IP Library Granted Patent US 7,893,066
Granted Patent B2
US 7,893,066 · App. 12/082,332 · Granted Feb 22, 2011

Pyridol[2,3-B]pyrazinones for use as stearoyl CoA desaturase inhibitors

Assignee: Gilead Palo Alto, Inc.
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Quick Facts
Patent No.
US 7,893,066
App. No.
12/082,332
Granted
Feb 22, 2011
Kind
B2
Abstract

The present invention discloses pyrido[2,3-B]pyrazinones having the structure of Formula I for use as inhibitors of stearoyl-CoA desaturase. The compounds are useful in treating and/or preventing various human diseases, mediated by stearoyl-CoA desaturase (SCD) enzymes, especially diseases related to abnormal lipid levels, cardiovascular disease, diabetes, obesity, oily skin conditions, metabolic syndrome, and the like.

Claims (147)

1. A compound having the structure of Formula I:

wherein

R 1 is

a) optionally substituted 4 to 6 membered nitrogen containing monocyclic heterocycle,

b) —X—NR 4 R 5 ,

c) —X—C(O)NR 4 R 5 ,

d) —X—C(O)OR 7 ,

e) —X—OR 7 , or

f) —X—NR 8 —C(O)NR 4 R 5

wherein

R 4 is hydrogen or C 1-4 alkyl, and

R 5 is hydrogen, C 1-4 alkyl, aryl, heteroaryl, C 1-4 alkoxy, —C(═NH)NH 2 ,—C(═O)R 6 or —S(═O) 2 R 6 , wherein

R 6 is hydrogen, optionally substituted C 1-4 alkyl, C 1-4 alkenyl, C 1-4 alkoxy, optionally substituted monocyclic aryl, or 5 or 6 membered optionally substituted monocyclic heteroaryl, or

R 4 and R 5 along with the nitrogen to which they are attached join to form a 5 or 6 membered monocyclic heteroaryl or heterocyclyl ring;

R 7 is hydrogen, optionally substituted C 1-4 alkyl, C 1-4 alkenyl, optionally substituted monocyclic aryl, or 5 or 6 membered optionally substituted monocyclic heteroaryl;

R 8 is hydrogen or C 1-4 alkyl;

X is optionally substituted C 1-4 linear or branched alkylene;

R 2 is optionally substituted mono or bicyclic aryl or mono or bicyclic heteroaryl;

wherein the aryl or heteroaryl moiety is optionally substituted with from 1 to 3 substituents independently selected from the group consisting of alkyl, heterocyelyl, aryl, heteroaryl, halo, NO 2 , CF 3 , CN, OR 20 , SR 20 , N(R 20 ) 2 , S(O)R 22 , SO 2 R 22 , SO 2 N(R 20 ) 2 , S(O) 3 R 20 ,P(O)(OR 20 ) 2 , SO 2 NR 20 COR 22 , SO 2 NR 20 CO 2 R 22 , SO 2 NR 20 CON(R 20 ) 2 , NR 20 COR 22 R 22 , NR 20 CO 2 R 22 , NR 20 CON(R 20 ) 2 , NR 20 C(NR 20 )NHR 23 , COR 20 , CO 2 R 20 , CON(R 20 ) 2 , CONR 20 SO 2 R 22 , NR 20 SO 2 R 22 , SO 2 NR 20 CO 2 R 22 , OCONR 20 SO 2 R 22 , OC(O)R 20 , C(O)OCH 2 OC(O)R 20 , and OCON(R 20 ) 2 , and

further wherein each optional alkyl, heteroaryl, aryl, and heterocyclyl substituent is further optionally substituted with halo, NO 2 , alkyl, CF 3 , amino, mono- or di-alkylamino, alkyl or aryl or heteroaryl amide, NR 20 COR 22 , NR 20 SO 2 R 22 , COR 20 , CO 2 R 20 , CON(R 20 ) 2 , NR 20 CON(R 20 ) 2 , OC(O)R 20 , OC(O)N(R 20 ) 2 , S(O) 3 R 20 , P(O)(OR 20 ) 2 , SR 20 , S(O)R 22 , SO 2 R 22 , SO 2 N(R 20 ) 2 , CN, or OR 20 ;

