Reduction of 1-alkyl/aryl-3-(4-alkyl-5-alkylimino-Δ2-1,2,4-thiadiazolin-3-yl) thioureas: Formation of 1,3,5-triazine-2-thiones
Corresponding Author(s) : Sheena V. Nair
sheenanair2000@yahoo.com
Asian Journal of Chemistry,
Vol. 16 No. 2 (2004): Vol 16 Issue 2
Abstract
Reduction of 1-alkyl/aryl-3-(4-alkyl-5-alkylimino-Δ2-1,2,4-thiadiazolin-3-yl) thioureas in a basic medium yields 1,3-diakyl-4-alkyl/arylimino-6-iminohexahydro-1,3,5,-triazine-2-thiones. The structure assigned to these triazines was based on the substituent pattern on the chain formed by the ring opening and its reaction towards alkali.
Keywords
Synthesis
Thioureas
Triazines
R. Surve, S., & V. Nair, S. (2016). Reduction of 1-alkyl/aryl-3-(4-alkyl-5-alkylimino-Δ2-1,2,4-thiadiazolin-3-yl) thioureas: Formation of 1,3,5-triazine-2-thiones. Asian Journal of Chemistry, 16(2), 800–804. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/14581
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