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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C313-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
filingDate 1982-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0943b5a3ba824e636e53006b2ea7cafc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8665f1f65ac63ac79281981f202c9068
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publicationDate 1984-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5925370-A
titleOfInvention Preparation of pantethine
abstract PURPOSE: To obtain industrially and advantageously the titled compound useful as a medicine, by reacting a salt of pantothenic acid with cystamine or a salt thereof in the presence of a tertiary alkylamine and an inexpensive condensing agent. n CONSTITUTION: A salt of pantothenic acid is reacted with cystamine or a salt thereof in the presence of a tertiary alkylamine and a condensing agent of suflonyl chloride or an acyl halide in a solvent, e.g. pyridine, at 0W50°C for 30minW several hr to give the amined compound. n EFFECT: The aimed compound can be produced in high yield in a very short time without using a promoter, and the resultant aimed substance can be easily isolated by the convertional method. n COPYRIGHT: (C)1984,JPO&Japio
priorityDate 1982-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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