IP Library Granted Patent US 10,683,283
Granted Patent B2
US 10,683,283 · App. 16/329,984 · Granted Jun 16, 2020

Substituted ureas and methods of making and using same

Inventors: Brett A. Tounge (Blue Bell, PA); Shariff Bayoumy (North Wales, PA); Lawrence C. Kuo (Gwynedd Valley, PA); Scott Dax (Landenberg, PA)
Assignee: MEBIAS DISCOVERY, INC.
C07D409/12A61P29/00C07C273/18C07C275/06C07C275/14C07C275/26C07C275/28C07D207/09C07D209/44C07D215/08C07D215/14C07D215/18C07D333/20C07D333/22C07D405/12C07C2601/08C07C2601/10C07C2602/10
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Quick Facts
Patent No.
US 10,683,283
App. No.
16/329,984
Granted
Jun 16, 2020
Kind
B2
Abstract

The invention relates to substituted ureas, and compositions comprising the same, which in certain embodiments are useful for treating and/or preventing pain in a subject in need thereof.

Claims (78)

1. A compound of formula (I), or a salt, solvate, enantiomer, diastereoisomer, or tautomer thereof:

wherein:

A is selected from the group consisting of

B 1 is

and B 2 is H;

R 1 and R 2 are independently selected from the group consisting of H, CH 3 , and CH 3 substituted with at least one selected from the group consisting of fluoro, chloro, cyano, hydroxyl and nitro;

R 3 is selected from the group consisting of H and CH 3 ;

each occurrence of R is independently selected from the group consisting of fluoro, chloro, bromo, iodo, cyano, nitro, hydroxyl, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, phenyl, and substituted phenyl;

each occurrence of m is independently selected from the group consisting of 0, 1, 2 and 3;

n is selected from the group consisting of 1, 2 and 3; and

each occurrence of p is independently selected from the group consisting of 0, 1, 2 and 3.

2. The compound of claim 1 , wherein A is

3. The compound of claim 1 , wherein A is

4. The compound of claim 1 , wherein A is

5. The compound of claim 1 , wherein A is selected from the group consisting of isoindolin-2-yl, 5-fluoroisoindolin-2-yl, 5-chloroisoindolin-2-yl, 5-methoxyisoindolin-2-yl, 5-methylisoindolin-2-yl, 5-hydroxyisoindolin-2-yl, 5-cyanoisoindolin-2-yl, 4-fluoroisoindolin-2-yl, 4-chloroisoindolin-2-yl, 4-methoxyisoindolin-2-yl, 4-methylisoindolin-2-yl, 4-hydroxyisoindolin-2-yl, 4-cyanoisoindolin-2-yl, 5,6-difluoroisoindolin-2-yl, 5,6-dichloroisoindolin-2-yl, 6-chloro-5-fluoroisoindolin-2-yl, 5-chloro-6-fluoroisoindolin-2-yl, 1,2,3,4-tetrahydroquinolin-1-yl, 5-fluoro-1,2,3,4-tetrahydroquinolin-1-yl, 6-fluoro-1,2,3,4-tetrahydroquinolin-1-yl, 7-fluoro-1,2,3,4-tetrahydroquinolin-1-yl, 8-fluoro-1,2,3,4-tetrahydroquinolin-1-yl, 5-hydroxy-1,2,3,4-tetrahydroquinolin-1-yl, 6-hydroxy-1,2,3,4-tetrahydroquinolin-1-yl, 7-hydroxy-1,2,3,4-tetrahydroquinolin-1-yl, 8-hydroxy-1,2,3,4-tetrahydroquinolin-1l-yl, pyrrolidin-1-yl, and 3-phenyl-pyrrolidin-1-yl.

6. The compound of claim 1 , wherein B 1 is selected from the group consisting of 2-chloro-4-fluorophenyl, 4-chloro-2-fluorophenyl, 4-methoxyphenyl, 4-hydroxyphenyl, and phenyl.

7. A compound, or a salt, solvate, enantiomer, diastereoisomer or tautomer thereof, selected from the group consisting of:

N-(2-(2-Chloro-4-fluorophenyl)-2-(dimethylamino)ethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-(4-methoxyphenyl)ethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-(4-methoxyphenyl)ethyl)-5-fluoroisoindoline-2-carboxamide;

N-(2-(2-Chloro-4-fluorophenyl)-2-(dimethylamino)ethyl)-5-fluoroisoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-phenylethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-phenylethyl)-5-fluoroisoindoline-2-carboxamide;

(S)-3-Phenyl-pyrrolidine-1-carboxylic acid [2-dimethylamino-2-(4-methoxy-phenyl)-ethyl]-amide;

(R)-3-Phenyl-pyrrolidine-1-carboxylic acid [2-dimethylamino-2-(4-methoxy-phenyl)-ethyl]-amide;

(−)-N-(2-(Dimethylamino)-2-phenylethyl)isoindoline-2-carboxamide;

(−)-N-(2-(Dimethylamino)-2-phenylethyl)-isoindoline-2-carboxamide;

N-(2-Dimethylamino)-2-(4-methoxyphenyl)ethyl)-6-fluoro-3,4-dihydroquinoline-1(2H)-carboxamide;

N-(2-Dimethylamino)-2-phenylethyl)-3,4-dihydroquinoline-1(2H)-carboxamide;

N-(2-Dimethylamino)-2-phenylethyl)-6-fluoro-3,4-dihydroquinoline-1(2H)-carboxamide;

(−)-5-Fluoro-N-(2-(4-methoxyphenyl)-2-(methylamino)ethyl)isoindoline-2-carboxamide;

(+)-5-Fluoro-N-(2-(4-methoxyphenyl)-2-(methylamino)ethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-(4-hydroxyphenyl)ethyl)-5-fluoroisoindoline-2-carboxamide;

N-(2-(dimethylamino)-2-(4-hydroxyphenyl)ethyl)-5-hydroxyisoindoline-2-carboxamide;

N-(2-(Methylamino)-2-phenylethyl)isoindoline-2-carboxamide;

(−)-N-(2-(Methylamino)-2-phenylethyl)isoindoline-2-carboxamide; and

(+)-N-(2-(Methylamino)-2-phenylethyl)isoindoline-2-carboxamide.

