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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
filingDate 2014-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c29ea156cfb9a0340212bb3fdcd97424
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_61f4d6001bb9010d85f25aa2ecaa859e
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publicationDate 2014-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8853395-B2
titleOfInvention Process for the preparation of lurasidone hydrochloride
abstract Disclosed is a new and efficient process for the synthesis with high yields and purity of lurasidone hydrochloride, a medicament which is useful as a psychotropic substance. The process involves the preparation of lurasidone base in a reaction system not containing inorganic salts, followed by conversion of the latter to an addition salt with an organic carboxylic acid, which is finally converted to lurasidone hydrochloride.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10426770-B2
priorityDate 2013-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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