PHENYLFURYLTHIENO[2,3-<i>b</i>]PYRIDYLMETHANES. SYNTHESIS AND REACTIONS OF THE FURAN RING TRANSFORMATION

Authors

  • Д. Ю. Косулина Kuban State University of Technology, Krasnodar 350072
  • В. К. Василин Kuban State University of Technology, Krasnodar 350072
  • Т. А. Строганова Kuban State University of Technology, Krasnodar 350072
  • Е. А. Сбитнева Kuban State University of Technology, Krasnodar 350072
  • А. В. Бутин Kuban State University of Technology, Krasnodar 350072
  • Г. Д. Крапивин Kuban State University of Technology, Krasnodar 350072

DOI:

https://doi.org/10.1007/6588

Keywords:

3-amino-2-benzoylthieno[2, 3-b]pyridines, N-[2-(2, 5-dioxo-1-phenylhexyl)thieno[2, 3-b]pyrid-3-yl]benzamides, (phenyl)(2-acylaminothieno[2, 3-b]pyrid-2-yl)carbinols, (phenyl)(5-methylfur-2-yl)-(2-acylaminothieno[2, 3-b]pyrid-2-yl)methanes, 4-(3-phenyl-1H-pyrrolo[2', 3', 4, 5]thieno[2, 3-b]pyrid-2-yl)-butan-2-ones, alkylation, acylation, reduction, transformation of the furan ring

Abstract

Triarylmethane derivatives with various  substituents, phenyl, 5-methyl-2-furyl, and 3-acylamino-thieno[2,3-b]pyrid-2-yl have been obtained for the first time. The behavior  of  these  compounds  under protolytic conditions has been studied. It was  shown  that the character of the protection of the amino group of the thienopyridine fragment affects the type of transformation of the furan ring.

How to Cite
Kosulina, D. Yu.; Vasilin, V. K.; Stroganova, T. A.; Sbitneva, E. A.; Butin, A. V.; Krapivin, G. D.  Chem. Heterocycl. Compd. 2009, 45, 1105. [Khim. Geterotsikl. Soedin. 2009, 1380.]

For this article in the English edition see DOI 10.1007/s10593-009-0401-9


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Published

2022-02-14

Issue

No. 9 (2009)

Section

Original Papers