EventsThe 20th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 20th International Electronic Conference on Synthetic Organic Chemistry
Published date
08 Nov, 2016
Citation
Victor V. Dotsenko, Tatyana Yu. Evmeshenko, Gennady D. Krapivin, Synthesis of 6-R-6,7-dihydro-3H,5H-[1,2,4]dithiazolo[4,3-a][1,3,5]triazine-3-thiones by aminomethylation of xanthane hydride, in Proceedings of The 20th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2016, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-20-a064
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Synthesis of 6-R-6,7-dihydro-3H,5H-[1,2,4]dithiazolo[4,3-a][1,3,5]triazine-3-thiones by aminomethylation of xanthane hydride

Tatyana Yu. Evmeshenko 1
Gennady D. Krapivin 4
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
4. Kuban State Technological University, 2 Moskovskaya st., 350072 Krasnodar, Russian Federation
Abstract

Xanthane hydride (5-Amino-3H-1,2,4-dithiazole-3-thione) reacts with primary amines (1 eq.) and HCHO (2 eq.) under harsh conditions (reflux in DMSO) to give a hitherto unknown heterocyclic system, 6,7-dihydro-3H,5H-[1,2,4]dithiazolo[4,3-a][1,3,5]triazine. The products were confirmed by NMR studies.

Keywords
xanthane hydride
Mannich reaction
amnimethylation
NMR studies
dithiazoles
6,7-dihydro-3H,5H-[1,2,4]dithiazolo[4,3-a][1,3,5]triazine
Manuscript
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