SYNTHESIS, REACTIONS AND BIOLOGICAL ACTIVITY OF 2-SUBSTITUTED 3-CYANO-4,6-DIMETHYLPYRIDINE DERIVATIVES
DOI:
https://doi.org/10.1007/6876Ключевые слова:
isoxazolopyridine, pyrazolopyridine, pyridine-3-carbonitrile, pyridoquinazoline, antibacterial activityАннотация
The reaction of 2-chloro-4,6-dimethylpyridine-3-carbonitrile with hydrazine hydrate, hydroxylamine, and anthranilic acid afforded the corresponding pyrazolo, isoxazolo, and pyridoquinazoline derivatives. Alkylation of 2-mercapto-4,6-dimethyl-
pyridine-3-carbonitrile with ethyl chloroacetate or phenacyl bromide followed by cyclization in NaOH gave thienopyridine derivatives. Diazotization of ethyl 3-amino-4,6-dimethylthiеno[2,3-b]pyridine-2-carboxylate followed by the reaction with thiourea, guanidine carbonate, and hydroxylamine hydrochloride gave the corresponding thienopyridine derivatives. The biological activity of some new compounds has been discussed.
How to Cite
Yassin, F. A. Chem. Heterocycl. Compd. 2009, 45, 35. [Khim. Geterotsikl. Soedin. 2009, 43.]
For this article in the English edition see DOI https://doi.org/10.1007/s10593-009-0222-x
