IP Library › Granted Patent US 8,735,584
Granted Patent B2
US 8,735,584 · App. 12/919,136 · Granted May 27, 2014

Protein kinase inhibitors and use thereof

Inventors: Bayard R. Huck (Sudbury, MA); Xiaoling Chen (Chestnut Hill, MA); Lizbeth Celeste Deselm (Melrose, MA); Christopher Charles Victor Jones (Arlington, MA); Srinivasa R. Karra (Pembroke, MA); Yufang Xiao (Lexington, MA); Andreas Goutopoulos (Boston, MA); Amanda E. Sutton (Hingham, MA)
Assignee: Merck Patent GmbH
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Quick Facts
Patent No.
US 8,735,584
App. No.
12/919,136
Granted
May 27, 2014
Kind
B2
Abstract

Disclosed are benzonaphthyridinyl derivative compounds and analogs thereof, pharmaceutical compositions comprising such compounds and processes for preparing the same. The compounds are useful in the treatment of diseases amenable to kinase signal transduction inhibition, regulation or modulation.

Claims (64)

1. A compound according to formula V:

which conforms to subformulae; A, B, C, D, E, F, G, H, J, K, L and M of formula (V), wherein:

in Subformula A

R 9 is phenyl, unsubstituted, or monosubstituted or independently disubstituted, by methoxy, CF 3 , F, CH 3 or Cl,

R 8 is H or F,

one of R 4 , R 5 , R 6 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4- Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N-(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3-(dimethylamino)propyl)carbamoyl or CF 3 , while the remaining two of R 4 , R 5 , R 6 are H,

in Subformula B

R 9 is phenyl, unsubstituted, or monosubstituted, or independently disubstituted, by methoxy, CF 3 , F, CH 3 or Cl,

R 8 is H,

one of R 4 , R 5 , R 6 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N-(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3-(dimethylamino)propyl) carbamoyl or CF 3 , while the remaining two of R 4 , R 5 , R 6 are H,

in Subformula C

R 9 is phenyl, unsubstituted, or monosubstituted, or independently disubstituted, by methoxy, CF 3 , F, CH 3 or Cl,

R 8 is H,

R 4 , R 5 , R 6 are H,

in Subformula D

R 9 is phenyl,

R 8 is H,

one of R 4 , R 5 , R 6 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4- Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N-(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, carboxylic acid 2-morpholin-4-yl-ethyl amidyl, N-(3-(dimethylamino)propyl)carbamoyl or CF 3 , while the remaining two of R 4 , R 5 , R 6 are H,

in Subformula E

R 9 is phenyl, unsubstituted, or monosubstituted, or independently disubstituted, by methoxy, CF 3 , F, CH 3 or Cl,

R 8 is H,

R 4 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N -(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl -propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3- (dimethylamino)propyl)carbamoyl or CF 3 , R 5 , R 6 are H,

in Subformula F

R 9 is phenyl, unsubstituted, or monosubstituted, or independently disubstituted, by methoxy, CF 3 , F, CH 3 or Cl,

R 8 is H,

R 5 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N -(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3- (dimethylamino)propyl)carbamoyl or CF 3 ,

R 4 , R 6 are H,

in Subformula G

R 9 is phenyl, unsubstituted, or monosubstituted, or independently disubstituted, by methoxy, CF 3 , F, CH 3 or Cl,

R 8 is H,

R 6 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N -(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3- (dimethylamino)propyl)carbamoyl or CF 3 , R 4 , R 5 are H,

in Subformula H

R 9 is phenyl, substituted by CF 3 and F,

R 8 is H,

one of R 4 , R 5 , R 6 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N-(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3-(dimethylamino)propyl)carbamoyl or CF 3 , while the remaining two of R 4 , R 5 , R 6 are H,

in Subformula J

R 9 is phenyl, substituted by CF 3 and F,

R 8 is H,

R 6 is hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N-(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3- (dimethylamino)propyl)carbamoyl or CF 3 , R 4 , R 5 are H,

in Subformula K

R 9 is phenyl,

R 8 is H,

R 5 , R 6 are independently hydroxymethyl, N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine-1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N-(2,3-dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3-(dimethylamino)propyl)carbamoyl or CF 3 , R 4 is H,

in Subformula L

R 9 is cyclohexyl, phenylamino, (trifluoromethyl)pyridyl,

R 8 is H, one of R 4 , R 5 , R 6 is hydroxymethyl,

N-(2-(dimethylamino)ethyl)carbamoyl, COONH2, (4-Methylpiperazine- 1-carbonyl), COOCH 3 , COOH, N-(2-aminoethyl)carbamoyl, N-(2,3 -dihydroxypropyl)carbamoyl, COOCH 2 CH 3 , aminomethyl, 3-morpholin-4-yl-propyl amidyl, 2-hydroxy ethyl amidyl, methoxy, F, Cl, 2-morpholin-4-yl-ethyl amidyl, N-(3-(dimethylamino)propyl)carbamoyl or CF 3 , while the remaining two of R 4 , R 5 , R 6 are H and

in Subformula M

R 9 is phenyl, unsubstituted, or monosubstituted, or independently disubstituted, by methoxy, CF 3 , F, CH 3 or Cl,

R 8 is H,

R 4 , R 5 are methoxy,

R 6 is H.

2. A compound selected from the group consisting of:

Methyl 1-(4-benzamidophenylamino)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxylate;

N-(4-(9-(Hydroxymethyl)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridin-1-ylamino)phenyl)benzamide;

1-(4-Benzamidophenylamino)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxylic acid;

1-(4-benzamidophenylamino)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamide;

1-(4-Benzamidophenylamino)-N,N-dimethyl-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamide;

N-(2-Aminoethyl)-1-(4-benzamidophenylamino)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamide;

1-(4-benzamidophenylamino)-N-(2-(dimethylamino)ethyl)-6-oxo-5,6-dihydrobenzo[c] [1,8]naphthyridine-9-carboxamide;

1-(4-benzamidophenylamino)-N-(2-(4-methylpiperazin-1-yl)ethyl)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamide;

1-(4-Benzamidophenylamino)-N-(2-hydroxyethyl)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamide;

N-(4-(9-Chloro-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridin-l-ylamino)phenyl)benzamide; and

1-(4-(3,4-Difluorobenzamido)phenylamino)-N-(2-(dimethylamino)ethyl)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-9-carboxamide.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2010
From: HUCK, BAYARD; CHEN, XIAOLING; DESELM, LIZBETH C.; JONES, CHRISTOPHER C.V.; KARRA, SRINIVASA; XIAO, YUFANG; GOUTOPOULOS, ANDREAS; SUTTON, AMANDA E.
To: MERCK PATENT GMBH
Reel/Frame 025460/0814 →
Continuity (2)
Provisional Application 61067492 · Feb 28, 2008
Related Publication 20110053906A1 · Mar 3, 2011