http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0135351-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5610690048edbc271e03b26b23f76ff9
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C271-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C271-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C239-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
filingDate 1984-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6b28dbc18a114739333172a9ac9b994
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3efaac12262c1b95a3f0b1459d4b6211
publicationDate 1985-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0135351-A1
titleOfInvention Manufacturing process for N-carbobenzyloxy-L-glutamic acid-alpha-cholinester salt
abstract The invention relates to manufacturing process for a halide or an organic sulfonate of N-carbobenzyl-L-glutamic acid-a-cholinester in high purification, which is useful as e.g. hypotensive drug. According to the prior art, undesired γ-form byproduct is inevitably formed to be mingled with said a-form objective compound of which separation is difficult. It has been found that when using N-carbobenzyloxy-γ-tert. butyl-L-glutamic acid-dicyclohexyl-ammonium salt readily available in high purification as starting material, reacting N, N-dimethyl-aminoethylchloride therewith to form N-carbobenzyloxy-γ-tert. butyl-L-glutamic acid-a-dimethylaminoethyl ester which is quarternerized to form N-carbobenzyloxy-γ-tert. butyl-L-glutamic acid- α-cholinester salt, which is subjected to mild salt treatment, the objective compound can be obtained in high purification.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-567014-B1
priorityDate 1983-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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