring;

each R 1 is independently H, F, methyl, ethyl, or CF 3 ;

R 2 is (C 1 -C 4 ) alkyl substituted with one or more (C 1 -C 4 ) alkoxy, (C 1 -C 4 ) alkoxy, NR 3 C(O)R 4 , or C(O)NR 3 R 4 ; or

R 2 is

wherein R 2 is optionally substituted with one or more R 5 ;

R 3 is H, methyl, or ethyl;

R 4 is (C 1 -C 4 ) alkyl or (C 3 -C 10 ) cycloalkyl optionally substituted with one or more R 8 ; or

R 3 and R 4 , together with atom(s) to which they are attached, form a 3- to 6-membered ring optionally comprising one additional heteroatom selected from N and O and optionally substituted with one or more R 5 ;

each R 5 is independently (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy, hydroxy, cyano, oxo, C(O)R 7 , C(O)NR 7 R 7′ , NR 3 C(O)R 7 , NR 3 S(O) 2 R 4 , S(O) 2 R 4 , (C 1 -C 4 ) alkyl substituted with one or more hydroxy or R 6 , (C 3 -C 10 ) cycloalkyl optionally substituted with one or more hydroxy or R 6 , or heterocyclyl comprising one or two 3- to 6-membering rings and 1 to 3 heteroatoms selected from N and O and optionally substituted with one or more hydroxy or R 6 ; or two R 5 , together with the atom or atoms to which they are attached, form a 3- to 5-membered saturated or 5- or 6-membered aromatic ring optionally comprising 1 or 2 heteroatoms selected from N and O;

each R 6 is independently NR 3 C(O)R 7 or C(O)NR 3 R 7 ;

each R 7 is independently

OH, (C 1 -C 4 ) alkoxy, (C 1 -C 6 ) alkyl optionally substituted with one or more (C 1 -C 4 ) alkoxy, CF 3 , F, or (C 3 -C 10 ) cycloalkyl,

(C 3 -C 10 ) cycloalkyl optionally substituted with one or more R 8 , or

phenyl optionally substituted with one or more R 8 ;

each R 7′ is independently H, methyl, or ethyl; or

R 7 and R 7′ , together with the atom to which they are attached, form a 3- to 6-membered ring optionally comprising one additional heteroatom selected from N and O and optionally substituted with one or more R 8 ; or

R 3 and R 7 , together with atom(s) to which they are attached, form a 3- to 6-membered ring optionally comprising one additional heteroatom selected from N and O and optionally substituted with one or more R 8 ; and

each R 8 is independently (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy, CF 3 , OH, or F.

2. The compound of claim 1 , wherein X is F.

3. The compound of claim 1 , wherein p is 1.

4. The compound of claim 1 , wherein L is absent or (C 1 -C 4 ) alkylene.

5. The compound of claim 1 , wherein each L 1 is independently methyl or two L 1 , together with the atom to which they are attached, form a cyclopropyl ring.

6. The compound of claim 1 , wherein each R 1 is H or methyl.

7. The compound of claim 1 , wherein R 2 is (C 1 -C 4 ) alkyl substituted with one or more (C 1 -C 4 ) alkoxy, (C 1 -C 4 ) alkoxy, NR 3 C(O)R 4 , or C(O)NR 3 R 4 .

8. The compound of claim 7 , wherein R 3 and R 4 , together with atom(s) to which they are attached, form a 3- to 6-membered ring optionally comprising one additional heteroatom selected from N and O and optionally substituted with one or more R 5 .

9. The compound of claim 1 , wherein R 2 is

wherein R 2 is optionally substituted with one or more R 5 .

10. The compound of claim 1 , wherein R 2 is

wherein R 2 is optionally substituted with one or more R 5 .

11. The compound of claim 10 , wherein R 2 is

wherein R 2 is optionally substituted with one or more R 5 .

12. The compound of claim 1 , wherein R 2 is

wherein R 2 is optionally substituted with one or more R 5 .

13. The compound of claim 1 , wherein at least one R 5 is (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy, hydroxy, cyano, oxo, C(O)R 7 , C(O)NR 7 R 7′ , NR 3 C(O)R 7 , NR 3 S(O) 2 R 4 , S(O) 2 R 4 , or (C 1 -C 4 ) alkyl substituted with one or more hydroxy or R 6 .

14. The compound of claim 1 , wherein at least one R 5 is (C 3 -C 10 ) cycloalkyl optionally substituted with one or more hydroxy or R 6 , or heterocyclyl comprising one or two 3- to 6-membering rings and 1 to 3 heteroatoms selected from N and O and optionally substituted with one or more hydroxy or R 6 ; or two R 5 , together with the atom or atoms to which they are attached, form a 3- to 5-membered saturated or 5- or 6-membered aromatic ring optionally comprising 1 or 2 heteroatoms selected from N and O.

15. The compound of claim 1 , wherein at least one R 7 is (C 1 -C 4 ) alkoxy, (C 1 -C 6 ) alkyl optionally substituted with one or more (C 1 -C 4 ) alkoxy, CF 3 , F, or (C 3 -C 10 ) cycloalkyl.

16. The compound of claim 1 , wherein at least one R 7 is (C 3 -C 10 ) cycloalkyl or phenyl optionally substituted with one or more R 8 .

17. The compound of claim 1 , wherein R 7 and R 7′ , together with atom(s) to which they are attached, form a 3- to 6-membered ring optionally comprising one additional heteroatom selected from N and O and optionally substituted with one or more R 8 .

18. The compound of claim 1 , wherein R 3 and R 7 , together with atom(s) to which they are attached, form a 3- to 6-membered ring optionally comprising one additional heteroatom selected from N and O and optionally substituted with one or more R 8 .

19. The compound of claim 1 , wherein at least one R 8 is (C 1 -C 4 ) alkyl or (C 1 -C 4 ) alkoxy.

20. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt, solvate, stereoisomer, or tautomer thereof, and a pharmaceutically acceptable diluent, excipient or carrier.

21. A method of modulating SSAO or treating a SSAO-mediated disorder, comprising administering to a subject in need thereof, a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt, solvate, stereoisomer, or tautomer thereof, wherein the SSAO-mediated disorder is liver inflammation, liver fibrosis, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, or stroke.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2024
From: ECCOGENE (SHANGHAI) CO., LTD.
To: ECCOGENE INC.
Reel/Frame 067431/0279 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2022
From: REN, ZAIFANG; SUN, XUEFENG; XU, QING
To: ECCOGENE (SHANGHAI) CO., LTD.
Reel/Frame 059867/0090 →
Continuity (2)
Division 17082323 · Oct 28, 2020
Related Publication 20230026801A1 · Jan 26, 2023