http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102443000-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_078cb8366425c7f7bb46338421d23406
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-454
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04
filingDate 2010-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2106f6921528ffcfc05274eea1d196e9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2556a037ba93caa0c1ce57b9fa81bc2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fbcc4160dd81edbaed0e7d1775a62814
publicationDate 2014-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102443000-B
titleOfInvention Preparation method of iloperidone
abstract The invention provides a preparation method of iloperidone. The method of the invention comprises reacting 2, 4-difluorophenyl(4-piperidyl) ketoxime and 4-chloropropoxy-3-methoxyacetophenone in an aqueous solution of an alkali metal hydroxide, with the concentration of the alkali metal hydroxide maintained at 20-40%. The method provided in the invention has the advantages of simple process, easy operation, high overall yield, and no generation of compound hard to separate during preparation, and can obtain a qualified finished product through simple recrystallization as well as has no need for purification by column chromatography, thus being suitable for industrial production.
priorityDate 2010-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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