IP Library Granted Patent US 7,968,557
Granted Patent B2
US 7,968,557 · App. 10/589,099 · Granted Jun 28, 2011

Substituted pyrrolo[2,3-2]pyrimidines as protein kinase inhibitors

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Quick Facts
Patent No.
US 7,968,557
App. No.
10/589,099
Granted
Jun 28, 2011
Kind
B2
Abstract

The invention provides a novel class of compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with abnormal or deregulated kinase activity, particularly diseases or disorders that involve abnormal activation of the FAK, Abl, BCR-Abl, PDGF-R, c-Kit, NPM-ALK, Flt-3, JAK2 and c-Met kinases.

Claims (20)

1. A compound selected from Formula Ia and Id:

in which:

n is selected from 0, 1 and 2;

W is selected from —NR 4 —, —S—, —O—, —S(O)— and —S(O) 2 —; wherein R 4 is selected from hydrogen and C 1-6 alkyl;

R 1 is selected from C 6-10 aryl-C 0-4 alkyl, C 5-10 heteroaryl-C 0-4 alkyl, C 3-12 cycloalkyl-C 0-4 alkyl and C 3-8 heterocycloalkyl-C 0-4 alkyl; wherein any aryl, heteroaryl, cycloalkyl or heterocycloalkyl of R 1 is optionally substituted by 1 to 3 groups independently selected from halo, nitro, cyano, C 6-10 aryl, C 5-10 heteroaryl, C 3-12 cycloalkyl, C 3-8 heterocycloalkyl, C 1-6 alkyl, C 1-6 alkoxy, halo-substituted-C 1-6 alkyl, halo-substituted-C 1-6 alkoxy, —XNR 5 R 5 , —XNR 5 XNR 5 R 5 , —XNR 5 XOR 5 , —XOR 5 , —XSR 5 , —XS(O)R 5 , —XS(O) 2 R 5 , —XC(O)NR 5 R 5 , —XOXR 6 and —XC(O)R 6 ; wherein X is a bond or C 1-6 alkylene; R 5 is selected from hydrogen, C 1-6 alkyl and C 3-12 cycloalkyl-C 0-4 alkyl; and R 6 is selected from C 3-8 heterocycloalkyl-C 0-4 alkyl and C 5-10 heteroaryl -C 0-4 alkyl optionally substituted by 1 to 3 groups selected from C 1-6 alkyl and —C(O)OH; wherein any aryl, heteroaryl, cycloalkyl or heterocycloalkyl substituent of R 1 is further optionally substituted by 1 to 5 groups independently selected from C 1-6 alkyl and C 1-6 alkoxy;

R 2 is selected from C 6-10 aryl-C 0-4 alkyl, C 5-10 heteroaryl-C 0-4 alkyl, C 3-12 cycloalkyl -C 0-4 alkyl; wherein any arylalkyl, heteroarylalkyl, cycloalkylalkyl of R 2 is optionally substituted by 1 to 3 groups independently selected from halo, nitro, cyano, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, halo-substituted-C 1-6 alkyl, halo-substituted-C 1-6 alkoxy, C 3-8 heteroaryl C 0-4 alkyl, —XNR 5 R 5 , —XOR 5 , —XSR 5 , —XS(O)R 5 , —XS(O) 2 R 5 , —XSNR 5 R 5 , —XS(O)NR 5 R 5 , —XS(O) 2 NR 5 R 5 , —XC(O)OR 5 , —XOC(O)R 5 , —XC(O)R 5 , —XC(O)NR 5 XNR 5 R 5 , —XC(O)NR 5 R 5 , —XC(O)NR 5 XC(O)OR 5 , —XC(O)NR 5 XNR 5 C(O)R 5 , —XC(O)NR 5 XNR 5 C(O)OR 5 , —XC(O)NR 5 XOR 5 , —XC(O)N(XOR 5 ) 2 , —XNR 5 C(O)R 5 , —XC(O)NR 5 R 6 , —XC(O)R 6 , —XR 7 , —XC(O)R 7 , —XR 6 and —XC(O)NR 5 XR 7 ; wherein X is a bond or C 1-6 alkylene; and R 5 is selected from hydrogen, C 1-6 alkyl and C 3-12 cycloalkyl-C 0-4 alkyl; R 6 is selected from C 3-8 heterocycloalkyl-C 0-4 alkyl and C 5-10 heteroaryl-C 0-4 alkyl optionally substituted by 1 to 3 groups selected from C 1-6 alkyl and —C(O)OH; and R 7 is selected from halo and cyano;

