IP Library › Granted Patent US 10,017,498
Granted Patent B2
US 10,017,498 · App. 14/789,250 · Granted Jul 10, 2018

Compounds useful for treating AIDS

Inventors: Jamal Tazi (Clapiers, FR); Florence Mahuteau (Saint Remy les Chevreuses, FR); Romain Najman (L'Hay-les-Roses, FR); Didier Scherrer (Castelnau le Lez, FR); Noelie Campos (Le Cres, FR); Aude Garcel (Le Cres, FR)
Assignees: ABIVAX; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; INSTITUT CURIE; UNIVERSITE DE MONTPELLIER
C07D403/12A61K31/4709A61K31/4985C07D213/74C07D215/38C07D215/42C07D215/46C07D241/44C07D401/12
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Quick Facts
Patent No.
US 10,017,498
App. No.
14/789,250
Granted
Jul 10, 2018
Kind
B2
Abstract

A compound having the following formula or a pharmaceutically acceptable salt thereof: where: R independently represents a hydrogen atom, a halogen atom, a (C 1 -C 3 )alkyl group, a —NR 1 R 2 group, a (C 1 -C 3 )fluoroalkoxy group, a —NO 2 group, a phenoxy group, or a (C 1 -C 4 )alkoxy group, R 1 and R 2 are independently a hydrogen atom or a (C 1 -C 3 )alkyl group, R′ is a hydrogen atom, a halogen atom, a (C 1 -C 3 )alkyl group, or a (C 1 -C 4 )alkoxy group, R″ is a hydrogen atom or a (C 1 -C 4 )alkyl group, n is 1, 2, or 3, and n′ is 1 or 2.

Claims (80)

1. A compound having the following formula or a pharmaceutically acceptable salt thereof:

where:

R′ is a hydrogen atom, a halogen atom, a (C 1 -C 3 )alkyl group, or a (C 1 -C 4 )alkoxy group,

R″ is a hydrogen atom or a (C 1 -C 4 )alkyl group,

n is 1 or 2, and

n′ is 1 or 2;

when n is 1, then R is a (C 1 -C 3 ) fluoroalkoxy group, a NR 1 R 2 group or a phenoxy group, where

R 1 and R 2 are independently a (C 1 -C 3 )group; and

when n is 2, then one of the two R is a (C 1 -C 3 ) fluoroalkoxy group and the other R is a (C 1 -C 3 )alkyl group.

2. A compound having the following formula or a pharmaceutically acceptable salt thereof:

where:

R independently represents a hydrogen atom, a halogen atom, a (C 1 -C 3 )alkyl group, a —NR 1 R 2 group, a (C 1 -C 3 )fluoroalkoxy group, a —NO 2 group, a phenoxy group, or a (C 1 -C 4 )alkoxy group,

R 1 and R 2 are independently a hydrogen atom or a (C 1 -C 3 )alkyl group,

R′ is a hydrogen atom, a halogen atom, a (C 1 -C 3 )alkyl group, or a (C 1 -C 4 )alkoxy group, with the proviso that R′ is different from a methyl group at position 4 of the quinoline group,

R″ is a hydrogen atom or a (C 1 -C 4 )alkyl group,

n is 1, 2, or 3, and

n′ is 1 or 2.

3. A compound having the following formula or a pharmaceutically acceptable salt thereof:

where:

R independently represents a hydrogen atom, a halogen atom, a (C 1 -C 3 )alkyl group, a —NR 1 R 2 group, a (C 1 -C 3 )fluoroalkoxy group, a —NO 2 group, a phenoxy group, or a (C 1 -C 4 )alkoxy group,

R 1 and R 2 are independently a hydrogen atom or a (C 1 -C 3 )alkyl group,

R″ is a hydrogen atom or a (C 1 -C 4 )alkyl group,

n is 1, 2, or 3, and

n′ is 1 or 2,

with the proviso that when n is 1, R is not a hydrogen atom, a methyl group in para of the bond linked to NR″, an ethoxy group in para of the bond linked to NR″, nor a fluorine atom in para of the bond linked to NR″.

