Reaction of 1-Aryl-3-methylpyrazol-5-ones with 2-Cyanoaryldiazonium Bisulfates View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2005-02

AUTHORS

M.-G. A. Shvekhgeimer, O. A. Ushakova, V. V. Nesterov, M. Yu. Antipin

ABSTRACT

2-Cyanoaryldiazonium bisulfates, obtained by the action of nitrosyl sulfuric acid on isatin 3-hydrazone and its 5-bromo and 5-nitro derivatives, couple with 1-aryl-3-methylpyrazol-5-ones and form 4-arylhydrazones of 1-aryl-3-methylpyrazole-4,5-diones. It was established on the basis of data of IR, UV, and 1H NMR spectra and of X-ray structural analysis that the coupling products exist in the hydrazone form stabilized by an intramolecular hydrogen bond. More... »

PAGES

181-186

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-005-0124-5

DOI

http://dx.doi.org/10.1007/s10593-005-0124-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1016960494


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