http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HR-P20010161-B1

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filingDate 2001-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2009-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HR-P20010161-B1
titleOfInvention PYRIMIDINES WHICH INHIBIT HIV REPLICATION
abstract A compound of the formula N-oxides, addition salts, quaternary amines and stereochemically isomeric forms thereof, wherein 0 is 1, 1, 2, 3 or 4; R 1 is hydrogen, aryl, formyl, C 1-6 alkylcarbonyl, C 1-6 alkyl, C 1-6 alkyloxycarbonyl, C 1-6 alkyl substituted with formyl, C 1-6 alkylcarbonyl, C 1-6 alkyloxycarbonyl, C 1-6 -alkylcarbonyloxy; C1-6-alkyloxy-C1-6-alkylcarbonyl substituted with C1-6-alkyloxycarbonyl; R2a is cyano, aminocarbonyl, mono- or di (methyl) -aminocarbonyl, C1-6-alkyl substituted with cyano, amino-carbonyl or mono- or di- (methyl) aminocarbonyl, C2-6-alkenyl substituted with cyano, or C2- 6-alkynyl substituted with cyano; each R 2 independently represents hydroxy, halogen, C 1-6 alkyl optionally substituted with cyano or -C (= O) R 6, C 3-7 cycloalkyl, C 2-6 alkenyl optionally substituted with one or more halogen atoms or cyano, C2-6-alkynyl optionally substituted with one or more halogen atoms or cyano, C1-6-alkyloxy, C1-6-alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di (C1-6-alkyl) amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, -S (= O) PR6, -NH-S (= O) PR6, -C (= O) R6, -NHC (= O) H, -C (= O) NHNH2, -NHC (= O) R 6, -C (= NH) R 6 or a radical of formula wherein each A independently represents N, CH or CR 6, B is NH, O, S or NR 6, p is 1 or 2; iR6 is methyl, amino, mono- or dimethylamino or polyhalomethyl; L is C1-10-alkyl, C2-10-alkenyl, C2-10-alkynyl, C3-7-cycloalkyl, each of said aliphatic groups being substituted with one or two substituents independently selected from the group consisting of * C3- 7-cycloalkyl, * indolyl or isoindolyl, each optionally substituted with one, two, three or four substituents each independently selected from the group consisting of halogen, C1-6-alkyl, hydroxy, C1-6-alkyloxy, cyano, aminocarbonyl, nitro, amino, polyhalomethyl, polyhalo methyloxy and C1-6-alkylcarbonyl, * phenyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl, each of said aromatic rings being optionally substituted with one, two, three, four or five substituents each of which is independently selected from the substituents defined in R2; or L is -X-R3 wherein R3 represents phenyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl, each of said aromatic rings being optionally substituted with one, two, three, four or five substituents each independently selected from substituents defined by in R2; iX is -NR1-, -NH-NH-, -N = N-, -O-, -C (= O) -, -CHOH-, -S-, -S (= O) - or -S (= O) 2S; Q represents hydrogen, C1-6-alkyl, halogen, polyhalo-C1-6-alkyl or -NR4R5; iR4 and R5 are independently selected from the group consisting of hydrogen, hydroxy, C1-12-alkyl, C1-12-alkyloxy, C1-12-alkylcarbonyl, C1-12-alkyloxycarbonyl, aryl, amino, mono- or di (C1- 12-alkyl) amino, mono- or di (C1-12-alkyl) aminocarbonyl, wherein each of the abovementioned C1-12-alkyl groups may be optionally and individually substituted with one or two substituents, each of which is
priorityDate 1998-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 57.