4. A compound selected from the group consisting of:

(8) Quinolin-2-yl-(4-trifluoromethoxy-phenyl)-amine,

(75) 4-N-(8-chloroquinolin-2-yl)-1-N,1-N-dimethylbenzene-1,4-diamine,

(77) 8-chloro-N-(4-methoxyphenyl)quinolin-2-amine,

(78) 4-methyl-N-[4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(79) N-(4-methoxyphenyl)-3-methylquinolin-2-amine,

(80) 3-methyl-N-[4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(81) 1-N,1-N-dimethyl-4-N-(3-methylquinolin-2-yl)benzene-1,4-diamine,

(82) N-[2-methyl-4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(83) N-[3-(trifluoromethoxy)phenyl]quinolin-2-amine,

(84) N-[2-(trifluoromethoxy)phenyl]quinolin-2-amine,

(86) N-(3-fluorophenyl)quinolin-2-amine,

(87) 8-chloro-N-[3-(trifluoromethoxy)phenyl]quinolin-2-amine,

(88) 8-chloro-N-(3-fluorophenyl)quinolin-2-amine,

(89) N-(4-(trifluoromethoxy)phenyl)quinolin-2-amine

(90) 8-chloro-N-[4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(91) 3-methyl-N-[2-methyl-4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(92) 3-methyl-N-[3-(trifluoromethoxy)phenyl]quinolin-2-amine,

(93) 3-methyl-N-[2-(trifluoromethoxy)phenyl]quinolin-2-amine,

(94) 8-chloro-N-[2-methyl-4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(95) 3-methyl-N-(4-(trifluoromethoxy)phenyl)quinolin-2-amine

(96) 6-chloro-N-(4-(trifluoromethoxy)phenyl)quinolin-2-amine,

(97) 4-methyl-N-(4-(trifluoromethoxy)phenyl)quinolin-2-amine

(98) 8-bromo-N-[4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(99) 8-fluoro-N-[4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(100) 8-methyl-N-[4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(101) N-(4-butoxyphenyl)-8-chloroquinolin-2-amine,

(102) N-(4-phenoxyphenyl)quinolin-2-amine,

(103) 8-methoxy-N-[4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(104) 8-chloro-N-[3-chloro-4-(trifluoromethoxy)phenyl]quinolin-2-amine,

(155) N-(4-butoxyphenyl)-3-methylquinolin-2-amine,

(156) 4-N-(6-chloroquinolin-2-yl)-1-N,1-N-dimethylbenzene-1,4-diamine,

(157) 8-chloro-N-(3-chloro-4-methoxyphenyl)quinolin-2-amine,

(158) N1-(8-chloroquinolin-2-yl)-4-(trifluoromethoxy)benzene-1,2-diamine, and

their pharmaceutically acceptable salts.

5. The compound of claim 4 , wherein the pharmaceutically acceptable salts are selected from hydrobromide, tartrate, citrate, trifluoroacetate, ascorbate, hydrochloride, triflate, maleate, mesylate, formate, acetate, and fumarate.

6. A pharmaceutical composition comprising at least one compound as defined in claim 1 .

7. A pharmaceutical composition comprising at least one compound as defined in claim 2 .

8. A pharmaceutical composition comprising at least one compound as defined in claim 3 .

9. A pharmaceutical composition comprising at least one compound as defined in claim 4 .

10. A pharmaceutical composition comprising at least one compound as defined in claim 5 .

11. The pharmaceutical composition according to claim 6 , further comprising a pharmaceutically acceptable support.

12. The pharmaceutical composition according to claim 7 , further comprising a pharmaceutically acceptable support.

13. The pharmaceutical composition according to claim 8 , further comprising a pharmaceutically acceptable support.

14. The pharmaceutical composition according to claim 9 , further comprising a pharmaceutically acceptable support.

15. The pharmaceutical composition according to claim 10 , further comprising a pharmaceutically acceptable support.

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

where:

R independently represents a (C 1 -C 3 )fluoroalkoxy group,

R′ is a hydrogen atom, a halogen atom, a (C 1 -C 3 )alkyl group or a (C 1 -C 4 )alkoxy group,

R″ is a hydrogen atom or a (C 1 -C 4 )alkyl group,

n is 1, and

n′ is 1 or 2.

17. A pharmaceutical composition comprising at least one compound as defined in claim 16 .

18. The pharmaceutical composition according to claim 16 , further comprising a pharmaceutically acceptable support.

Assignments (1)
MERGER AND CHANGE OF NAME Recorded Dec 1, 2015
From: UNIVERSITE DE MONTPELLIER 2; UNIVERSITE MONTPELLIER 2
To: UNIVERSITE DE MONTPELLIER
Reel/Frame 037179/0237 →
Priority Claims (2)
EP 09162630 · Jun 12, 2009 · regional
EP 09305540 · Jun 12, 2009 · regional
Continuity (4)
Continuation 13377760
Provisional Application 61186552 · Jun 12, 2009
Provisional Application 61186544 · Jun 12, 2009
Related Publication 20150307478A1 · Oct 29, 2015
Cited By (1)
US 12,202,804