5-amino-3,4-dihydro-2h-1,2,4-triazole-3-thiones. synthesis and chemosensor properties View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-09

AUTHORS

I. E. Tolpygin, E. N. Shepelenko, G. S. Borodkin, A. D. Dubonosov, V. A. Bren’, V. I. Minkin

ABSTRACT

The reaction of 4-arylalkyl- and 4-arylthiosemicarbazides with aroyl isothiocyanates gave substituted 1,2-bis(thiocarbamoyl)hydrazines, which readily cyclize to give previously unreported 4-aroyl 5-arylalkyl- and 4-aroyl-5-arylamino-2H-1,2,4-triazole-3-thiones, respectively. A spectral study of 9-anthrylmethylthiosemicarbazides and derived dihydrotriazolethione indicated the chemosensor activity of these compounds relative to a cation series.

PAGES

542-546

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-010-0543-9

DOI

http://dx.doi.org/10.1007/s10593-010-0543-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1047373536


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