IP Library Granted Patent US 7,728,141
Granted Patent B2
US 7,728,141 · App. 10/576,796 · Granted Jun 1, 2010

Substituted naphthyridinone derivatives

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Quick Facts
Patent No.
US 7,728,141
App. No.
10/576,796
Granted
Jun 1, 2010
Kind
B2
Abstract

Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, and cirrhosis of the liver.

Claims (225)

1. A compound of structural formula I:

and pharmaceutically acceptable salts thereof, wherein:

R 1 is selected from:

(1) hydrogen,

(2) halogen,

(3) C 1-4 alkyl,

(4) —CN,

(5) —C(O)R 7 ,

(6) —OR d ,

(7) —NR 5 R 6 , and

(8) pyrrolidinyl,

wherein: alkyl moieties are unsubstituted or substituted with one substituent independently selected from R a ;

R 2 is selected from: —NR 5 R 6 , and C 1-6 alkyl;

R 3 is hydrogen;

R 4 is selected from:

(1) hydrogen, and

(2) —CH 2 —R 8 ;

R 5 is selected from:

(1) hydrogen,

(2) C 1-6 alkyl,

(3) trifluoromethyl, and

(4) methylcarbonyl,

R 6 is each selected from:

(1) hydrogen,

(2) C 1-6 alkyl,

(3) phenyl,

(4) benzyl,

(5) trifluoromethyl,

(6) —C(O)—R c ,

(7) —CO 2 R c , and

(8) —S(O) 2 CH 3 ,

or R 5 and R 6 together form ═CH—N(CH 3 ) 2 ;

R 7 is selected from:

(1) hydrogen,

(2) C 1-3 alkyl,

(3) —OR e , and

(4) —NR d R e ,

wherein the alkyl moieties are unsubstituted or substituted with one, two, or three substituents independently selected from R a ;

R 8 is selected from:

(1) hydrogen,

(2) —(CH 2 ) n OC(O)CH 3 ,

(3) C 1-6 alkyl,

(4) C 3-6 cycloalkyl,

(5) tetrahydrofuranyl,

(6) phenyl, and

(7) pyridyl;

wherein the alkyl moieties are unsubstituted or substituted with one substituent independently selected from —OR e , and the tetrahydrofuranyl, phenyl, and pyridyl moieties are unsubstituted or substituted with one, or two substituents independently selected from OR e , halogen, —NR e R f , —COCH 3 , —C(O)OCH 3 , —CN, and C 1-3 alkyl;

Ar 1 and Ar 2 are each phenyl, unsubstituted or substituted with one or two substituents independently selected from R b ;

each R a is independently selected from: —OR e , halogen, —NR e R f , —C(O)R c , —CO 2 R c , —OC(O)R c , —CN, CF 3 , and —OCF 3 ;

each R b is independently selected from:

(1) R a , and

(2) C 1-10 alkyl;

each R c is independently selected from: hydrogen, C 1-6 alkyl, and —NR d R d ; wherein each alkyl moiety may be substituted with one or two substituents selected from R h and oxo;

each R d is independently selected from hydrogen, and C 1-6 alkyl;

R e and R f are is independently selected from hydrogen and C 1-3 alkyl;

each R h is independently selected from:

(1) halogen,

(2) C 1-10 alkyl,

(3) —OR i ,

(4) —NR i R i , and

(5) —OC(O)R i ,

each R i is independently selected from:

(1) hydrogen,

(2) C 1-3 alkyl,

(3) trifluoromethyl, and

(4) cyclopropyl;

wherein each alkyl and cycloalkyl moiety is unsubstituted or substituted with one substituent selected from oxo, hydroxy, methoxy, acetoxy, halogen, cyano, and trifluoromethyl;

and

n is 1;

or a pharmaceutically acceptable salt thereof.

2. The compound according to claim 1 , wherein;

each R a is independently selected from: hydroxy, methoxy-, halogen, methylcarbonyl-, —CO 2 R c , —OC(O)R c , —CN, CF 3 , and —OCF 3 ;

each R d is independently selected from hydrogen, methyl, and ethyl;

each R h is independently selected from:

(1) halogen;

(2) C 1-3 alkyl;

(3) hydroxy;

(4) methoxy-; and

(5) —NR i R i ,

wherein R i is selected from hydrogen and methyl; methylcarbonyloxy- ; —CF 3 ; and —OCF 3 ;

or a pharmaceutically acceptable salt thereof.