R 3 is hydrogen, optionally substituted C 1-4 alkyl, optionally substituted monoeyclic aryl or 5 or 6 membered optionally substituted monocyclic heteroaryl;

wherein the alkyl, cycloalkyl, aryl, heterocyclyl or heteroaryl moiety is optionally substituted with from 1 to 3 substituents independently selected from the group consisting of alkyl, heterocyclyl, aryl, heteroaryl, halo, NO 2 , CF 3 , CN, OR 20 , SR 20 , N(R 20 ) 2 , S(O)R 22 , SO 2 R 22 , SO 2 N(R 20 ) 2 , S(O) 3 R 20 , P(O)(OR 20 ) 2 , SO 2 NR 20 COR 22 , SO 2 NR 20 CO 2 R 22 , SO 2 NR 20 CON(R 20 ) 2 , NR 20 COR 22 , NR 20 CO 2 R 22 , NR 20 CON(R 20 ) 2 , NR 20 C(NR 20 )NHR 23 , COR 20 , CO 2 R 20 , CON(R 20 ) 2 , CONR 20 SO 2 R 22 , NR 20 SO 2 R 22 , SO 2 NR 20 CO 2 R 22 , OCONR 20 SO 2 R 22 , OC(O)R 20 , C(O)OCH 2 OC(O)R 20 , and OCON(R 20 ) 2 , and

further wherein each optional alkyl, heteroaryl, aryl, and heterocyclyl substituent is further optionally substituted with halo, NO 2 , alkyl, CF 3 , amino, mono- or di-alkylamino, alkyl or aryl or heteroaryl amide, NR 20 COR 22 , NR 20 SO 2 R 22 , COR 20 , CO 2 R 20 , CON(R 20 ) 2 , NR 20 CON(R 20 ) 2 , OC(O)R 20 ,) OC(O)N(R 20 ) 2 , S(O) 3 R 20 , P(O)(OR 20 ) 2 , SR 20 , S(O)R 22 , SO 2 R 22 , SO 2 N(R 20 ) 2 , CN, or OR 20 ;

R 20 and R 22 are independently selected from the group consisting of hydrogen, C 1-15 alkyl, C 2-15 alkenyl, C 2- 15 alkynyl, heteroeyclyl, aryl, and heteroaryl,

wherein the alkyl, alkenyl, alkynyl, heterocyclyl, aryl, and heteroaryl moieties are optionally substituted with from 1 to 3 substituents independently selected from halo, alkyl, mono- or dialkylamino, alkyl or aryl or heteroaryl amide, CN, O—C 1-6 alkyl, CF 3 , aryl, and heteroaryl;

Q is C 1-4 alkylene which may optionally contain one or more —NH—, —O—, —S—, or carbonyl linking moieties;

wherein the R 2 -Q-NH— moiety is attached to the ‘a’ or ‘b’ position indicated in Formula I, provided that W 1 is C when the R 2 -Q-NH— moiety is attached to the ‘a’ position;

or a pharmaceutically acceptable salt or ester thereof.

2. The compound of claim 1 , wherein R 1 is —X—NR 4 R 5 , —X—C(O)NR 4 R 5 , —X—C(O)OR 7 , or —X—OR 7 and R 2 is optionally substituted 5 or 6 membered monocyclic aryl or 5 or 6 membered monocyclic heteroaryl.

3. The compound of claim 1 , wherein R 1 is —X—NR 4 R 5 and R 3 is optionally substituted monocyclic aryl.

4. The compound of claim 3 , selected from the group consisting of:

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(6-{[(4-fluorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(6-{[(3-chlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(6-{[(3-chloro-4-fluorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-{2-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[2-(4-methoxyphenyl)-3-oxo-6-({[4-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methylthiophenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methylphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(6-{[(3-bromophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-{2-[6-({[3,5-bis(trifluoromethyl)phenyl]methyl}amino)-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[6-({[4-fluoro-3-(trifluoromethyl)phenyl]methyl}amino)-2-(4-methoxyphenyl) -3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[2-(4-methoxyphenyl)-3-oxo-6-({[5-(trifluoromethyl)(3-pyridyl)]methyl}amino) -4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-(2-{2-(4-methoxyphenyl)-3-oxo-6-[benzylamino]-4-hydropyridino[2,3-b]pyrazin-4-yl}ethyl)acetamide;

