IP Library Granted Patent US 11,299,495
Granted Patent B2
US 11,299,495 · App. 16/321,905 · Granted Apr 12, 2022

Spiro-lactam NMDA receptor modulators and uses thereof

Inventor: M. Amin Khan (Evanston, IL)
Assignee: Aptinyx Inc.
C07D487/10A61P25/02A61P25/18A61P25/22A61P25/24A61P25/28C07D471/10
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Quick Facts
Patent No.
US 11,299,495
App. No.
16/321,905
Granted
Apr 12, 2022
Kind
B2
Abstract

Disclosed are compounds having potency in the modulation of NMDA receptor activity. Such compounds can be used in the treatment of conditions such as depression and related disorders. Orally delivered formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.

Claims (33)

1. A compound represented by:

or a pharmaceutically acceptable salt and/or a stereoisomer thereof, wherein:

R 1 is selected from the group consisting of C 1 -C 6 alkyl, phenyl,

wherein C 1 -C 6 alkyl substituted by one, two or three substituents each independently selected from —C(O)NR a R b , —NR a R b , hydroxyl, S(O) w —C 1 -C 3 alkyl, SH, phenyl and halogen, and wherein phenyl is substituted by one, two or three substituents independently selected for each occurrence from —C(O)—C 1 -C 3 alkyl, hydroxyl, —C(O)— C 1 -C 3 alkyl, methyl, CF 3 and halogen;

R 7 is independently selected from the group consisting of H, —C 1 -C 6 alkyl, —S(O) w —C 1- C 3 alkyl, and halogen;

R 9 is independently selected from the group consisting of H, —C 1 -C 6 alkyl, —S(O) w —C 1- C 3 alkyl, and halogen, or one R 7 and one R 9 taken together with the adjacent carbons to which they are attached form a 3-membered carbocyclic ring which can be optionally substituted by one or two substituents independently selected from the group consisting of halogen, hydroxyl, —C 1 -C 3 alkyl, —C 1 -C 3 alkoxy, —C(O)NR a R b , and —NR a R b ;

R 2 is independently selected for each occurrence from the group consisting of H, C 1- C 6 alkyl, —S(O) w —C 1 -C 3 alkyl, —NR a R b and halogen;

R 6 represents one or two optional substitutions each on one or more available ring carbons, and is independently selected for each occurrence from the group consisting of C 1- C 6 alkyl, —S(O) w —C 1- C 3 alkyl, —NR a R b and halogen;

w is 0, 1, or 2;

R 3 is selected from the group consisting of H, C 1 -C 6 alkyl, —C(O)R 31 and —C(O)OR 32 ;

R 31 and R 32 are each independently selected from the group consisting of H, C 1- C 6 alkyl, —C 3 -C 6 cycloalkyl, and phenyl; and

R a and R b are each independently for each occurrence selected from the group consisting of H, phenyl, and C 1 -C 3 alkyl, or R a and R b taken together with the nitrogen to which they are attached form a 4-6 membered heterocyclic ring;

wherein any aforementioned C 1 -C 6 alkyl of R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 31 and R 32 , independently for each occurrence, is optionally substituted by one, two or three substituents each independently selected from —C(O)NR a R b , —NR a R b , hydroxyl, S(O) w —C 1 -C 3 alkyl, SH, phenyl and halogen, and any aforementioned phenyl, independently for each occurrence, is optionally substituted by one, two or three substituents each independently selected from —C(O)—C 1 -C 3 alkyl, hydroxyl, methyl, CF 3 and halogen.

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

3. The compound of claim 1 , wherein R 3 is H.

4. The compound of claim 1 , wherein R 3 is selected from the group consisting of:

wherein R a and R b are each independently selected for each occurrence from the group consisting of hydrogen and —C 1 -C 3 .

5. The compound of claim 1 , wherein R 2 is H at each occurrence.

6. The compound of claim 1 , wherein R 7 is H at each occurrence.

7. The compound of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt and/or a stereoisomer thereof.

8. The compound of claim 1 , selected from the group consisting of:

or a pharmaceutically acceptable salt and/or a stereoisomer thereof.

9. The compound of claim 1 , wherein R 1 is —C(O)—C 1 -C 6 alkyl.

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

11. The compound of claim 1 , wherein R 1 is

12. The compound of claim 1 , wherein R 9 is H at each occurrence.

13. The compound of claim 1 , wherein R 6 is absent.

14. The compound of claim 1 , wherein each R 2 , R 7 and R 9 is H.

15. The compound of claim 14 , wherein R 6 is absent.

16. A pharmaceutical composition comprising a compound of claim 1 , and a pharmaceutically acceptable excipient.

17. A pharmaceutical composition comprising a compound of claim 7 , and a pharmaceutically acceptable excipient.

18. A pharmaceutical composition comprising a compound of claim 8 , and a pharmaceutically acceptable excipient.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 1, 2023
From: APTINYX INC.
To: TENACIA BIOTECHNOLOGY (HONG KONG) CO., LIMITED
Reel/Frame 065426/0673 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2019
From: KHAN, M. AMIN
To: APTINYX INC.
Reel/Frame 051356/0567 →
Continuity (2)
Provisional Application 62369453 · Aug 1, 2016
Related Publication 20190177334A1 · Jun 13, 2019