R 3 is selected from halo, hydroxy, —XSR 5 , —XS(O)R 5 , —XS(O) 2 R 5 , —XC(O)R 5 and —XC(O)OR 5 ; wherein X is a bond or C 1-6 alkylene; and R 5 is selected from hydrogen, C 1-6 alkyl and C 3-12 cycloalkyl-C 0-4 alkyl; or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 in which:

W is selected from —NR 4 — and —O—; wherein R 4 is selected from hydrogen and C 1-6 alkyl;

R 1 is selected from C 6-10 aryl-C 0-4 alkyl and C 5-10 heteroaryl-C 0-4 alkyl; wherein any aryl and heteroaryl of R 1 is optionally substituted by 1 to 3 groups independently selected from halo, nitro, C 5-10 heteroaryl, C 1-6 alkyl, C 1-6 alkoxy, halo-substituted-C 1-6 alkyl, —XNR 5 R 5 , —XOR 5 , —XSR 5 , —XNR 5 XNR 5 R 5 , —XNR 5 XOR 5 , —XC(O)NR 5 R 5 , —XOXR 6 and —XC(O)R 6 ; wherein X is a bond or C 1-6 alkylene; R 5 is selected from hydrogen, C 1-6 alkyl and C 3-12 cycloalkyl-C 0-4 alkyl; and R 6 is selected from C 3-8 heterocycloalkyl-C 0-4 alkyl and C 5-10 heteroaryl -C 0-4 alkyl optionally substituted by 1 to 3 groups selected from C 1-6 alkyl and —C(O)OH; wherein any heteroaryl substituent of R 1 is further optionally substituted by 1 to 5 C 1-6 alkyl groups;

R 2 is selected from C 6-10 aryl-C 0-4 alkyl and C 5-10 heteroaryl-C 0-4 alkyl; wherein any arylalkyl or heteroarylalkyl of R 2 is optionally substituted by 1 to 3 groups independently selected from halo, nitro, cyano, C 1-6 alkyl, C 2-6 alkenyl, C 1-6 alkoxy, halo-substituted-C 1-6 alkyl, C 3-8 heteroarylC 0-4 alkyl, —XNR 5 R 5 , —XOR 5 , —XSR 5 , —XS(O) 2 NR 5 R 5 , —XC(O)OR 5 , —XOC(O)R 5 , —XC(O)NR 5 XNR 5 R 5 , —XC(O)NR 5 XC(O)OR 5 , —XC(O)NR 5 XNR 5 C(O)R 5 , —XC(O)NR 5 XNR 5 C(O)OR 5 , —XC(O)NR 5 XOR 5 , —XC(O)N(XOR 5 ) 2 , —XNR 5 C(O)R 5 , —XC(O)NR 5 R 6 , —XC(O)R 6 , —XR 7 , —XR 6 and —XC(O)NR 5 XR 7 ; wherein X is a bond or C 1-6 alkylene; and R 5 is selected from hydrogen, C 1-6 alkyl and C 3-12 cycloalkyl-C 0-4 alkyl; R 6 is selected from C 3-8 heterocycloalkyl-C 0-4 alkyl and C 5-10 heteroaryl-C 0-4 alkyl optionally substituted by 1 to 3 groups selected from C 1-6 alkyl and —C(O)OH; and R 7 is cyano; and

R 3 is selected from halo, hydroxy, —XC(O)R 5 and —XC(O)OR 5 ; wherein X is a bond or C 1-6 alkylene; and R 5 is selected from hydrogen, C 1-6 alkyl and C 3-12 cycloalkyl-C 0-4 alkyl; or a pharmaceutically acceptable sale thereof.

