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filingDate 2017-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20eef2fa44530043e63fd69b8eca04d0
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publicationDate 2019-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109810093-A
titleOfInvention A kind of preparation method of bilastine intermediate
abstract The invention belongs to the field of pharmaceutical preparations, and in particular relates to a preparation method of a bilastine intermediate, which is named 1-piperidinecarboxylic acid, 4-[1-(2-ethoxyethyl)-1H-benzimidazole -2-yl]-,1,1-dimethylethyl ester. The above-mentioned intermediate compound is generated by 2-(4-piperidine)-1H-benzimidazole after being protected by di-tert-butyl dicarbonate, and further reacted with 2-ethoxychloroethane. The above product is deprotected under acidic conditions and undergoes a substitution reaction to generate 1-(2-ethoxy-ethyl)-2-piperidine-4-yl-1H-benzimidazole. The preparation method of the new intermediate of bilastine provided by the invention provides a new way for the synthesis of bilastine. Purity, suitable for industrial scale production.
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type http://data.epo.org/linked-data/def/patent/Publication

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