http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102816200-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J43-00
filingDate 2012-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5f5e09aebf448dacc7ce359320a794a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6037c5726899d3ba6f011f5a1df24988
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publicationDate 2015-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102816200-B
titleOfInvention Method for preparing abiraterone acetate
abstract The invention discloses a convenient, rapid and economical method for massively preparing abiraterone acetate. According to the method, dehydroepiandrosterone acetate is used as a starting material, a keto carbonyl group is converted to hydrazone, and the abiraterone acetate is directly synthesized through iodination and Suzuki coupling reaction. According to the method, the operation is simple and convenient, the total yield of the three-step reaction is 34.7%, the product purity is 98.5%, the column chromatography separation purification is not required in the postprocessing, and the method is suitable for industrial production.
priorityDate 2012-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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