N-(2-{2-(4-methoxyphenyl)-3-oxo-6-[(3-pyridylmethyl)amino]-4-hydropyridino[2,3-b]pyrazin-4-yl}ethyl)acetamide;

N-[2-(6-{[(3-fluorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin -4-yl)ethyl]acetamide;

4-(2-aminoethyl)-6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-4-hydropyridino[3,2-b]pyrazin-3-one;

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))ethyl](tert-butoxy)carboxamide;

N-[2-(6-{[(2-chlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-(2-{2-(4-methoxyphenyl)-3-oxo-6-[(3-phenylpropyl)amino]-4-hydropyridino[2,3-b]pyrazin-4-yl}ethyl)acetamide;

N-{2-[2-(4-methoxyphenyl)-3-oxo-6-({[6-(trifluoromethyl)(2-pyridyl)]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-[2-(2-(4-methoxyphenyl)-6-{[(5-methyl(1,2,4-oxadiazol-3-yl))methyl]amino}-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(2-(4-methoxyphenyl)-6-{[(3-methoxyphenyl)methyl]amino}-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

methyl 3-[({4-[2-(acetylamino)ethyl]-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[5,6-b]pyrazin-6-yl}amino)methyl]benzoate;

3-[({4-[2-(acetylamino)ethyl]-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[5,6-b]pyrazin-6-yl}amino)methyl]benzoic acid;

N-[2-(2-(4-methoxyphenyl)-6-{[(3-methylphenyl)methyl]amino}-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-{2-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethoxy)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-(2-{2-(4-methoxyphenyl)-3-oxo-6-[(2-pyridylmethyl)amino]-4-hydropyridino[2,3-b]pyrazin-4-yl}ethyl)acetamide;

N-{2-[6-({[2-fluoro-5-(trifluoromethyl)phenyl]methyl}amino)-2-(4-methoxyphenyl) -3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-[2-(2-(4-methoxyphenyl)-6-{[(5-methylisoxazol-3-yl)methyl]amino}-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-{2-[2-[4-(2-methoxyethoxy)phenyl]-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[3-oxo-2-(4-propylphenyl)-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[2-[4-(acetylamino)phenyl]-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[2-(4-methylphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[2-(4-ethylphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[2-(4-fluorophenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))ethyl]-2-(dimethylamino)acetamide;

{N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]carbamoyl}methyl acetate;

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))ethyl]-2-hydroxyacetamide;

2-amino-N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))ethyl]acetamide

2-(acetylamino)-N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl) -3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))ethyl]acetamide;

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-[4-(methylsulfonyl)phenyl]-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(2-(3,4-dichlorophenyl)-6-{[(3,4-dichlorophenyl)methyl]amino}-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(6- { [3-(2,5-dichlorophenoxy)propyl]amino }-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino [2,3-b]pyrazin-4-yl)ethyl]acetamide;

{N-[2-(4-methoxyphenyl)-3-oxo-6-({ [3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]carbamoyl}methyl acetate;

N- {2-[3-oxo-2[4-(trifluoromethyl)phenyl]-6-({[3-(trifluoromethyl)Phenyl]methyl}amino)-4-hydropyridino [2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-(2-(7-(3,4-dichlorobenzylamino)-2-(4-methoxyphenyl)-3-oxopyrido[2,3-]pyrazin-4(3H)-yl)ethyl)acetamide;

N-(2-(2-(4-methoxyphenyl)-3-oxo-7-(3-(trifluoromethyl)benzylamino)pyrido [2,3-b]pyrazin-4(3H)-yl)ethyl)acetamide;

N-(2-(7-(4-chlorobenzylamino)-2-(4-methoxyphenyl)-3-oxopyrido[2,3-b]pyrazin -4(3H)-yl)ethyl)acetamide;

N-(2-(7-(3-chlorobenzylamino)-2-(4-methoxyphenyl)-3-oxopyrido[2,3-b]pyrazin -4(3H)-yl)ethyl)acetamide;

N-(2-(7-(4-methoxybenzylamino)-2-(4-methoxyphenyl)-3-oxopyrido[2,3-b]pyrazin -4(3H)-yl)ethyl)acetamide;

N-(2-(7-(3,4-dichlorophenethylamino)-2-(4-methoxyphenyl)-3-oxopyrido[2,3-b]pyrazin -4(3H)-yl)ethyl)acetamide; and

N-(2-(7-(3,4-dichlorobenzylamino)-2-(3,4-dichlorophenyl)-3-oxopyrido[2,3-b]pyrazin -4(3H)-yl)ethypacetamide.

