http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2011130587-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B57-00
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filingDate 2009-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e6b1b9a5198b58c6648c87a5a1d86d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff13a2b0ec5ebdcbfdff6d121b90a650
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publicationDate 2011-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2011130587-A1
titleOfInvention Process for preparing r-beta-amino phenylbutyric acid derivatives
abstract Disclosed is a process for preparing single enantiomers of beta-amino phenylbutyric acid derivatives and pharmaceutically acceptable salts thereof, which affords the desired compounds having special optical configuration. The process comprises a step of chemical synthesis and a step of resolving the optical isomers of beta-amino phenylbutyric acid derivatives with a resolving agent. The resolving step comprises reacting the optical isomers with resolving agents, such as di-para-toluoyl-L-tartaric acid and di-para-toluoyl-D-tartaric acid. The obtained R-beta-amino phenylbutyric acid derivatives (I) have high optical purity, and the total yield of the accumulative resolution of the laevo and the dextro isomer is up to above 70%.
priorityDate 2008-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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