4,6-DIMETHYLPYRIDINE-2,3-DICARBONITRILE AND ITS REACTION WITH <i>N</i>-ACYLHYDRAZINES
DOI:
https://doi.org/10.1007/1412Keywords:
N'-(7-amino-2, 4-dimethyl-5H-pyrrolo[3, 4-b]pyridin-5-ylidene)carbohydrazides, N'-(5-amino-2, 4-dimethyl-7H-pyrrolo[3, 4-b]pyridin-7-ylidene)carbohydrazides, N-acylhydrazones, 4, 6-dimethylpyridine-2, 3-dicarbonitrile, N', N"-(2, 4-b]pyridine-5, 7-diylidene)dicarbohydrazides, nucleophilic substitution of hydrogen, cyanationAbstract
An efficient method has been developed for the synthesis of 4,6-dimethylpyridine-2,3-dicarbonitrile. A study was carried out on the reaction of this compound with N-acylhydrazines to give two structural isomers, namely, N'-(7-amino-2,4-dimethyl-5H-pyrrolo[3,4-b]pyridin-5-ylidene)carbohydrazides and N'-(5-amino-2,4-dimethyl-7H-pyrrolo[3,4-b]pyridin-7-ylidene)carbohydrazides as well as disubstituted N',N"-(2,4-dimethyl-5H-pyrrolo[3,4-b]pyridine-5,7-diylidene)dicarbohydrazides.
Authors: I. V. Rudenko, A. A. Kucherak, A. A. Tolmachev, and O. V. Hordiyenko.
English translation in Chemistry of Heterocyclic Compounds, 2011, 47 (8), pp 964-969