http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106083748-A

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filingDate 2016-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da0f70ffa9e854d77c7a16eb69f100be
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publicationDate 2016-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106083748-A
titleOfInvention A kind of preparation method of Anastrozole
abstract The invention provides a kind of preparation method of anastrozole, comprises the following steps: 1) with 5-bromomethyl-α, α, α', α'-tetramethyl-1, 3-benzenediacetonitrile and 4- Amino-1,2,4-triazole is used as a raw material, reacted in an organic solvent, and crystallized to obtain intermediate I, namely α, α, α′, α′-tetramethyl-5-[(4-amino -1,2,4-triazolyl)-methylene]-1,3-benzenediacetonitrile bromide salt; 2) intermediate I was dissolved in a solvent, added a small amount of water, acid and metal catalyst, under reflux Add sodium azide in batches, after the reaction is complete, filter while it is hot, concentrate the mother liquor to 0.25-0.75 times the original volume, cool and crystallize, filter the solid, extract it with base adjustment, and concentrate to obtain the crude product of anastrozole; 3) the anastrozole The crude product was dissolved in alcohol solvent, decolorized, cooled and crystallized to obtain the fine product of Anastrozole. The present invention avoids the generation of isanastrozole impurity that affects the drug efficacy from the source, and the isanastrozole is not detected, and the other simple impurities are less than 0.05%, and the total impurities are less than 0.2%.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110028458-B
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109096146-A
priorityDate 2016-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2172449-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007054963-A2
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Total number of triples: 30.