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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-803
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-80
filingDate 2005-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_246d4be83a9a9bdc3adee1cd347a70ed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99098a10f027ba5a0553b7eec5df852d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41f54cc028588d2a11c600e33cf23091
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a540def311358929c51bbb3032e98f15
publicationDate 2008-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2008262239-A1
titleOfInvention Process for Producing Enantiomer of Amlodipine in High Optical Purity
abstract The present invention relates to a process for preparation of optically pure (S)-amlodipine-L-hemitartrate DMF solvate comprising the steps of treating (R,S) amlodipine base with L-tartaric acid in the presence of dimethyl formamide and a co-solvent. The invention also relates to a process for converting (R) or (S)-amlopidine-L-hemitartrate DMF solvate into their besylates without isolating free chiral amlopidine base after solution.
priorityDate 2004-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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