http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2105063-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B27-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-82
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B27-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B43-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-82
filingDate 1971-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1972-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2105063-A1
titleOfInvention Sulphonylamidrazone prepn - single stage process using oxidation agents
abstract Sulphonylamidrazones are prepd. by reaction of amidrazones in a single stage with sulphinic acids in the presence of oxidation agents e.g. K persulphate, K hexacyanoferrate (111), KMnO4 or K bichromate. The prodts. are of formula: (where R1 = aryl; R2 = alkyl; R3 = alkyl; R4 = alkyl or aryl; or R1 and R2 together represent a gp. necessary for completion of a 5 or 6-membered hetero ring or R2 and R3 together represent a gp. necessary for completion of a 5-, 6- or 7-membered hetero ring). The prodts. are intermediates in the synthesis of azo dyes - can be used in colour photography.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0967211-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6124242-A
priorityDate 1971-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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