http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S57144261-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D217-04
filingDate 1981-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_991c13adfe04defcd08dd474b2b60841
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bfc698df1193095af28c9bcab644363
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81a397327cbd35786068ca1c8d1e4968
publicationDate 1982-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S57144261-A
titleOfInvention Preparation of n-substituted isoquinolinium salt
abstract PURPOSE: To prepare the titled compound by reacting a tar base mixture containing isoquinoline, quinoline, 2-methylquinoline, etc. with urea, separating 2- methylquinoline as urea adduct, and separating only the titled compound from the residue with a quaternizing agent. n CONSTITUTION: A tar base mixture composed mainly of a fraction having a boiling point of 230W260°C, obtained by distilling a tar base prepared by the acid extraction of coal tar oil or liquefied coal oil, and containing isoquinoline, quinoline, 2-methylquinoline and other alkyl-substituted derivative, is mixed with urea, and 2-methylquinoline is separated as urea adduct. The residual isoquinoline base mixture is mixed with a quatenizing agent of formula R n X (R is organic residue; n is 1 or 2) and made to react at normal temperature W250°C, especially 100W200°C, and the produced N-substituted isoquinolinium salt is separated and purified. n COPYRIGHT: (C)1982,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104788371-A
priorityDate 1981-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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