Synthesis of N-heteroarylamidines of 1,2,3-thiadiazole-4-carboxylic acid from 2-cyanothioacetamides and 5-azido-1-methyl-4-nitroimidazole / Belyaev Nikolay A.,Beryozkina Tetyana V.,Bakulev Vasiliy A. // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2016. - V. 52, l. 3. - P. 206-208.

ISSN/EISSN:

0009-3122 / 1573-8353

Type:

Article

Abstract:

The reaction of 2-cyanothioacetamides with 5-azido-1-methyl-4-nitroimidazole in ethanol in the presence of sodium ethoxide at 0A degrees D lead to the formation of previously unknown N-heteroarylamidines of 1,2,3-thiadiazole-4-carboxylic acid in 58-76\% yields.

Author keywords:

azides; cyanothioacetamides; imidazoles; 1,2,3-thiadiazoles; thioamides; 1,2,3-triazoles; Cornforth rearrangement REARRANGEMENTS; ATOM

DOI:

10.1007/s10593-016-1861-3

Web of Science ID:

ISI:000376466200015

Соавторы в МНС:

Другие поля

Поле	Значение
Month	MAR
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
EISSN	1573-8353
Keywords-Plus	REARRANGEMENTS; ATOM
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	v.a.bakulev@urfu.ru
Funding-Acknowledgement	Russian Science Foundation {[}15-13-10031]
Funding-Text	This work was performed with financial support from the Russian Science Foundation (grant 15-13-10031).
Number-of-Cited-References	21
Usage-Count-Last-180-days	6
Usage-Count-Since-2013	11
Journal-ISO	Chem. Heterocycl. Compds.
Doc-Delivery-Number	DM6MG