http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005281207-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
filingDate 2004-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_662443c00b38800aa450c43a0ba20706
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_949a049bd0769af176653115a2a502dd
publicationDate 2005-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2005281207-A
titleOfInvention Method for producing iopamidol
abstract Provided is a method for shortening the reaction time without increasing the generation of impurities when synthesizing iopamidol by deacetylation of a precursor compound. The precursor N, N′-bis [2-hydroxy-1- (hydroxymethyl) ethyl] -5-[(2S) -2-acetoxypropanoylamino] -2,4,6-tri When iopamidol is produced by deacetylation of iodophthalamide, the deacetylation reaction is carried out in an alkaline atmosphere as a solution of alcohols. [Selection figure] None.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012509290-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105272899-A
priorityDate 2004-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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