Reaction of 2-Aryl-4-Cyano-1,3-Oxazole-5-Sulfonyl Chlorides With 5-Amino-1H-Pyrazoles and 5-Amino-1H-1,2,4-Triazole View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-03-22

AUTHORS

A. N. Kornienko, S. G. Pil’o, A. P. Kozachenko, V. M. Prokopenko, E. B. Rusanov, V. S. Brovarets

ABSTRACT

The reaction of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides with 5-amino-3-R-1H-pyrazoles and 5-amino-1H-1,2,4-triazole gave 5-[(3-R-5-amino-1H-pyrazol-1-yl)sulfonyl]-2-aryl-1,3-oxazole-4-carbo- nitriles and 5-[(5-amino-1H-1,2,4-triazol-1-yl)sulfonyl]-2-aryl-1,3-oxazole-4-carbonitriles. The action of sodium hydride on these carbonitriles leads to the elimination of sulfur dioxide and cyclocondensation to give new heterocyclic systems, namely, [1,3]oxazolo[5,4-d]pyrazolo[1,5-a]-pyrimidine and [1,3]oxazolo[5,4-d][1,2,4]triazolo[1,5-a]pyrimidine.

PAGES

76-86

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-014-1450-2

DOI

http://dx.doi.org/10.1007/s10593-014-1450-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1024048135


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