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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-14
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filingDate 1978-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9eb4fe2d7e9927a4695e2152ab04da36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7eb604e951735320bec7a7cbcef8ab39
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publicationDate 1980-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5536403-A
titleOfInvention Preparation of 1-benzazonine derivative
abstract PURPOSE: To obtain the title compound, a lenitive having no side effect, low toxicity and a high biological activity, by making use of the solubility difference of the diastereomeric mixture formed by treatment of a derivative of dl-benzazonine with an optically active organic acid in a solvent. n CONSTITUTION: A derivative of dl-benzazonine of the formula (R=H, methyl) is treated with an optically active organic acid (example; optically active mandelic acid, optically active tartaric acid, etc.) in a solvent to form diastereomeric mixture, form which a derivative of l-benzazonine is isolated by making use of the solubility difference of the isomers to a solvent, e.g. acetone, methyl ethyl ketone, methyl isobutyl ketone, etc. n COPYRIGHT: (C)1980,JPO&Japio
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