3. The compound according to claim 2 , wherein

R 1 is selected from:

(1) halogen;

(2) C 1-3 alkyl, unsubstituted or substituted with hydroxy or methoxy;

(3) —CN;

(4) methyloxycarbonyl-;

(5) methylcarbonyl-;

(6) isopropyloxycarbonyl-;

(7) bromomethylcarbonyl-;

(8) —C(O)NH 2 ;

(9) methoxy-; and

(10) —NR 5 R 6 , wherein R 5 is methyl and R 6 is C 1-3 alkyl;

each R i is independently selected from: hydrogen, and methyl;

and pharmaceutically acceptable salts thereof.

4. The compound according to claim 2 , wherein

R 5 is selected from: hydrogen, methyl, and methlcarbonyl-, and

R 6 is hydrogen, C 1-3 alkyl, methyl benzyl, —C(═O)R c , or —SO 2 CH 3 ;

R 7 is selected from:

(1) C 1-3 alkyl, unsubstituted or substituted with halogen;

(2) —OR e ; and

(3) —NR d R e ;

wherein R d is selected from hydrogen and methyl, and R e is selected from hydrogen and C 1-3 alkyl;

and pharmaceutically acceptable salts thereof.

5. The compound according to claim 4 , wherein:

R 1 is selected from:

(1) —C(O)CH 3 ,

(2) —CH(OH)CH 3 ,

(3) —CH 3 ,

(4) —CH 2 CH 3 ,

(5) —CH(CH 3 ) 2 ,

(6) —CH(OCH 3 )(CH 3 ),

(7) —C(O)—OCH 3 ,

(8) —C(O)OCH(CH 3 ) 2 ,

(9) —CN, —C(O)NH 2 ,

(10) —C(O)N(CH 3 ) 2 ,—

(11) Cl

(12) —N(CH 3 ) 2 ,

(13) —N(CH 3 )(CH(CH 3 ) 2 ), and

(14) pyrrolidinyl;

R 2 is or C 1-6 alkyl or NR 5 R 6 , wherein R 5 is selected from: hydrogen, methyl, and methylcarbonyl-, and R 6 is selected from, hydrogen, methyl benzyl, —C(═O)R c , and —SO 2 CH 3 ;

R 5 is selected from: hydrogen, methyl, and methlcarbonyl-, and

R 6 is hydrogen, C 1-3 alkyl, methyl benzyl, or —C(═O)R c ;

Ar 1 is phenyl, substituted with one or two substituents independently selected from halogen and methyl;

Ar 2 is phenyl, either unsubstituted or substituted with one or two halogen substituents;

or a pharmaceutically acceptable salt thereof.

6. The compound according to claim 1 , of structural formula IA:

wherein R 1 , R 2 , and R 4 are as defined in claim 1 ;

and pharmaceutically acceptable salts thereof.

7. A compound selected from:

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

3-acetyl-4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-1,8-naphthyridin-2(1H)-one;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-(1-hydroxyethyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-1,8-naphthyridin-2(1H)-one;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-ethyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

3-acetyl-4-(benzylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-1,8-naphthyridin-2(1H)-one;

3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-4-(dimethylamino)-1-methyl-1,8-naphthyridin-2(1H)-one;

N′-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N,N-dimethylurea;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N-methylacetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-2-methoxyacetamide;

N-[3-acetyl-1-benzyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-6-(4-chlorophenyl)-1-(cyclopropylmethyl)-7-(2,4-dichlorophenyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-1-butyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-(2-methoxyethyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1-(tetrahydrofuran-2-ylmethyl)-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

2-{[3-acetyl-4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1,8-naphthyridin-1(2H)-yl]methyl}pyridinium trifluoroacetate;

3-{[3-acetyl-4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1,8-naphthyridin-1(2H)-yl]methyl}pyridinium trifluoroacetate;

2-[3-acetyl-4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1,8-naphthyridin-1(2H)-yl]ethyl acetate;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-(2,4-dimethoxybenzyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

4-{[3-acetyl-4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1,8-naphthyridin-1(2H)-yl]methyl}pyridinium trifluoroacetate;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1-propyl-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-7-(2-chlorophenyl)-6-(4-chlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-(1-(2,4-dimethoxybenzyl)-3-acetyl-7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-2-oxo-1,8-naphthyridin-4-yl)-N-acetylacetamide;

N-(1-(2,4-dimethoxybenzyl)-7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-2-oxo-1,8-naphthyridin-4-yl)-N-acetylacetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-(2-hydroxyethyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]methanesulfonamide;

