IP Library Granted Patent US 7,795,248
Granted Patent B2
US 7,795,248 · App. 11/432,931 · Granted Sep 14, 2010

Substituted 7,8-dihydro-1H-pyrimido[4,5-B][1,4]diazepin-4-amines are novel kinase inhibitors

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Quick Facts
Patent No.
US 7,795,248
App. No.
11/432,931
Granted
Sep 14, 2010
Kind
B2
Abstract

Compounds having the Formula (I) are useful for inhibiting protein tyrosine kinases. The present invention also discloses methods of making the compounds, compositions containing the compounds, and methods of treatment using the compounds.

Claims (53)

1. A compound of Formula (I)

or a therapeutically acceptable salt thereof, wherein

R 1 is selected from the group consisting of hydrogen and NH 2 ;

R 2 is selected from the group consisting of hydrogen, alkoxycarbonyl, alkyl, alkylcarbonyl, arylalkoxycarbonyl, and heterocyclealkyl;

A is selected from the group consisting of phenyl and pyridinyl;

L is selected from the group consisting of —(CH 2 ) n N(R 3 )C(O)—, —N(R 3 )C(O)(CH 2 ) n —, and —(CH 2 ) n N(R 3 )C(O)N(R 4 )—;

n is 0, 1, 2, 3, 4, 5 or 6;

R 3 and R 4 are independently selected from the group consisting of hydrogen and alkyl;

R 5 is independently selected from the group consisting of alkenyl, alkoxy, alkoxycarbonyl, alkyl, alkynyl, haloalkoxy, haloalkyl, halogen, hydroxy, hydroxyalkyl, and NR A R B ;

m is 0, 1, 2, 3, or 4;

R 6 is selected from the group consisting of aryl, arylalkenyl, arylalkyl, cycloalkyl, cycloalkylalkenyl, cycloalkylalkyl, heteroaryl, heteroarylalkenyl, heteroarylalkyl, heterocycle, heterocyclealkenyl, and heterocyclealkyl; and

R A and R B are independently selected from the group consisting of hydrogen and alkyl.

2. The compound according to claim 1 wherein

A is phenyl;

L is —(CH 2 ) n N(R 3 )C(O)N(R 4 )—; and

R 6 is aryl.

3. The compound according to claim 1 wherein

R 1 , R 2 , R 3 , and R 4 are each hydrogen;

m is 0;

A is phenyl;

L is —(CH 2 ) n N(R 3 )C(O)N(R 4 )—;

n is 0; and

R 6 is aryl wherein the aryl is phenyl optionally substituted with 1 or 2 substituents selected from the group consisting of alkyl, haloalkyl, and halogen.

4. The compound according to claim 1 wherein

R 1 , R 2 , R 3 , and R 4 are each hydrogen;

m is 1;

R 5 is alkyl;

A is phenyl;

L is —(CH 2 ) n N(R 3 )C(O)N(R 4 )—;

n is 0; and

R 6 is aryl wherein the aryl is phenyl optionally substituted with 1 or 2 substituents selected from the group consisting of alkyl, haloalkyl, and halogen.

5. The compound according to claim 1 wherein

A is phenyl;

L is —(CH 2 ) n N(R 3 )C(O)—; and

R 6 is arylalkenyl.

6. The compound according to claim 1 selected from the group consisting of

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-phenylurea;

N-[3-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-phenylurea;

N-[3-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-[3-(trifluoromethyl)phenyl]urea;

N-[3-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-(4-fluoro-3-methylphenyl)urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-[3-(trifluoromethyl)phenyl]urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-(2-fluoro-5-methylphenyl)urea;

N-[5-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)-2-methylphenyl]-N′-[3-(trifluoromethyl)phenyl]urea;

N-[5-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)-2-methylphenyl]-N′-(2-fluoro-5-methylphenyl)urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-[2-fluoro-5-(trifluoromethyl)phenyl]urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-[4-chloro-3-(trifluoromethyl)phenyl]urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-(3-chlorophenyl)urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-[4-fluoro-3-(trifluoromethyl)phenyl]urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-(3-bromophenyl)urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-[4-(trifluoromethyl)phenyl]urea;

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-N′-[2-fluoro-3-(trifluoromethyl)phenyl]urea; and

N-[4-(4-amino-8,9-dihydro-7H-pyrimido[4,5-b][1,4]diazepin-6-yl)phenyl]-3-[3-(trifluoromethyl)phenyl]acrylamide.

7. A pharmaceutical composition comprising a compound of claim 1 or a therapeutically acceptable salt thereof, in combination with a therapeutically acceptable carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2013
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 030185/0141 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2006
From: GRACIAS, VIJAYA J.; ABAD-ZAPATERO, CELERINO; DJURIC, STEVAN W.; JI, ZHIQIN; MICHAELIDES, MICHAEL R.; STEWART, KENT D.; ZANZE, IRINI
To: ABBOTT LABORATORIES
Reel/Frame 018049/0668 →