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filingDate 2016-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_528210c4b468396601f8f483a821393f
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publicationDate 2018-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2018094014-A1
titleOfInvention Method of producing epirubicin and novel production intermediate thereof
abstract According to the present invention, it is possible to efficiently remove 13-dihydroepi-daunorubicin and 4′-epi-feudomycin, which are typical impurities possibly contained in 4′-epi-daunorubicin as a starting material, by using an organic acid salt of 4′-epi-daunorubicin or a hydrate or solvate thereof as a novel production intermediate, thus making it possible to produce high-purity epirubicin.
priorityDate 2015-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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