IP Library Granted Patent US 8,168,652
Granted Patent B2
US 8,168,652 · App. 13/255,757 · Granted May 1, 2012

Inhibitors of AKT activity

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Quick Facts
Patent No.
US 8,168,652
App. No.
13/255,757
Granted
May 1, 2012
Kind
B2
Abstract

The instant invention provides for substituted naphthyridine compounds that inhibit Akt activity. In particular, the compounds disclosed selectively inhibit one or two of the Akt isoforms. The invention also provides for compositions comprising such inhibitory compounds and methods of inhibiting Akt activity by administering the compound to a patient in need of treatment of cancer.

Claims (55)

1. A compound according to Formula A:

wherein:

R 1 is aryl, heteroaryl or heterocyclyl;

R 2 is a (C 1 -C 10 )alkyl or heterocyclyl which are optionally substituted with from one to three substituents selected from OH, O(C 1 -C 6 )alkyl, phenyl and heterocyclyl, wherein said phenyl is optionally substituted with from one to three substituents selected from OH; and

R 3 is a (C 1 -C 3 )alkyl or hydrogen;

or a pharmaceutically acceptable salt or a stereoisomer thereof.

2. A compound according to Formula A of claim 1 , wherein:

R 1 is aryl or heteroaryl;

R 2 is a (C 1 -C 10 )alkyl which is optionally substituted with from one to three substituents selected from OH, O(C 1 -C 6 )alkyl and phenyl, wherein said phenyl is optionally substituted with from one to three substituents selected from OH; and

R 3 is methyl or hydrogen;

or a pharmaceutically acceptable salt or a stereoisomer thereof.

3. A compound according to Formula A of claim 1 , wherein:

R 1 is 4-pyrazolyl;

R 2 is a (C 1 -C 10 )alkyl or heterocyclyl which are optionally substituted with from one to three substituents selected from OH, O(C 1 -C 6 )alkyl, phenyl and heterocyclyl, wherein said phenyl is optionally substituted with from one to three substituents selected from OH; and

R 3 is methyl or hydrogen;

or a pharmaceutically acceptable salt or a stereoisomer thereof.

4. A compound according to Formula A of claim 1 , wherein:

R 1 is 4-pyrazolyl;

R 2 is a (C 1 -C 10 )alkyl which is optionally substituted with from one to three substituents selected from OH, O(C 1 -C 6 )alkyl and phenyl, wherein said phenyl is optionally substituted with from one to three substituents selected from OH; and

R 3 is methyl or hydrogen;

or a pharmaceutically acceptable salt or a stereoisomer thereof.

5. A compound according to Formula A of claim 1 , wherein:

R 1 is 4-pyrazolyl;

R 2 is a (C 1 -C 10 )alkyl which is optionally substituted with from one to three substituents selected from OH and O(C 1 -C 6 )alkyl; and

R 3 is methyl or hydrogen;

or a pharmaceutically acceptable salt or a stereoisomer thereof.

6. A compound according to Formula A of claim 1 , wherein:

R 1 is 4-pyrazolyl;

R 2 is a (C 1 -C 10 )alkyl which is optionally substituted with from one to three substituents selected from OH and OCH 3 ; and

R 3 is methyl or hydrogen;

or a pharmaceutically acceptable salt or a stereoisomer thereof.

7. A compound which is selected from:

2,2-dimethyl-3-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino) propan-1-ol;

3-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)propan-1-ol;

{1-[({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)methyl]cyclobutyl}methanol;

{1-[({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)methyl]cyclopentyl}methanol;

{1-[({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)methyl]cyclohexyl}methanol;

4-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)butan-1-ol;

2,2-dimethyl-N-{4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}propan-1-amine;

2-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)ethanol;

[(1R,2S)-2-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino) cyclohexyl]methanol;

(2S)-1-methoxy-3-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)propan-2-ol;

1-[(2S)-1,4-dioxan-2-yl]-N-{4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}methanamine;

2-methyl-N-{4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}propan-1-amine;

1-cyclopropyl-N-{4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}methanamine;

N-{4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}cyclopentanamine;

[(1S,2R)-2-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino) cyclohexyl]methanol;

N-{4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}-1H-indol-5-amine;

3-[2-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)ethyl]phenol;

4-[2-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)ethyl]phenol;

4-[1-hydroxy-2-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino) propyl]phenol;

4-[(1R,2S)-1-hydroxy-2-({4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]benzyl}amino)propyl]phenol; and

(2,2-dimethyl-3-{[(1R)-1-{4-[3-phenyl-5-(1H-pyrazol-4-yl)-1,6-naphthyridin-2-yl]phenyl}ethyl]amino}propan-1-ol;

or a pharmaceutically acceptable salt or stereoisomer thereof.

8. A pharmaceutical composition comprising a pharmaceutical carrier, and dispersed therein, a therapeutically effective amount of a compound of claim 1 .

Assignments (2)
CHANGE OF NAME Recorded Aug 29, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028866/0511 →
MERGER Recorded Aug 27, 2012
From: MERCK SHARP & DOHME CORP.
To: SCHERING CORPORATION
Reel/Frame 028850/0515 →