SYNTHESIS OF 3-ARYL[1,2,4]TRIAZOLO[3,4-<i>b</i>][1,3]BENZOTHIAZOLE-6,7-DICARBONITRILES FROM 5-ARYL-4H-TRIAZOLE-2-THIOLS AND 5-BROMO-5-NITROPHTHALONITRILE
DOI:
https://doi.org/10.1007/8381Keywords:
3-aryl[1, 2, 4]triazolo][3, 4-b][1, 3]benzothiazole-6, 7-dicarbonitriles, 4-bromo-5-nitro-phthalonitrile, 4-thiazole-3-thiol, intramolecular nucleophilic substitutionAbstract
New 3-aryl-substituted [1,2,4]triazolo][3,4-b][1,3]benzothiazole-6,7-dicarbonitriles have been synthesized by successive interaction of 5-aryl-4H-triazole-2-thiols with 4-bromo-5-nitrophthalonitrile in the presence of K2CO3 initially at the bromine atoms and then at the nitro group.How to Cite
Abramov, I. G.; Smirnov, A. V.; Kalandadze, L. S.; Gerasimova, N. P.; Nozhnin, N. A.; Sakharov, V. N. Chem. Heterocycl. Compd. 2005, 41, 238. [Khim. Geterotsikl. Soedin. 2005, 270.]
For this article in the English edition, see DOI 10.1007/s10593-005-0134-3