Synthesis of new 2-substituted 3-(tri(di)fluoromethyl)-quinoxalines from 3-(trifluoromethyl)quinoxalin-2(1H)-one and 3-(tri(di)fluoromethyl)quinoxaline-2-carboxylic acids / Didenko Andrey V.,Vorobiev Mikhail V.,Sevenard Dmitri V.,Sosnovskikh Vyacheslav Ya. // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2015. - V. 51, l. 3. - P. 259-268.

ISSN/EISSN:
0009-3122 / 1573-8353
Type:
Article
Abstract:
{[}GRAPHICS] Starting from 3-(trifluoromethyl)quinoxalin-2(1H)-one, a wide range of new 2-substituted 3-(trifluoromethyl)quinoxalines were obtained, including amino, bromo, chloro, hydrazino, phenyl, alpha-furyl, formyl, methylsulfanyl, and methylsulfonyl derivatives. 3-(Tri(di)-fluoromethyl)quinoxaline-2-carboxylic acids were obtained for the first time and used for the synthesis of 2-amino-3-(tri(di)-fluoromethyl)quinoxalines and 2-(2-aminothiazol-4-yl)-3-(trifluoromethyl)quinoxaline.
Author keywords:
quinoxaline-2-carboxylic acid; quinoxaline-2(1H)-thione; quinoxalin-2(1H)-one; 2-substituted 3-(tri(di)fluoromethyl)-quinoxalines BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY; HETEROCYCLES; TRIFLUOROMETHYLATION; PERFLUOROBIACETYL; RECEPTOR; REAGENT; FACILE
DOI:
10.1007/s10593-015-1694-5
Web of Science ID:
ISI:000354479700009
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 BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY; HETEROCYCLES; TRIFLUOROMETHYLATION; PERFLUOROBIACETYL; RECEPTOR; REAGENT; FACILE
Research-Areas Chemistry
Web-of-Science-Categories Chemistry, Organic
Author-Email sevenard@hfc-chemicals.com vy.sosnovskikh@urfu.ru
Funding-Acknowledgement Federal Ministry of Industry and Technology of Germany {[}EP101205]
Funding-Text This work was performed with financial support from the Federal Ministry of Industry and Technology of Germany (project EP101205). A part of this research was presented at the conference ``Organic synthesis: chemistry and technology{''
Number-of-Cited-References 39
Usage-Count-Last-180-days 3
Usage-Count-Since-2013 10
Journal-ISO Chem. Heterocycl. Compds.
Doc-Delivery-Number CI1CW