2,4, (4,6) PYRIMIDINE DERIVATIVES

The present invention concerns the compounds of formula (I), the N-oxide fonns, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein Z1 and Z2 represent NH; Y represents -C3_9alkyl-, -C3_9alkenyl-, -C1 -salkyl-NR 6- C1 -salkyl-, -C1_5alkyl-NR 7- CO-...

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Main Authors ROMBOUTS, FREDERIK JAN RITA, FREYNE, EDDY JEAN EDGARD, WILLEMS, MARC, VAN BRANDT, SVEN FRANCISCUS ANNA, EMBRECHTS, WERNER CONSTANT JOHAN, VAN EMELEN, KRISTOF
Format Patent
LanguageEnglish
Published 11.04.2019
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Abstract The present invention concerns the compounds of formula (I), the N-oxide fonns, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein Z1 and Z2 represent NH; Y represents -C3_9alkyl-, -C3_9alkenyl-, -C1 -salkyl-NR 6- C1 -salkyl-, -C1_5alkyl-NR 7- CO-C1 _ 5alkyl-, -C1-6alkyl-CO-NH-, -C1-6alkyl-NH-CO-, -C1 _2a lkyl-CO-H et10-CO-, -C1 _ 3alkyl-NH-CO-H et3-, -Het4-C1_3alkyl-CO-NH-C 1 _3alkyl-, -C1-2alkyl-NH-CO-L1- NH-, -NH-CO-L2-NH-, -C1-2 alkyl-CO-NH-L 3-CO-, -C1_2alkyl-NH-CO-L 1 -NH-CO- C1_3alkyl-, -C1 -2alkyl-CO-NH-L 3-CO-NH-C 1_3alkyl-, -C 1-2alkyl-NR 11 -CH2- CO-NH-C1_3alkyl-, Het5-CO-C1 -2alkyl-, -C1 _5alkyl-CO-NH-C 1 _3alkyl-CO-NH-, -C1 _5alkyl-NR 1 3-CO-C1 _3alkyl-NH-, -C1 _3alkyl-NH-CO-Het27- CO-, or -C1 _3alkyl-CO- Het28-CO-NH-?, X1 represents a direct bond, 0, -O-C1 _2alkyl-, -CO-C1 _2alkyl-, -NR16-C1 _2alkyl-, -CO- NR17-, Het23- C1 _2alkyl- or C1-2alkyl; X2 represents a direct bond, 0, -O-C1 _2alkyl-, -CO-C1 _2alkyl-, -NR18 -C1 _2alkyl-, -CO- NR19-, Het24-C1-2alkyl- or C1-2alkyl; R1 and R5 each independently represent hydrogen, halo, C1_6alkyloxy- or C1 _6alkyloxy- substituted with Het1 or C1-4alkyloxy-; R2 and R4 each independently represent hydrogen or halo; R3 represents hydrogen or cyano; R6, R7, R1 3, R17 and R19 represent hydrogen; R11 represents hydrogen or C14 alkyl; R16 and R18 represent hydrogen, C14 a lkyl or Het17 -C14 alkyl-; L1 , L2 and L3 each independently represents C1 _8al kyl optionally substituted with one or where possible two or more substituents selected from phenyl, methylsulfide, cyano, polyhaloC1-4alkyl-phenyl-, C1-4alkyloxy, pyridinyl, mono- or di(C14 a lkyl)- amino- or C3_6cycloalkyl; Het1 , Het 2, Het 17 each independently represent morpholinyl, oxazolyl, isoxazolyl, or piperazinyl; Het3, Het 4, Het5 each independently represent morpholinyl, piperazinyl, piperidinyl or pyrrolidinyl; Het 1 0 represents piperazinyl, piperidinyl, pyrrolidinyl or azetidinyl; Het22 represents morpholinyl, oxazolyl, isoxazolyl or piperazinyl wherein said Het22 is optionally substituted with C14 a lkyl; Het23 and He t24 each independently represent a heterocycle selected from pyrrolidinyl, piperazinyl or piperidinyl wherein said Het23 or Het24 are optionally substituted with Het 22-carbonyl; Het 27 and Het28 each independently represent a heterocycle selected from morpholinyl, piperazinyl, piperidinyl or pyrrolidinyl.
