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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
filingDate 2008-01-08^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c9c56b31388a7ed336f4961feb2818e
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publicationDate 2008-07-24^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2008087557-A2
titleOfInvention An improved process for preparation of 9-hydroxy-3-(2-chloroethyl)- 2-methyl-4h-pyrido[1,2-a]pyrimidin-4-one hydrochloride
abstract Described herein is an improved, commercially viable and industrially advantageous process for the preparation of paliperidone intermediate 9-hydroxy-3-(2-chloroethyl)-2- methyl-4h-pyrido[1,2-a]pyrimidin-4-one and its hydrochloride salt. The process provides the paliperidone intermediate in higher yield and reduced reaction time compared to the previously disclosed processes, thereby providing for production of paliperidone and its pharmaceutically acceptable acid addition salts in high purity and in high yield.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011030224-A3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7820816-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2202234-A1
priorityDate 2007-01-08^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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