IP Library Granted Patent US 11,530,223
Granted Patent B2
US 11,530,223 · App. 17/401,653 · Granted Dec 20, 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 11,530,223
App. No.
17/401,653
Granted
Dec 20, 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 (27)

1. A method of treating depression, Alzheimer's disease, attention deficit disorder, schizophrenia, anxiety, acute neuropathic pain, or chronic neuropathic pain in a patient in need thereof, the method comprising administering to the patient a therapeutically effective amount of 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 is 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 method of claim 1 , wherein R 1 is

3. The method of claim 1 , wherein R 1 is

4. The method of claim 1 , wherein R 3 is H.

5. The method 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 alkyl.

6. The method of claim 1 , wherein R 2 is H at each occurrence.

7. The method of claim 1 , wherein R 6 is absent.

8. The method of claim 1 , wherein R 7 is H at each occurrence.

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

10. The method of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt or a stereoisomer thereof.

11. The method of claim 1 , wherein the compound is selected from the group consisting of:

or a pharmaceutically acceptable salt or a stereoisomer thereof.

12. The method of claim 1 , wherein the neuropathic pain is selected from the group consisting of herpes, HIV, traumatic nerve injury, stroke, post-ischemia, chronic back pain, post-herpetic neuralgia, fibromyalgia, reflex sympathetic dystrophy, complex regional pain syndrome, spinal cord injury, sciatica, phantom limb pain, diabetic neuropathy, and cancer chemotherapeutic-induced neuropathic pain.

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 Aug 25, 2021
From: KHAN, M. AMIN
To: APTINYX INC.
Reel/Frame 057284/0499 →
Continuity (3)
Division 16321905
Provisional Application 62369453 · Aug 1, 2016
Related Publication 20220220119A1 · Jul 14, 2022