IP Library Granted Patent US 8,399,483
Granted Patent B2
US 8,399,483 · App. 12/809,394 · Granted Mar 19, 2013

Quinoxaline and quinoline derivatives as kinase inhibitors

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Quick Facts
Patent No.
US 8,399,483
App. No.
12/809,394
Granted
Mar 19, 2013
Kind
B2
Abstract

A series of heteroaryl-substituted quinoxaline and quinoline derivatives, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions, said substituted derivatives having the general formula

Claims (24)

1. A compound of formula (IA) or an N-oxide thereof, or a pharmaceutically acceptable salt thereof:

wherein

Alk 1 represents a straight or branched C 1-3 alkylene chain;

L 1 represents NR 9 ;

Y represents pyrrolyl, pyridin-2-yl, pyridin-3-yl, indolyl, isoquinolinyl, imidazolyl, pyrazolyl, triazolyl, pyridazinyl, pyrimidin-5-yl, pyrazinyl, triazinyl, indazolyl, furopyridinyl, benzoxazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, purin-1-yl, purin-2-yl, purin-3-yl, purin-7-yl, purin-8-yl, pyrazolo[3,4-d]pyrimidin-4-yl, triazolopyrimidinyl, naphthyridinyl, pteridinyl or pyridopyrimidin-4-yl, any of which groups may be optionally substituted by one, two or three substituents independently selected from halogen, cyano, nitro, C 1-6 alkyl, trifluoromethyl, hydroxy, C 1-6 alkoxy, difluoromethoxy, trifluoromethoxy, C 1-6 alkylthio, C 1-6 alkylsulfinyl, C 1-6 alkylsulfonyl, amino, C 1-6 alkylamino, di(C 1-6 )alkylamino, C 2-6 alkylcarbonylamino, C 1-6 alkylsulfonylamino, formyl, C 2-6 alkylcarbonyl, C 3-6 cycloalkylcarbonyl, C 3-6 heterocycloalkylcarbonyl, carboxy, C 2-6 alkoxycarbonyl, aminocarbonyl, C 1-6 alkylaminocarbonyl, di(C 1-6 )alkylaminocarbonyl, aminosulfonyl, C 1-6 alkylaminosulfonyl, di(C 1-6 )alkylaminosulfonyl, oxo and arylamino;

R 1 , R 2 and R 3 independently represent hydrogen, halogen, cyano, nitro, C 1-6 alkyl, trifluoromethyl, aryl(C 1-6 )alkyl, hydroxy, C 1-6 alkoxy, difluoromethoxy, trifluoromethoxy, C 1-6 alkylthio, C 1-6 alkylsulfinyl, C 1-6 alkylsulfonyl, amino, C 1-6 alkylamino, di(C 1-6 )alkyl-amino, C 2-6 alkylcarbonylamino, C 2-6 alkoxycarbonylamino, C 1-6 alkylsulfonylamino, formyl, C 2-6 alkylcarbonyl, carboxy, C 2-6 alkoxycarbonyl, aminocarbonyl, C 1-6 alkylaminocarbonyl, di(C 1-6 )alkylaminocarbonyl, aminosulfonyl, C 1-6 alkylaminosulfonyl or di(C 1-6 )alkylaminosulfonyl;

R 4 represents a group of formula (a):

in which represents the bond attaching the ring A to the rest of the molecule;

A represents a monocyclic aryl or heteroaryl group;

R 5 , R 6 and R 7 independently represent hydrogen, halogen, cyano, nitro, C 1-6 alkyl, trifluoromethyl, hydroxy, C 1-6 alkoxy, difluoromethoxy, trifluoromethoxy, C 1-6 alkylthio, C 1-6 alkylsulfinyl, C 1-6 alkylsulfonyl, amino, C 1-6 alkylamino, di(C 1-6 )alkylamino, C 2-6 alkylcarbonylamino, C 2-6 alkoxycarbonylamino, C 1-6 alkylsulfonylamino, formyl, C 2-6 alkylcarbonyl, carboxy, C 2-6 alkoxycarbonyl, aminocarbonyl, C 1-6 alkylaminocarbonyl, di(C 1-6 )alkylaminocarbonyl, aminosulfonyl, C 1-6 alkylaminosulfonyl, di(C 1-6 )alkylamino-sulfonyl, C 3-7 cycloalkyl or C 3-6 heterocycloalkyl, or optionally substituted monocyclic aryl or heteroaryl;

R 8 represents hydrogen, halogen, C 1-6 alkyl or C 1-6 alkoxy; and

R 9 represents hydrogen or C 1-6 alkyl.

2. A compound as claimed in claim 1 , wherein Y represents isoquinolinyl, triazinyl, purin-3-yl, purin-7-yl, or pyridopyrimidin-4-yl, any of which groups may be optionally substituted by one, two or three substituents.

3. A compound as claimed in claim 1 wherein Y represents optionally substituted triazinyl.

4. A compound as claimed in claim 1 or an N-oxide thereof, or a pharmaceutically acceptable salt thereof, wherein

Y represents pyridopyrimidin-4-yl, which may be optionally substituted by one, two or three substituents.

5. A compound as claimed in claim 1 wherein R 8 represents hydrogen.

6. A compound as claimed in claim 1 wherein R 9 represents hydrogen.

7. A compound as claimed in claim 1 wherein Alk 1 represents —CH 2 —, —CH(CH 3 )— or —CH(CH 2 CH 3 )—.

8. A compound as claimed in claim 7 wherein Alk 1 represents —CH(CH 3 )—.

9. A compound as claimed in claim 1 wherein the moiety A represents phenyl, pyrrolyl, furyl, thienyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, triazolyl, oxadiazolyl, thiadiazolyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, tetrazolyl or triazinyl.

10. A compound as claimed in claim 9 wherein the moiety A represents phenyl.

11. A compound as claimed in claim 9 wherein the moiety A represents pyridinyl.

12. A pharmaceutical composition comprising a compound of formula (IA) as claimed in claim 1 or an N-oxide thereof, or a pharmaceutically acceptable salt thereof, in association with a pharmaceutically acceptable carrier.

Assignments (2)
CONFIRMATORY ASSIGNMENT Recorded Jun 10, 2016
From: UCB PHARMA, S.A.
To: UCB BIOPHARMA SPRL
Reel/Frame 038953/0312 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2011
From: ALLEN, DANIEL REES; BUCKLEY, GEORGE MARTIN; BURLI, ROLAND; DAVENPORT, JOHN RICHARD; KINSELLA, NATASHA; RATCLIFFE, ANDREW JAMES; RICHARD, MARIANNA DILANI; SABIN, VERITY MARGARET; SHARPE, ANDREW; TAIT, LAURA JANE; WARRELLOW, GRAHAM JOHN; WILLIAMS, SOPHIE CAROLINE; LOCK, CHRISTOPHER JAMES; LOWE, CHRISTOPHER; PITT, WILLIAM ROSS; MACK, STEPHEN ROBERT
To: UCB PHARMA S.A.
Reel/Frame 026000/0759 →