3. The compound of claim 1 in which W is selected from —NH— and —O—; and R 1 is selected from phenyl, benzyl, 5,6,7,8-tetrahydro-naphthalenyl, benzo[1,3]dioxolyl, 1H-indazol-7-yl, indan-4-yl and 1H-indolyl; wherein any R 1 is optionally substituted by 1 to 3 groups independently selected from methoxy, methyl, amino, halo, hydroxymethyl, hydroxy, quinoxalinyl, ethyl, pyridinyl, methoxy-phenyl, piperazinyl-carbonyl, 2-(4-methyl-piperazin-1-yl)-ethoxy, isopropyl, methyl-sulfanyl, tri-fluoro-methyl, ethoxy, 3-isopropylamino-propylamino, dimethyl-amino, morpholino, cyclopropyl-methoxy, butoxy, cycloheptyl-oxy and 1,4,5,7-tetramethyl-pyrrolo[3,4-d]pyridazinyl; or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 in which R 2 is selected from pyridinyl, phenyl, thiazolyl, pyridinyl-methyl, pyridinyl-ethyl, thiophenyl, benzyl, quinolinyl, 7-oxo-5,6,7,8-tetrahydro-naphthalenyl, naphthyl and pyrimidinyl; wherein any arylalkyl or heteroarylalkyl of R 2 is optionally substituted by 1 to 3 groups independently selected from halo, nitro, cyano, methyl, propyl-sulfamoyl, methyl-sulfamoyl, methoxy, methyl-carboxy, carboxy, amino, cyano-ethyl, cyano-methyl, ethenyl, tri-fluoro-methyl, hydroxy-methyl, ethyl, methyl-sulfanyl, butyl, isobutyl, carboxy-methyl-formamidyl, 1-carboxy-ethyl-formamidyl, carboxy-ethyl, amino-ethyl-formamidyl, amino-propyl-formamidyl, dimethyl-amino-ethyl-formamidyl, dimethyl-amino-propyl-formamidyl, dimethyl-amino-butyl-formamidyl, methyl-formamidyl, ethyl-formamidyl, ethyl-formamidyl-methyl, N-(2-(dimethylamino)ethyl)-3-phenylpropanamide, 2-(2-dimethylamino-formamidyl)-ethyl, 2-(amino-ethyl-formamidyl)-ethyl, 2-(amino-propyl-formamidyl) -ethyl, 2-(propyl-formamidyl)-ethyl, amino-propyl-formamidyl-methyl, morpholino-ethyl-formamidyl, morpholino-carbonyl-methyl, amino-ethyl-formamidyl-methyl, cyclobutyl-formamidyl, methyl -formamidyl-methyl, dimethyl-formamidyl-methyl, hydroxy-ethyl-formamidyl-methyl, hydroxy-propyl -formamidyl-methyl, N,N-bis-(3-hydroxy-propyl)-formamidyl, cyclopentyl-formamidyl, isobutyl-formamidyl, isobutyl-formamidyl-methyl, cyclopentyl-formamidyl-methyl, cyano-ethyl-formamidyl, cyano-methyl-formamidyl, pyrrolidinyl-ethyl-formamidyl, 2-(isobutyl-formamidyl)-ethyl, 1H-tetrazolyl, 2-(1H-tetrazol-5-yl)-ethyl, 2-(1H-tetrazol-5-yl)-methyl, 2-(1-methyl-1H-tetrazol-5-yl) -methyl, acetyl-amino, cyclopropyl-formamidyl-methyl, hydroxy-ethyl-formamidyl, hydroxy-propyl-formamidyl, propyl-formamidyl-methyl, ethoxy-propyl-formamidyl, acetyl-amino-ethyl-formamidyl, 1-methyl-piperidin-4-yl-formamidyl, morpholino-carbonyl-ethyl, methoxy-carbonyl-methyl, methoxy-carbonyl-ethyl-formamidyl, methoxy-carbonyl-ethyl-formamidyl-methyl, methoxy-carbonyl-methyl-formamidyl-methyl, methoxy-carbonyl-methyl-formamidyl, acetyl-amino-ethyl-formamidyl-methyl, ethoxy-propyl-formamidyl-methyl, methoxy-carbonyl-ethyl, 1-formyl -pyrrolidin-2-yl-carboxylic acid, (1-carboxy-3-methyl-butyl)-formamidyl, 2-(methoxy-carbonyl-methyl-formamidyl)-ethyl, 1-carboxy-(2,2-dimethyl-propyl)-formamidyl, 3-tert-butoxycarbonyl-amino-propyl-formamidyl, acetoxy-methyl and 1-carboxy-ethyl-formamidyl; or a pharmaceutically acceptable salt thereof.

5. The compound of claim 1 in which n is 0 or 1; and R 3 is selected from halo, hydroxy, —C(O)OH and —C(O)OCH 3 ; or a pharmaceutically acceptable salt thereof.

