EventsThe 21st International Electronic Conference on Synthetic Organic Chemistry
Event submissions
Published
with-doi10.3390/ecsoc-21-04853
This submission belongs to the session A. General Organic Synthesis of the event The 21st International Electronic Conference on Synthetic Organic Chemistry
Published date
07 Nov, 2017
Citation
Victor V. Dotsenko, Darya Yu Lukina, Angela N. Stolyarova, Synthesis of new functionalized thieno[2,3-b]pyridines, in Proceedings of The 21st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2017, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-21-04853
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Synthesis of new functionalized thieno[2,3-b]pyridines

Darya Yu Lukina 1
Angela N. Stolyarova 1
Victor V. Dotsenko 1,2,3
1. Kuban State University, 149 Stavropolskaya Str., Krasnodar 350040, Russian Federation
2. ChemEx Lab, Vladimir Dal’ Lugansk National University, Lugansk, 91034 Russia.
3. North-Caucasus Federal University, 1 Pushkina St., 355009 Stavropol, Russian Federation
Abstract

3-Aminothieno[2,3-b]pyridine-2-carboxamides react with chloroacetyl chloride to afford 3-(chloroacetylamino)thieno[2,3-b]pyridine-2-carboxamides. The latter upon treatment with sodium azide gave 3-(azidoacetylamino)thieno[2,3-b]pyridine-2-carboxamides. The reaction of 3-(chloroacetylamino)thieno[2,3-b]pyridine-2-carboxamides with sulfur and amines afforded new monothiooxamides.

Keywords
thieno[2,3-b]pyridines
acylation
azides
monothiooxamides
Manuscript
ECOSC 21 2017 Stolyarova Lukina azides monothiooxamides.pdf
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