http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014031372-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-46
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-403
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10
filingDate 2013-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_223a175b01bc18b9559f20f9f820f8ef
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb0a3f673e7c4188325282f1d28ef8ec
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publicationDate 2014-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2014031372-A
titleOfInvention An efficient method for preparing high purity mitiglinide
abstract The present invention provides an efficient method for preparing high purity mitiglinide. A) converting (S) -2-benzylsuccinic acid XII to the corresponding acid chloride; b) esterifying XV to diester XVI using N-hydroxysuccinimide. c) regioselective reaction of diester XVI with cis-hexahydroisoindoline to give monoamide monoester XVII; d) hydrolysis of the ester group of XVII to give mitiglinide (I); and Accordingly, e) preparation by a step of chlorinating mitiglinide to the corresponding calcium salt dihydrate (II). [Selection figure] None
priorityDate 2012-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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