5. The compound of claim 2 , wherein R 1 is —X—NR 4 R 5 and R 3 is 5 or 6 membered optionally substituted monocyclic heteroaryl.

6. The compound of claim 5 , selected from the group consisting of:

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-3-oxo-2-(3-pyridyl)-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-[2-(6-{[(3-chloro-4-fluorophenyl)methyl]amino}-3-oxo-2-(3-pyridyl)-4-hydropyridino[2,3-b]pyrazin-4-yl)ethyl]acetamide;

N-{2-[3-oxo-2-(3-pyridyl)-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide; and

N-(2-(7-(3,4-dichlorobenzylamino)-3-oxo-2-(pyridin-3-yl)pyrido[2,3-b]pyrazin -4(3H)-yl)ethyl)acetamide.

7. The compound of claim 2 , wherein R 1 is —X—NR 4 R 5 and R 3 is hydrogen.

8. The compound of claim 7 , selected from the group consisting of:

N-{2-[3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide; and

N-[2-(6-{[(3,4-dichlorophenyl)methyl]amino}-3-oxo-4-hydropyridino[2,3-b]pyrazin -4-yl)ethyl]acetamide.

9. The compound of claim 2 , wherein R 3 is optionally substituted C 1-4 alkyl.

10. The compound of claim 9 , selected from the group consisting of:

N-{2[3-oxo-2-(trifluoromethyl)-6-({ [3-(trifluoromethyl)phenyl]methyl}amino -4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl acetamide;

N-{2-[2-methyl-3-oxo-6-({[3 (trifluoromethyl )phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

N[2-(6- {[(3,4-dichlorophenyl)methyl]amino}-2-methyl-3-oxo-4-hydropyridino [2,3 -b]pyrazin-4-yl)ethyl]acetamide;

ethyl 4-[2-(acetylamino)ethyl]-3-oxo-6-({[3 -(trifluoromethyl)phenyl]methyl amino) -4-hydropyridino [2,3-e]pyrazine-2-carboxylate;

4-[2-(acetylamino)ethyl]3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino [2,3-b]pyrazine-2-carboxylic acid;

N- {2-[3-oxo-2-propyl-6-({[3-(trifluoromethyl)phenyl]methyl amino)-4-hydropyridino [2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2-[2-ethyl-3-oxo-6-(}[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino [2,3-b]pyrazin-4-yl]ethyl}acetamide;

N-{2[3-oxo-2-(2-phenylethyl)-6-(}[3-trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]ethyl}acetamide;

4-[2-methyl-3-oxo-6-({[3-(trifluoromethyl)pheny[methyl}amino)-4-hydropyridino [2,3-b]pyrazin-4-yl]butanamide;

N-(2-(7-(benzylamino)-2-methyl-3-oxopyrido [2,3-b]pyrazin-4(3H) -yl)ethyl)acetamide; and

benzyl 4-(2-acetamidoethyl)-2-methyl-3-oxo- 1,2,3,4-tetrahydropyri do [2,3-b]pyrazin -7-ylcarbarmate.

11. The compound of claim 2 , wherein R 1 is —X—C(O)NR 4 R 5 and R 3 is optionally substitutedmonocyclic aryl.

12. The compound of claim 11 , selected from the group consisting of:

3-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)propanamide;

3-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanamide;

4-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))-N-methylbutanamide;

4-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4- hydropyridino[2,3-b]pyrazin-4-yl)butanamide; and

3-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))-N-methylpropanamide;

3-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)(4-hydropyridino[2,3-b]pyrazin-4-yl)]-N-(phenylmethoxy)propanamide;

N-methoxy-3-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)(4-hydropyridino[2,3-b]pyrazin-4-yl)]propanamide;

