IP Library Granted Patent US 7,326,790
Granted Patent B2
US 7,326,790 · App. 10/836,561 · Granted Feb 5, 2008

Diphenylisoxazole compounds and hydro isomers thereof

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Quick Facts
Patent No.
US 7,326,790
App. No.
10/836,561
Granted
Feb 5, 2008
Kind
B2
Abstract

The present invention relates to substituted diphenylisoxazole compounds and pharmaceutical compositions thereof that inhibit replication of HCV virus. The present invention also relates to the use of compounds and/or compositions to inhibit HCV replication and/or proliferation and to treat or prevent HCV infections.

Claims (61)

1. A compound of the formula,

or a pharmaceutically acceptable salt, hydrate, solvate, N-oxide or prodrug thereof, wherein:

one of X and Y is O and the other is N or N(R 16 );

ring B is an isoxazolyl, isoxazolinyl, or isoxazolidinyl ring;

R 2 , R 3 , R 4 , R 5 , R 6 , R 9 , R 10 , R 20 , R 30 , and R 40 are each, independently of one another, selected from the group consisting of hydrogen, —OH, —SH, —CN, —NO 2 , —N 3 , halo, fluoro, chloro, bromo, iodo, lower alkyl, substituted lower alkyl, lower heteroalkyl, substituted lower heteroalkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, lower haloalkyl, monohalomethyl, dihalomethyl, trihalomethyl, trifluoromethyl, lower alkylthio, substituted lower alkylthio, lower alkoxy, substituted lower alkoxy, methoxy, substituted methoxy, lower heteroalkoxy, substituted lower heteroalkoxy, cycloalkoxy, substituted cycloalkoxy, cycloheteroalkoxy, substituted cycloheteroalkoxy, lower haloalkoxy, monohalomethoxy, dihalomethoxy, trihalomethoxy, trifluoromethoxy, amino, lower di- or monoalkylamino, substituted lower di- or monoalkylamino, aryl, substituted aryl, aryloxy, substituted aryloxy, phenoxy, substituted phenoxy, arylalkyl, substituted arylalkyl, arylalkyloxy, substituted arylalkyloxy, benzyl, benzyloxy, heteroaryl, substituted heteroaryl, heteroaryloxy, substituted heteroaryloxy, heteroarylalkyl, substituted heteroarylalkyl, heteroarylalkyloxy, substituted heteroarylalkyloxy, carboxyl, lower alkoxycarbonyl, substituted lower alkoxycarbonyl, aryloxycarbonyl, substituted aryloxycarbonyl, arylalkyloxycarbonyl, substituted arylalkyloxycarbonyl, carbamate, substituted carbamate, carbamoyl, substituted carbamoyl, sulfamoyl, substituted sulfamoyl and a group of the formula -L-R 14 , where “L” is a linker and R 14 is cycloalkyl, substituted cycloalkyl, cycloheteroalkyl or substituted cycloheteroalkyl,

provided that one and only one of R 20 , R 30 , and R 40 is —N(R 11 )C(O)R 12 ; and

provided that when ring B is isoxazolyl, then R 30 is not —N(R 11 )C(O)R 12 ;

R 11 is hydrogen or lower alkyl;

R 12 is monohalomethyl or dihalomethyl; and

R 16 is selected from the group consisting of hydrogen, lower alkyl, substituted lower alkyl, lower heteroalkyl, substituted lower heteroalkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, lower haloalkyl, monohalomethyl, dihalomethyl, trihalomethyl, trifluoromethyl, lower alkylthio, substituted lower alkylthio, lower alkoxy, substituted lower alkoxy, methoxy, substituted methoxy, lower heteroalkoxy, substituted lower heteroalkoxy, cycloalkoxy, substituted cycloalkoxy, cycloheteroalkoxy, substituted cycloheteroalkoxy, lower haloalkoxy, monohalomethoxy, dihalomethoxy, trihalomethoxy, trifluoromethoxy, lower di- or monoalkylamino, substituted lower di- or monoalkylamino, aryl, substituted aryl, aryloxy, substituted aryloxy, phenoxy, substituted phenoxy, arylalkyl, substituted arylalkyl, arylalkyloxy, substituted arylalkyloxy, benzyl, benzyloxy, heteroaryl, substituted heteroaryl, heteroaryloxy, substituted heteroaryloxy, heteroarylalkyl, substituted heteroarylalkyl, heteroarylalkyloxy, substituted heteroarylalkyloxy, carboxyl, lower alkoxycarbonyl, substituted lower alkoxycarbonyl, aryloxycarbonyl, substituted aryloxycarbonyl, arylalkyloxycarbonyl, substituted arylalkyloxycarbonyl, carbamate, substituted carbamate, carbamoyl, substituted carbamoyl, sulfamoyl, substituted sulfamoyl and a group of the formula -L-R 14 , where “L” is a linker and R 14 is cycloalkyl, substituted cycloalkyl, cycloheteroalkyl or substituted cycloheteroalkyl.

