http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1724253-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c999fee6428152a996011d506925c2d7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C227-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-51
filingDate 2006-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_353703dde319f3d5a86d82c2468bfee7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2ca61f3f8b183c80f8a4e765d523f2d
publicationDate 2006-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1724253-A2
titleOfInvention Production method of optically active diphenylalanine compounds
abstract The present invention provides a production method including reacting a diphenylmethylene halide compound represented by the following formula (1) with a malonic acid diester compound represented by the following formula (2) in an organic solvent selected from N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone and N,N-dimethylformamide, in the presence of a base selected from an alkali metal hydride and an alkali metal t-butoxide to give a diester compound represented by the following formula (3), and then subjecting the diester compound to hydrolysis and decarboxylation to give a diphenylalanine compound represented by the following formula (4). n According to the present invention, diphenylalanine compound (4) can be obtained industrially advantageously in a high yield.n nwherein each symbol is as defined in the specification.
priorityDate 2005-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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