http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54115373-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f6e33603375c486b0ab3505830af9e8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-32
filingDate 1978-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78b587d36e90f4d8b537fc507917cfb0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a30627813d5aa5ff84acd7ad8e1b816
publicationDate 1979-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S54115373-A
titleOfInvention Preparation of heterocyclic compound
abstract PURPOSE: To obtain the title compound useful as aralgesics and intermediates for medicines in a very short step in high yield, by treating a pypridinium salt with a base to give a specific compound, which is hydrolyzed under acidic conditions. n CONSTITUTION: A pyridinium salt of formula I: [R 1 is lower alkyl or aralkyl group; R 2 ' is H when X' is 0, R 2 ' is lower alkyl or aryl group when Z' is imino group; R 3 is H or lower alkyl group; -W=Y-Z' is formula II (R 4 is H, lower alkenyl group. etc.) etc.; X is halogen] is treated with a base, e.g. sodium hydroxide or sodium carbonate, to give a compound of formula III: (A is R 1 -N=CH; R 2 is present when Z is N, and the same as R 2 '; -W=Y-Z is formula IV, etc.), which is hydrolyzed under acidic conditions with hydrochloric acid to form the compound of formula V: (B is R 1 -N=CH, etc.). n COPYRIGHT: (C)1979,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002069061-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104262270-A
priorityDate 1978-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 25.