Reactions of 1-Alkyl-2-chloro-1H-indole-3-carbaldehyde with 4-Amino-5-alkyl(aryl)-4H-triazole-3-thioles
- Authors: Vikrishchuk N.I.1, Suzdalev K.F.1, Dranikova A.Y.2, Tkachev V.V.3,4, Shilov G.V.3
-
Affiliations:
- Southern Federal University
- Research Institute of Physical and Organic Chemistry
- Institute of Problems of Chemical Physics of the Russian Academy of Sciences
- Institute of Physiologically Active Substances of the Russian Academy of Sciences
- Issue: Vol 89, No 12 (2019)
- Pages: 2369-2373
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223190
- DOI: https://doi.org/10.1134/S1070363219120077
- ID: 223190
Cite item
Abstract
The reaction of 1-alkyl-2-chloro-1H-indole-3-carbaldehydes with 4-amino-5-alkyl(aryl)-4H-1,2,4-triazole-3-thiols afforded new heterocyclic compounds, namely triazolo(thiadiazepino)indoles. Structure of the latter was established by single crystal X-ray diffraction method. This heterocyclic system is formed upon cyclization of the intermediate 5-alkyl-4-[indol-3-yl(methylideneamino)]-4H-1,2,4-triazole-3-thiols.
About the authors
N. I. Vikrishchuk
Southern Federal University
Author for correspondence.
Email: natvi2004@mail.ru
Russian Federation, Rostov-on-Don, 344090
K. F. Suzdalev
Southern Federal University
Email: natvi2004@mail.ru
Russian Federation, Rostov-on-Don, 344090
A. Yu. Dranikova
Research Institute of Physical and Organic Chemistry
Email: natvi2004@mail.ru
Russian Federation, Rostov-on-Don, 344090
V. V. Tkachev
Institute of Problems of Chemical Physics of the Russian Academy of Sciences; Institute of Physiologically Active Substances of the Russian Academy of Sciences
Email: natvi2004@mail.ru
Russian Federation, Chernogolovka, 142432; Chernogolovka, 142432
G. V. Shilov
Institute of Problems of Chemical Physics of the Russian Academy of Sciences
Email: natvi2004@mail.ru
Russian Federation, Chernogolovka, 142432
![](/img/style/loading.gif)