6. The compound of claim 1 of Formula Ig:

in which R 2 is selected from pyridinyl, phenyl, thiazolyl, pyridinyl-methyl, pyridinyl-ethyl, thiophenyl, benzyl, quinolinyl, 7-oxo-5,6,7,8-tetrahydro-naphthalenyl, naphthyl and pyrimidinyl;

wherein any arylalkyl or heteroarylalkyl of R 2 is optionally substituted by 1 to 3 groups independently selected from halo, nitro, cyano, methyl, propyl-sulfamoyl, methyl-sulfamoyl, methoxy, methyl-carboxy, 2-dimethylamino-ethyl-formamyl, carboxy, amino, cyano-ethyl, cyano-methyl, ethenyl, tri-fluoro-methyl, hydroxy-methyl, ethyl, methyl-sulfanyl, butyl, isobutyl, carboxy-methyl-formamidyl, 1-carboxy-ethyl-formamidyl, carboxy-ethyl, amino-ethyl-formamidyl, amino-propyl-formamidyl, dimethyl-amino-ethyl-fornnamidyl, dimethyl-amino-propyl-formamidyl, dimethyl-amino-butyl-formamidyl, methyl-formamidyl, ethyl-formamidyl, ethyl-formamidyl-methyl, N-(2-(dimethylamino)ethyl)-3-phenylpropanaide, 2-(2-dimethylamino-formamidyl)-ethyl, 2-(amino -ethyl-formamidyl)-ethyl, 2-(amino-propyl-formamidyl)-ethyl, 2-(propyl-formamidyl)-ethyl, amino- propyl-formamidyl-methyl, morpholino-ethyl-formamidyl, morpholino-carbonyl-methyl, amino-ethyl-formamidyl-methyl, cyclobutyl-formamidyl, methyl-formamidyl-methyl, dimethyl-formamidyl-methyl, hydroxy-ethyl -formamidyl-methyl, hydroxy-propyl-formamidyl-methyl, N,N-bis-(3-hydroxy-propyl)-formamidyl, cyclopentyl-formamidyl, isobutyl-formamidyl, isobutyl-formamidyl-methyl, cyclopentyl-formamidyl-methyl, cyano-ethyl-formamidyl, cyano-methyl-formamidyl, pyrrolidinyl-ethyl -formamidyl, 2-(isobutyl-formamidyl)-ethyl, 1 H-tetrazolyl, 2-(1H-tetrazol-5-yl)-ethyl, 2-(1H-tetrazol -5-yl)-methyl, 2-(1-methyl-1H-tetrazol-5-yl)-methyl, acetyl-amino, cyclopropyl-formamidyl-methyl, hydroxy-ethyl-fornnannidyl, hydroxy-propyl-formamidyl, propyl-formamidyl-methyl, ethoxy-propyl -formamidyl, acetyl-amino-ethyl-formamidyl, 1-methyl-piperidin-4-yl-formamidyl, morpholino -carbonyl-ethyl, methoxy-carbonyl-methyl, methoxy-carbonyl-ethyl-formamidyl, methoxy -carbonyl-ethyl-formamidyl-methyl, methoxy-carbonyl-methyl-formamidyl-methyl, methoxy -carbonyl-methyl-formamidyl, acetyl-amino-ethyl-formamidyl-methyl, ethoxy-propyl-formamidyl-methyl, methoxy -carbonyl-ethyl, 1-formyl-pyrrolidin-2-yl-carboxylic acid, (1-carboxy-3-methyl-butyl)-formamidyl, 2-(methoxy-carbonyl-methyl-formamidyl)-ethyl, 1-carboxy-(2,2-dimethyl-propyl)-formamidyl, 3-tert -butoxycarbonyl-amino-propyl-formamidyl, acetoxy-methyl and 1-carboxy-ethyl-formamidyl; or a pharmaceutically acceptable salt thereof.

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

8. A compound selected from:

Assignments (4)
MERGER Recorded Apr 16, 2015
From: IRM LLC
To: NOVARTIS INTERNATIONAL PHARMACEUTICAL LTD.
Reel/Frame 035444/0397 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 16, 2015
From: NOVARTIS INTERNATIONAL PHARMACEUTICAL LTD.
To: NOVARTIS AG
Reel/Frame 035453/0224 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 12, 2007
From: CHOI, HA-SOON; WANG, ZHICHENG; GU, XIANG-JU; HE, XIAOHUI; HE, YUN; JIANG, TAO; LIU, YI; RICHMOND, WENDY; YANG, KUNYONG
To: IRM, LLC
Reel/Frame 020236/0361 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 12, 2007
From: GRAY, NATHANAEL S.; SIM, TAEBO
To: IRM, LLC
Reel/Frame 020360/0467 →