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filingDate 2018-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0f327ca4cbded0def7249ab60a64f07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae1f6fadfb28448dda1f32a37437ee21
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publicationDate 2019-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109467535-A
titleOfInvention A kind of preparation method of fenbendazole
abstract The invention discloses a preparation method of fenbendazole. It is characterized in that: (1) using m-dibromobenzene as a starting material, through nitric acid/sulfuric acid system nitration reaction, to prepare intermediate 1 (2,4-dibromonitrobenzene); (2) using intermediate 1 as a raw material , through the ammoniation reaction that ammonia methanol solution participates in, prepares intermediate 2 (5-bromo-2-nitroaniline); (3) takes intermediate 2 and sodium thiophenolate solution as raw materials, through condensation reaction, prepares Intermediate 3 (4-phenylthio-2-nitroaniline); (4) Intermediate 3 is subjected to palladium-carbon catalytic hydrogenation reduction to generate intermediate 4 (4-phenylthio-1,2-phenylenediamine) ; (5) Intermediate 4 and methyl cyanamide formate aqueous solution, through cyclization reaction, generate product fenbendazole. The method is clean and environmentally friendly, with low production cost, product purity of more than 99.5%, and yield of not less than 84.0%.
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