2-{[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]amino}-2-oxoethyl acetate;

N-[3-acetyl-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-2-hydroxyacetamide;

N-[3-acetyl-7-(2,4-dichlorophenyl)-1-methyl-6-(4-methylphenyl)-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-acetyl-7-(4-chlorophenyl)-6-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1,3-dimethyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]propanamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-ethyl-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]butanamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1,3-dimethyl-1,8-naphthyridin-2(1H)-one;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1,3-dimethyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-1,8-naphthyridin-2(1H)-one;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N-methylacetamide;

2-{[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]amino}-2-oxoethyl acetate;

2-chloro-N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-2-methoxyacetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N′-ethylurea;

N-[3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-2-hydroxyacetamide;

N 1 -[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N 2 ,N 2 -dimethylglycinamide;

N 1 -[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N 2 -methylglycinamide;

N 1 -[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]glycinamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-ethyl-1-methyl-1,8-naphthyridin-2(1H)-one;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-isopropyl-1-methyl-1,8-naphthyridin-2(1H)-one;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-methyl-1-propyl-1,8-naphthyridin-2(1H)-one;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-ethyl-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-isopropyl-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-methyl-2-oxo-1-propyl-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-ethyl-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-(1-methoxyethyl)-1-methyl-1,8-naphthyridin-2(1H)-one;

4-amino-3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-1,8-naphthyridin-2(1H)-one;

N-[3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

4-amino-3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-1,8-naphthyridin-2(1H)-one;

N-acetyl-N-(3-chloro-7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-1-isobutyl-2-oxo-1,8-naphthyridin-4-yl)acetamide;

N-[3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N 1 -[3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N 2 ,N 2 -dimethylglycinamide;

2-{[3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]amino}-2-oxoethyl acetate;

N-[3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-2-hydroxyacetamide;

N-acetyl-N-(3-chloro-7-(2-chlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-1-isobutyl-2-oxo-1,8-naphthyridin-4-yl)acetamide;

N-[3-chloro-7-(2-chlorophenyl)-6-(4-chlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[3-chloro-7-(2-chloro-4-fluorophenyl)-6-(4-chlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-(dimethylamino)-1-methyl-1,8-naphthyridin-2(1H)-one;

N-acetyl-N-(7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-3-(dimethylamino)-1,2-dihydro-1-methyl-2-oxo-1,8-naphthyridin-4-yl)acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-(dimethylamino)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-[isopropyl(methyl)amino]-1-methyl-1,8-naphthyridin-2(1H)-one;

N-(3-(N-isopropyl-N-methylamino)-7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-1-methyl-2-oxo-1,8-naphthyridin-4-yl)-N-acetylacetamide;

N-{6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-[isopropyl(methyl)amino]-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl}acetamide;

N-acetyl-N-(7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-1-methyl-2-oxo-3-(pyrrolidin-1-yl)-1,8-naphthyridin-4-yl)acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-3-pyrrolidin-1-yl-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-methoxy-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N-acetyl-N-(7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-1-isobutyl-3-methoxy-2-oxo-1,8-naphthyridin-4-yl)acetamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methoxy-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

N′-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N,N-dimethylimidoformamide;

N′-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-ethyl-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N,N-dimethylimidoformamide;

N′-[3-chloro-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N,N-dimethylimidoformamide;

N′-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-isobutyl-3-methoxy-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]-N,N-dimethylimidoformamide;

N-[6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-(1-methoxyethyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-3-isopropyl-1-methyl-4-(methylamino)-1,8-naphthyridin-2(1H)-one;

methyl 4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate;

methyl 4-(N-acetylacetamido)-7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-1,2-dihydro-1-methyl-2-oxo-1,8-naphthyridine-3-carboxylate;

isopropyl 4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate;

ethyl 4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamide;

4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-N,N,1-trimethyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamide;

4-amino-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carbonitrile;

N-[6-(4-chlorophenyl)-3-cyano-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-4-yl]acetamide;

and pharmaceutically acceptable salts thereof.

8. A composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier.

Assignments (2)
CHANGE OF NAME Recorded Jan 22, 2010
From: MERCK & CO., INC.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 023834/0029 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2006
From: DEBENHAM, JOHN S.; DOSS, GEORGE A.; MADSEN-DUGGAN, CHRISTINA B.; WALSH, THOMAS F.
To: MERCK & CO., INC.
Reel/Frame 017641/0819 →