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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C313-00
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filingDate 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1bd4b935c334f8bca5dfe86165c1842
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c3fc14e47796b42741a1e2ffb801ad9
publicationDate 1988-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S63218655-A
titleOfInvention Optical resolution of n-carbamoylmethionine
abstract PURPOSE: To form two kinds of diastereomeric salts and optically resolve the resultant salts, by reacting (±)-N-carbamoylmethionine with optically active α-ethylbenzylamine or 2-amino-1-butanol as a resolving agent. n CONSTITUTION: Optically active α-ethylbenzylamine (abbreviated to EBA) or 2-amino-1-butanol (abbreviated to 2AB) and a solvent, such as water r alcohols, are added to (±)-N-carbamoylmethionine [abbreviated to (±)-NCM] and dissolved at 50°C W boiling temperature while heating to provide supersaturation. The resultant mixture is then cooled to room temperature and the formed diastereomeric salts are resolved. The optically active EBA or 2AB is used in a molar amount of 0.3W1.5 times based on the (±)-NCM. The methionine is one of essential amino acids and useful as a medicine, such as formula feed for domestic animals, food and amino acid transfusion solution. n COPYRIGHT: (C)1988,JPO&Japio
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priorityDate 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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