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filingDate 1979-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bf9e28f7636eefd45d3cc4cab65c3a1
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publicationDate 1980-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0009683-A1
titleOfInvention Basic phenyl ethers, pharmaceutical compositions containing them and the preparation of these ethers and compositions
abstract G eine unsubstituierte oder eine ein- oder zweifach durch Halogen substituierte Phenyl- oder Benzylgruppe oder Alkyl mit 1 - 6 C-Atomen, Z -NR 1 R 2 , 1-lmidazolyl oder 2-Methyl-1-imidazolyl, A -CH=CR 3 , -CO-CHR 3 -, -CHOH-CHR 3 - oder -CH 2 -CHR 4 -, n 1, 2 oder 3, R 1 , R 2 und R 3 (gleich oder verschieden) jeweils H oder Alkyl mit 1 - 4 C-Atomen und R 4 Alkyl mit 1 - 4 C-Atomen nbedeuten, ninsbesondere z.B. 1-(4-p-Chlorphenoxy-phenyl)-3-(1-imidazolyl)-propen, sowie ihre physiologisch unbedenklichen Säureadditionssalze besitzen wertvolle pharmakologische, insbesondere antimykotische und antibakterielle Wirkungen. Es werden mehrere Arten zu ihrer Herstellung beschrieben.The new basic ethers of the general formula I wherein G is an unsubstituted or a mono- or disubstituted by halogen phenyl or benzyl group or alkyl with 1 - 6 C atoms, Z -NR 1 R 2 , 1-imidazolyl or 2-methyl-1-imidazolyl, A -CH = CR 3 , -CO-CHR 3 -, -CHOH-CHR 3 - or -CH 2 -CHR 4 -, n 1, 2 or 3, R 1 , R 2 and R 3 (identical or different) are each H or alkyl having 1 to 4 carbon atoms and R 4 alkyl with 1 - 4 carbon atoms mean, in particular 1- (4-p-chlorophenoxy-phenyl) -3- (1-imidazolyl) propene, in particular, and their physiologically acceptable acid addition salts have valuable pharmacological, in particular antifungal and antibacterial, effects. Several ways of making them are described.
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priorityDate 1978-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 1096.