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filingDate 1979-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91b19f41d2d78759df67e0d6dd8249f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bce128d7c65e095f5d27ff2506cab17d
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publicationDate 1980-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-143608-A5
titleOfInvention PROCESS FOR PREPARING 4'-SUBSTITUTED 2,4-DICHLOR-ALPHA- (IMIDAZOLE-N-YLMETHYL) -DIBENZYLAETHERNES
abstract The invention relates to a process for the preparation of novel 4-substituted 2,4-dichloro-α- (imidazol-N-ylmethyl) -dibenzyl ethers, including their salts, which have superior pharmacological effects, especially against pils, yeasts and bacteria, especially because of their lower toxicity compared to that of the known products. The invention relates to a process for the preparation of substituted 2,4-dichloro-a- (imidazol-N-ylmethyl) dibenzyläthern of the general formula I, wherein R is a phenyl or phenylthio radical, and their salts with acids, which characterized is' that in known per se 1- (2 ', 4' -Dichlorphenyi) -2- (imidazole-Ы-у1) -ethanol with a Halogenbenzylderivat, eg 4-chloromethyl-diphenyl or 1-bromomethyl-4-phenylthiobenzene is condensed in a solvent, where appropriate, the resulting 4'-substituted 2,4-dichloro-a- (imidazol-Ы-!! Methyl) -dibenzyl ether base of the general Formula I is converted into a salt with an acid. - Formula I
priorityDate 1978-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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