Heterocyclization of 1-aryl/alkyl-2-thiobiureas to 4-aryl/alkyl-3-substituted-Δ 2 -1,2,4-triazolin-5-ones
作者:M.M Suni、Vipin A Nair、C.P Joshua
DOI:10.1016/s0040-4020(01)00018-7
日期:2001.3
Synthesis of a range of 1,2,4-triazolin-5-ones has been carried out by thermally induced cyclization of 1-aryl/alkyl-2-alkyl isothiobiureas 4. The required isothiobiureas were generated in situ by the reaction of alkyl halides with 1-aryl/alkyl-2-thiobiureas 3 in acidic medium at reflux. The reaction proceeds after S-alkylation of the thiobiureas and is demonstrated by the isolation of the alkyl isothiobiurea intermediates and their subsequent acid catalyzed thermal cyclization. (C) 2001 Elsevier Science Ltd. All rights reserved.
276. The reactions of thiocarbonyl chloride. Part V. With compounds containing the –NH·NH<sub>2</sub>group
作者:Thomas Beckett、G. Malcolm Dyson
DOI:10.1039/jr9370001358
日期:——
Guha; Chakraborty, Journal of the Indian Chemical Society, 1929, vol. 6, p. 106