AbstractList The present invention concerns the compounds of formula (I), the N-oxide fonns, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein Z1 and Z2 represent NH; Y represents -C3_9alkyl-, -C3_9alkenyl-, -C1 -salkyl-NR 6- C1 -salkyl-, -C1_5alkyl-NR 7- CO-C1 _ 5alkyl-, -C1-6alkyl-CO-NH-, -C1-6alkyl-NH-CO-, -C1 _2a lkyl-CO-H et10-CO-, -C1 _ 3alkyl-NH-CO-H et3-, -Het4-C1_3alkyl-CO-NH-C 1 _3alkyl-, -C1-2alkyl-NH-CO-L1- NH-, -NH-CO-L2-NH-, -C1-2 alkyl-CO-NH-L 3-CO-, -C1_2alkyl-NH-CO-L 1 -NH-CO- C1_3alkyl-, -C1 -2alkyl-CO-NH-L 3-CO-NH-C 1_3alkyl-, -C 1-2alkyl-NR 11 -CH2- CO-NH-C1_3alkyl-, Het5-CO-C1 -2alkyl-, -C1 _5alkyl-CO-NH-C 1 _3alkyl-CO-NH-, -C1 _5alkyl-NR 1 3-CO-C1 _3alkyl-NH-, -C1 _3alkyl-NH-CO-Het27- CO-, or -C1 _3alkyl-CO- Het28-CO-NH-?, X1 represents a direct bond, 0, -O-C1 _2alkyl-, -CO-C1 _2alkyl-, -NR16-C1 _2alkyl-, -CO- NR17-, Het23- C1 _2alkyl- or C1-2alkyl; X2 represents a direct bond, 0, -O-C1 _2alkyl-, -CO-C1 _2alkyl-, -NR18 -C1 _2alkyl-, -CO- NR19-, Het24-C1-2alkyl- or C1-2alkyl; R1 and R5 each independently represent hydrogen, halo, C1_6alkyloxy- or C1 _6alkyloxy- substituted with Het1 or C1-4alkyloxy-; R2 and R4 each independently represent hydrogen or halo; R3 represents hydrogen or cyano; R6, R7, R1 3, R17 and R19 represent hydrogen; R11 represents hydrogen or C14 alkyl; R16 and R18 represent hydrogen, C14 a lkyl or Het17 -C14 alkyl-; L1 , L2 and L3 each independently represents C1 _8al kyl optionally substituted with one or where possible two or more substituents selected from phenyl, methylsulfide, cyano, polyhaloC1-4alkyl-phenyl-, C1-4alkyloxy, pyridinyl, mono- or di(C14 a lkyl)- amino- or C3_6cycloalkyl; Het1 , Het 2, Het 17 each independently represent morpholinyl, oxazolyl, isoxazolyl, or piperazinyl; Het3, Het 4, Het5 each independently represent morpholinyl, piperazinyl, piperidinyl or pyrrolidinyl; Het 1 0 represents piperazinyl, piperidinyl, pyrrolidinyl or azetidinyl; Het22 represents morpholinyl, oxazolyl, isoxazolyl or piperazinyl wherein said Het22 is optionally substituted with C14 a lkyl; Het23 and He t24 each independently represent a heterocycle selected from pyrrolidinyl, piperazinyl or piperidinyl wherein said Het23 or Het24 are optionally substituted with Het 22-carbonyl; Het 27 and Het28 each independently represent a heterocycle selected from morpholinyl, piperazinyl, piperidinyl or pyrrolidinyl.
Author EMBRECHTS, WERNER CONSTANT JOHAN
VAN EMELEN, KRISTOF
VAN BRANDT, SVEN FRANCISCUS ANNA
ROMBOUTS, FREDERIK JAN RITA
FREYNE, EDDY JEAN EDGARD
WILLEMS, MARC
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– fullname: EMBRECHTS, WERNER CONSTANT JOHAN
– fullname: VAN EMELEN, KRISTOF
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Snippet The present invention concerns the compounds of formula (I), the N-oxide fonns, the pharmaceutically acceptable addition salts and the stereochemically...
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Title 2,4, (4,6) PYRIMIDINE DERIVATIVES
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