2. The compound of claim 1 , of one of the formulas,

3. The compound of claim 2 , of one of the formulas,

4. The compound of claim 2 , of one of the formulas,

5. The compound of claim 2 , of one of the formulas,

6. The compound of claim 1 , of one of the formulas,

7. The compound of claim 6 , of one of the formulas,

8. The compound of claim 6 , of one of the formulas,

9. The compound of claim 6 , of one of the formulas,

10. The compound of claim 1 , of one of the formulas,

11. The compound of claim 10 , of one of the formulas,

12. The compound of claim 10 , of one of the formulas,

13. The compound of claim 10 , of one of the formulas,

14. The compound of claim 1 , of one of the formulas,

15. The compound of claim 14 , of one of the formulas,

16. The compound of claim 14 , of one of the formulas,

17. The compound of claim 14 , of one of the formulas,

18. The compound of claim 1 , of one of the formulas,

19. The compound of claim 18 , of one of the formulas,

20. The compound of claim 18 , of one of the formulas,

21. The compound of claim 1 which is,

2,2-Dichloro-N-[2-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamide;

2,2-Dichloro-N-[4-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamide;

(±)-2,2-Dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(2-isoxazolinyl)]phenyl]acetamide;

(±)-2,2-Dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolinyl)]phenyl]acetamide;

(R)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolinyl)]phenyl]acetamide;

(S)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolinyl)]phenyl]acetamide;

(±)-2,2-Dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(4-isoxazolinyl)]phenyl]acetamide;

(R)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(4-isoxazolinyl)]phenyl]acetamide;

(S)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(4-isoxazolinyl)]phenyl]acetamide;

(±)-2,2-Dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(3-isoxazolinyl)]phenyl]acetamide;

(R)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(3-isoxazolinyl)]phenyl]acetamide;

(S)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(3-isoxazolinyl)]phenyl]acetamide;

cis-(±)-2,2-Dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolidinyl)]phenyl]acetamide;

trans-(±)-2,2-Dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolidinyl)]phenyl]acetamide;

cis-(3S,5R)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolidinyl)]phenyl]acetamide;

cis-(3R,5S)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolidinyl)]phenyl]acetamide;

trans-(3S,5S)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolidinyl)]phenyl]acetamide;

trans-(3R,5R)-2,2-dichloro-N-[3-[3-(2,6-dichlorophenyl)-5-(2-isoxazolidinyl)]phenyl]acetamide;

cis-(±)-(±)-2,2-Dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(2-isoxazolidinyl)]phenyl]acetamide;

trans-(±)-2,2-Dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(2-isoxazolidinyl)]phenyl]acetamide;

cis-(3R,5S)-2,2-dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(2-isoxazolidinyl)]phenyl]acetamide;

cis-(3S,5R)-2,2-dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(2-isoxazolidinyl)]phenyl]acetamide;

trans-(3S,5S)-2,2-dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(2-isoxazolidinyl)]phenyl]acetamide;

trans-(3R,5R)-2,2-dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(2-isoxazolidinyl)]phenyl]acetamide;

2,2-Dichloro-N-[4-[3-(2-chlorophenyl)-5-isoxazolyl]phenyl]acetamide;

2,2-Dichloro-N-[4-[3-(2,6-difluorophenyl)-5-isoxazolyl]phenyl]acetamide;

2,2-Dichloro-N-[2-[3-(2,6-dichlorophenyl)-5-isoxazolyl]phenyl]acetamide;

2,2-Dichloro-N-[4-[5-(2,6-dichlorophenyl)-3-isoxazolyl]phenyl]acetamide;

(±)-2,2-Dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(4-isoxazolinyl)]phenyl]acetamide;

(±)-2,2-Dichloro-N-[3-[5-(2,6-dichlorophenyl)-3-(3-isoxazolinyl)]phenyl]acetamide;

or a pharmaceutically acceptable salt, hydrate, solvate, or N-oxide thereof.

Assignments (2)
SECURITY INTEREST Recorded Aug 25, 2022
From: RIGEL PHARMACEUTICALS, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 061327/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2004
From: SINGH, RAJINDER; GOFF, DANE; PARTRIDGE, JOHN J.
To: RIGEL PHARMACEUTICALS, INC.
Reel/Frame 015677/0533 →