8. A pharmaceutical composition comprising at least one pharmaceutically acceptable carrier and at least one compound of claim 1 .

9. A method of treating or ameliorating pain in a subject, the method comprising administering to the subject a therapeutically effective amount of at least one compound of formula (I), or a salt, solvate, enantiomer, diastereoisomer or tautomer thereof:

wherein:

A is selected from the group consisting of

B 1 is

and B 2 is H;

R 1 and R 2 are independently selected from the group consisting of H, CH 3 , and CH 3 substituted with at least one selected from the group consisting of fluoro, chloro, cyano, hydroxyl and nitro;

R 3 is selected from the group consisting of H and CH 3 ;

each occurrence of R is independently selected from the group consisting of fluoro, chloro, bromo, iodo, cyano, nitro, hydroxyl, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, phenyl, and substituted phenyl;

each occurrence of m is independently selected from the group consisting of 0, 1, 2 and 3;

n is selected from the group consisting of 1, 2 and 3; and

each occurrence of p is independently selected from the group consisting of 0, 1, 2 and 3.

10. A method of treating or ameliorating pain in a subject, the method comprising administering to the subject a therapeutically effective amount of at least one compound selected from the group of:

N-(2-(2-Chloro-4-fluorophenyl)-2-(dimethylamino)ethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-(4-methoxyphenyl)ethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-(4-methoxyphenyl)ethyl)-5-fluoroisoindoline-2-carboxamide;

N-(2-(2-Chloro-4-fluorophenyl)-2-(dimethylamino)ethyl)-5-fluoroisoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-phenylethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-phenylethyl)-5-fluoroisoindoline-2-carboxamide;

(S)-3-Phenyl-pyrrolidine-1-carboxylic acid [2-dimethylamino-2-(4-methoxy-phenyl)-ethyl]-amide;

(R)-3-Phenyl-pyrrolidine-1-carboxylic acid [2-dimethylamino-2-(4-methoxy-phenyl)-ethyl]-amide;

(−)-N-(2-(Dimethylamino)-2-phenylethyl)isoindoline-2-carboxamide;

(+)-N-(2-(Dimethylamino)-2-phenylethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-(4-methoxyphenyl)ethyl)-6-fluoro-3,4-dihydroquinoline-1(2H)-carboxamide;

N-(2-(Dimethylamino)-2-phenylethyl)-3,4-dihydroquinoline-1(2H)-carboxamide;

N-(2-(Dimethylamino)-2-phenylethyl)-6-fluoro-3,4-dihydroquinoline-1 (2H)-carboxamide;

(−)-5-Fluoro-N-(2-(4-methoxyphenyl)-2-(methylamino)ethyl)isoindoline-2-carboxamide;

(+)-5-Fluoro-N-(2-(4-methoxyphenyl)-2-(methylamino)ethyl)isoindoline-2-carboxamide;

N-(2-(Dimethylamino)-2-(4-hydroxyphenyl)ethyl)-5-fluoroisoindoline-2-carboxamide;

N-(2-(dimethylamino)-2-(4-hydroxyphenyl)ethyl)-5-hydroxyisoindoline-2-carboxamide;

N-(2-(Methylamino)-2-phenylethyl)isoindoline-2-carboxamide;

(−)-N-(2-(Methylamino)-2-phenylethyl)isoindoline-2-carboxamide; and

(+)-N-(2-(Methylamino)-2-phenylethyl)isoindoline-2-carboxamide.

11. The method of claim 9 , wherein the at least one compound is a MOR agonist.

12. The method of claim 9 , wherein the at least one compound decreases cyclic adenosine monophosphate (cAMP) levels in the subject.

13. The method of claim 9 , wherein the at least one compound does not significantly induce recruitment, binding to, or association with a β-arrestin.

14. The method of claim 9 , wherein the at least one compound does not significantly cause at least one side effect selected from the group consisting of tachyphylaxis, respiratory depression, constipation, nausea, emesis, withdrawal, dependence, and addiction.

15. The method of claim 9 , wherein the pain comprises at least one pain type selected from the group consisting of chronic pain, neuropathic pain, nociceptive pain, hyperalgesia, and allodynia.

16. The method of claim 10 , wherein the at least one compound does not significantly cause at least one side effect selected from the group consisting of tachyphylaxis, respiratory depression, constipation, nausea, emesis, withdrawal, dependence, and addiction.

17. The method of claim 10 , wherein the pain comprises at least one pain type selected from the group consisting of chronic pain, neuropathic pain, nociceptive pain, hyperalgesia, and allodynia.

18. A pharmaceutical composition comprising at least one pharmaceutically acceptable carrier and at least one compound of claim 7 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2019
From: TOUNGE, BRETT A.; BAYOUMY, SHARIFF; KUO, LAWRENCE C.
To: MEBIAS DISCOVERY LLC
Reel/Frame 049763/0463 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2019
From: DAX, SCOTT
To: MEBIAS DISCOVERY LLC
Reel/Frame 049763/0550 →
Continuity (2)
Provisional Application 62382530 · Sep 1, 2016
Related Publication 20190194178A1 · Jun 27, 2019