HIV INHIBITING PYRIMIDINES DERIVATIVES

This invention concerns HIV replication inhibitors of formula (I) the N- oxides, the pharmaceutically acceptable addition salts, the quaternary amine s and the stereochemically isomeric forms thereof, wherein the ring containing - a1=a2-a3=a4- and -b1=b2-b3=b4- represents phenyl, pyridyl, pyrimidiny...

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Main Authors DE JONGE, MARC RENE, VINKERS, HENDRIK MAARTEN, JANSSEN, PAUL ADRIAAN JAN, PALANDJIAN, PATRICE, DAEYAERT, FREDERIK FRANS DESIRE, HEERES, JAN, KOYMANS, LUCIEN MARIA HENRICUS, GUILLEMONT, JEROME EMILE GEORGES, VAN AKEN, KOEN JEANNE ALFONS, LEWI, PAULUS JOANNES
Format Patent
LanguageEnglish
French
Published 27.02.2003
Edition7
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Abstract This invention concerns HIV replication inhibitors of formula (I) the N- oxides, the pharmaceutically acceptable addition salts, the quaternary amine s and the stereochemically isomeric forms thereof, wherein the ring containing - a1=a2-a3=a4- and -b1=b2-b3=b4- represents phenyl, pyridyl, pyrimidinyl, pirazinyl, pyridazinyl;n is 0 to 5; m is 1 to 4; R1 is hydrogen; aryl; formy l; C1-6alkylcarbonyl; C1-6alkyl; C1-6alkyloxycarbonyl, substituted C1-6alkyl, C 1- 6alkylcarbonyl; R2 is hydroxy, halo, optionally substituted C1-6alkyl, C3- 7cycloalkyl, optionally substituted C2-6alkenyl, optionally substituted C2- 6alkynyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, -S(=O)pR6, -NH-S(=O)pR6, -C(=O)R6, -NHC(=O)H, -C(=O)NHNH 2, -NHC(=O)R6, -C(=NH)R6 or a 5-membered heterocycle; X1 is -NR5-, -NH-NH-, -N= N- , -O-, -C(=O)-, C1-4alkanediyl, -CHOH-, -S-, -S(=O)p-, -X2-C1-4alkanediyl- o r - C1-4alkanediyl-X2-; R3 is NHR13; NR13R14; -C(=O)-NHR13; -C(=O)-NR13R14; -C(= O)- R15; -CH=N-NH-C(=O)-R16; substituted C1-6alkyl; optionally substituted C1- 6alkyloxyC1-6alkyl; substituted C2-6alkenyl; substituted C2-6alkynyl; C1- 6alkyl substituted with hydroxy and a second substituent; -C(=N-O-R8)-C1- 4alkyl; R7; or -X3-R7; R4 ishalo, hydroxy, C1-6alkyl, C3-7cycloalkyl, C1- 6alkyloxy, cyano, nitro, polyhaloC1-6alkyl, polyhaloC1-6alkyloxy, aminocarbonyl, C1-6alkyloxycarbonyl, C1-6alkylcarbonyl, formyl, amino, mono- or di(C1-4alkyl)amino; their use as a medicine, their processes for preparation and pharmaceutical compositions comprising them.
AbstractList This invention concerns HIV replication inhibitors of formula (I) the N- oxides, the pharmaceutically acceptable addition salts, the quaternary amine s and the stereochemically isomeric forms thereof, wherein the ring containing - a1=a2-a3=a4- and -b1=b2-b3=b4- represents phenyl, pyridyl, pyrimidinyl, pirazinyl, pyridazinyl;n is 0 to 5; m is 1 to 4; R1 is hydrogen; aryl; formy l; C1-6alkylcarbonyl; C1-6alkyl; C1-6alkyloxycarbonyl, substituted C1-6alkyl, C 1- 6alkylcarbonyl; R2 is hydroxy, halo, optionally substituted C1-6alkyl, C3- 7cycloalkyl, optionally substituted C2-6alkenyl, optionally substituted C2- 6alkynyl, C1-6alkyloxy, C1-6alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C1-6alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, -S(=O)pR6, -NH-S(=O)pR6, -C(=O)R6, -NHC(=O)H, -C(=O)NHNH 2, -NHC(=O)R6, -C(=NH)R6 or a 5-membered heterocycle; X1 is -NR5-, -NH-NH-, -N= N- , -O-, -C(=O)-, C1-4alkanediyl, -CHOH-, -S-, -S(=O)p-, -X2-C1-4alkanediyl- o r - C1-4alkanediyl-X2-; R3 is NHR13; NR13R14; -C(=O)-NHR13; -C(=O)-NR13R14; -C(= O)- R15; -CH=N-NH-C(=O)-R16; substituted C1-6alkyl; optionally substituted C1- 6alkyloxyC1-6alkyl; substituted C2-6alkenyl; substituted C2-6alkynyl; C1- 6alkyl substituted with hydroxy and a second substituent; -C(=N-O-R8)-C1- 4alkyl; R7; or -X3-R7; R4 ishalo, hydroxy, C1-6alkyl, C3-7cycloalkyl, C1- 6alkyloxy, cyano, nitro, polyhaloC1-6alkyl, polyhaloC1-6alkyloxy, aminocarbonyl, C1-6alkyloxycarbonyl, C1-6alkylcarbonyl, formyl, amino, mono- or di(C1-4alkyl)amino; their use as a medicine, their processes for preparation and pharmaceutical compositions comprising them.
Author HEERES, JAN
KOYMANS, LUCIEN MARIA HENRICUS
LEWI, PAULUS JOANNES
VAN AKEN, KOEN JEANNE ALFONS
GUILLEMONT, JEROME EMILE GEORGES
VINKERS, HENDRIK MAARTEN
PALANDJIAN, PATRICE
DAEYAERT, FREDERIK FRANS DESIRE
JANSSEN, PAUL ADRIAAN JAN
DE JONGE, MARC RENE
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– fullname: DAEYAERT, FREDERIK FRANS DESIRE
– fullname: HEERES, JAN
– fullname: KOYMANS, LUCIEN MARIA HENRICUS
– fullname: GUILLEMONT, JEROME EMILE GEORGES
– fullname: VAN AKEN, KOEN JEANNE ALFONS
– fullname: LEWI, PAULUS JOANNES
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DocumentTitleAlternate DERIVES DE PYRIMIDINES INHIBITEURS DE VIH
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Snippet This invention concerns HIV replication inhibitors of formula (I) the N- oxides, the pharmaceutically acceptable addition salts, the quaternary amine s and the...
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SubjectTerms ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
Title HIV INHIBITING PYRIMIDINES DERIVATIVES
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