http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-216466-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_334f3ee6eeb9c496c3cce8c9fc4532f0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H5-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H7-06
filingDate 1983-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c65bf6d8bf0ba9e580066b8f3fb963a7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee457bb7f8a370123d07260bd0630e6e
publicationDate 1984-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-216466-A1
titleOfInvention PROCESS FOR THE PREPARATION OF GLUCOPYRANOSYLTHIONICOTINONITRILENE
abstract The invention relates to a process for the preparation of substituted glucopyranosylthionicotinonitriles. The aim of the invention is to develop a process for the preparation of 2- (2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosylthio) -4-aryl-6-bromo-nicotinonitriles. The substituted Glucopyranosylthioicotinonitrile of the general formula II, in which R is an optionally halogen-, alkyl- or alkoxy-substituted phenyl radical, can be prepared by reacting the methylsulfonylnicotinonitriles of the general formula I in which R has the above meaning, with the 2,3,4, 6-Tetra-O-acetyl-beta-D-glucopyranosyl mercaptan. These substituted glucopyranosylthionicotinonitriles can be used as organic intermediates for further syntheses. They are particularly suitable for the preparation of other derivatives of Nicotinonitrile.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-19542550-C2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5399488-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-19542550-A1
priorityDate 1983-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 24.