SYNTHESIS AND PROPERTIES OF DERIVATIVES OF THE NEW HETEROCYCLIC SYSTEM BENZ[4,5]IMIDAZO[1,2-<i>c</i>]PYRIDO-[3',2';4,5]THIENO[2,3-<i>e</i>]PYRIMIDINE
Keywords:
3-amino-2-(benzimidazolyl)thieno[2,3-b]pyridines, 2-benzimidazolylmethylthio-3-cyanopyridines, benz[4,5]imidazo[1,2-c]pyrido[3',2';4,5]thieno[2,3-e]pyrimidines, 2-chloromethylbenzimidazole, 3-cyanopyridin-2(1H)-thionesAbstract
Derivatives of a new heterocyclic system – benz[4,5]imidazo[1,2-c]pyrido[3',2';4,5]thieno[2,3-e]-pyrimidine have been obtained by successive reactions in three stages – alkylation of 3-cyanopyridine-2(1H)-thiones with 2-chloromethylbenzylimidazole to give 2-benzimidazolylmethylthio-3-cyanopyridines, closing the thiophene ring in the latter to form 3-amino-2-(benzimidazolyl-2)thieno[2,3-b]pyridines, and cyclization of the pyrimidine ring by acylation with carboxylic acid anhydrides or chlorides.
How to Cite
Kambulov, E. Yu.; Vasilin, V. K.; Kaigorodova, E. A.; Konyushkin, L. D.; Krapivin, G. D. Chem. Heterocycl. Compd. 2003, 39, 255. [Khim. Geterotsikl. Soedin. 2003, 287.]
For this article in the English edition, see DOI https://doi.org/10.1023/A:1023736928729