http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102757414-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-87
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C55-07
filingDate 2011-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca2acd75128ae602d07939106cfcad39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8957739322399659b416620bf8063224
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publicationDate 2014-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102757414-B
titleOfInvention Preparation method of eseitalopram oxalate
abstract The invention provides a preparation method of eseitalopram oxalate. The method comprises the steps that: S)-4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)-phenyl cyanide is dissolved by using an organic solvent; alkali and methylsulfonyl chloride or p-toluene sulfonyl chloride are added for carrying out a reaction; when the reaction is finished, water is added; an organic phase is separated; oxalic acid is directly added into the organic phase, and the mixture is stirred, such that a solution of eseitalopram oxalate is obtained; and a poor solvent is added for crystallization, such that eseitalopram oxalate is obtained. With the method provided by the invention, a defect of easy degradation of product is overcome. The method is advantaged in simple operation, high yield, and high finished product purity. The method is suitable for large-scale industrialized productions.
priorityDate 2011-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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