3-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)(4-hydropyridino[2,3-b]pyrazin-4-yl)]-N-methylpropanamide;

3-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanehydroxamic acid;

(3R)-3-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)(4-hydropyridino[2,3-b]pyrazin-4-yl)]butanamide;

3-[2-(4-methylphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanamide;

3-[2-(4-ethylphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanamide;

3-[2-[4-(2-methoxyethoxy)phenyl]-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanamide;

3-[3-oxo-2-(4-propylphenyl)-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanamide;

4-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]butanamide;

3-[3-oxo-2-[4-(trifluoromethyl)phenyl]-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanamide;

2-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]acetamide;

(3S)-3-[2-(4-methoxyphenyl)-3-oxo-6-({[3-(trifluoromethyl)phenyl]methyl}amino)(4-hydropyridino[2,3-b]pyrazin-4-yl)]butanamide; and

3-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))-N-(2-hydroxyethyl)propanamide.

13. The compound of claim 2 , wherein R 1 is —X—C(O)NR 4 R 5 and R 3 is 5 or 6 membered optionally substituted monocyclic heteroaryl.

14. The compound of claim 13 , selected from the group consisting of:

3-(6-{[(3,4-dichlorophenyl)methyl]amino}-3-oxo-2-(3-pyridyl)-4-hydropyridino[2,3-b]pyrazin-4-yl)propanamide; and

3-[3-oxo-2-(3-pyridyl)-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[2,3-b]pyrazin-4-yl]propanamide.

15. The compound of claim 2 , wherein R 1 is —X—C(O)OR 7 and R 3 is optionally substituted monocyclic aryl.

16. The compound of claim 15 , selected from the group consisting of:

ethyl 3-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)propanoate;

ethyl 4-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)butanoate;

4-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)butanoic acid; and

3-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo-4-hydropyridino[2,3-b]pyrazin-4-yl)propanoic acid.

17. The compound of claim 2 , wherein R 1 is —X—OR 7 .

18. The compound of claim 17 , wherein X is ethylene, R 2 is 3-(trifluoromethyl), R 3 is 4-methoxyphenyl, and R 5 is hydrogen, namely 4-(2-hydroxyethyl)-2-(4-methoxyphenyl)-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[3,2-b]pyrazin -3-one.

19. The compound of claim 2 , wherein R 1 is —X—NR 8 —C(O)NR 4 R 5 .

20. The compound of claim 1 wherein R 1 is a 4 to 6 membered nitrogen containingmonocyclic heterocycle.

21. The compound of claim 20 , selected from the group consisting of:

4-((3R)pyrrolidin-3-yl)-6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-4-methoxyphenyl)-4-hydropyridino[3,2-b]pyrazin-3-one;

(3R)-3-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))pyrrolidinecarbaldehyde;

(3S)-3-(6-{[(3,4-dichlorophenyl)methyl]amino}-2-(4-methoxyphenyl)-3-oxo(4-hydropyridino[2,3-b]pyrazin-4-yl))pyrrolidinecarbaldehyde; and

4-((3S)-6-oxo(3-piperidyl))-2-(4-methoxyphenyl)-6-({[3-(trifluoromethyl)phenyl]methyl}amino)-4-hydropyridino[3,2-b]pyrazin-3-one.

22. A pharmaceutical composition comprising a therapeutically effective amount of thecompound of claim 1 or a pharmaceutically acceptable salt, ester, prodrug, or hydrate thereof.

Assignments (2)
MERGER Recorded Jun 28, 2010
From: CV THERAPEUTICS, INC.
To: GILEAD PALO ALTO, INC.
Reel/Frame 024601/0306 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2009
From: KOLTUN, DMITRY; ZABLOCKI, JEFF; PARKHILL, ERIC; GLUSHKOV, ANDREI; VASILEVICH, NATALYA; IVANOV, ALEXEY; ZILBERSHTEIN, TIMUR; CHISHOLM, JEFFREY
To: CV THERAPEUTICS, INC.
Reel/Frame 022658/0400 →
Continuity (3)
Continuation In Part 11868386 · Oct 5, 2007
Provisional Application 60849648 · Oct 5, 2006
Related Publication 20080255130A1 · Oct 16, 2008