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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-135
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-22
filingDate 2008-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9050f96942716a48c423f6dfeaccabc4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a38e5b0846f554ed46f5e1d239fcb33e
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publicationDate 2012-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8101769-B2
titleOfInvention Process for preparing ethyl (S)-2-ethoxy-4-[N-[1-(2-piperidinophenyl)-3-methyl-1-butyl]aminocarbonyl methyl]benzoate and use thereof for the preparation of Repaglinide
abstract Described herein is an improved, commercially viable and industrially advantageous process for the preparation of Repaglinide intermediate, ethyl (S)-2-ethoxy-4-[N-(1-(2-piperidino-phenyl)-3-methyl-1-butyl)-aminocarbonylmethyl]-benzoate. The process provides the Repaglinide intermediate in higher yield and purity compared to the previously disclosed processes, thereby providing for production of Repaglinide and its pharmaceutically acceptable salts in high purity and in high yield.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2012065404-A1
priorityDate 2007-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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