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filingDate 2017-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c27207e6faae0626c5b266039e591090
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publicationDate 2017-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106518832-A
titleOfInvention Preparation method of velpatasvir intermediate 9-bromine-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo [c,g] chromene-8(9h)-ketone
abstract The invention relates to a preparation method of a velpatasvir intermediate 9-bromine-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo [c,g] chromene-8(9h)-ketone. The compound is the key intermediate of velpatasvir. The preparation method is characterized in that a compound I is used as the raw material to react with 2-ethyleneoxy ethanol to obtain a compound II, the compound II is hydrolyzed under an acid condition to generate a compound III, and the compound III is brominated by tribromo pyridine to obtain the 9-bromine-3-(2-bromoacetyl)-10,11-dihydro-5H-dibenzo [c,g] chromene-8(9h)-ketone (intermediate A). The preparation method has the advantages that an original synthesizing route is shortened, and the method is stable in product quality, high in yield, simple in post-treatment and suitable for industrial production.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109020944-A
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type http://data.epo.org/linked-data/def/patent/Publication

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