4-N,N-Dimethylamino- and 4-cycloamino-5-phenyl-1,2,4-triazole-3-thiones 1–13 have been synthesized from benzhydrazides and substituted methyl dithiocarbazates under various conditions including short microwave irradiations. The last method seemed faster than the classical refluxing one. The influence of base and solvent types on the reaction direction has been also examined. © 2010 Wiley Periodicals
4-N,N-Dimethylamino- 和 4-cycloamino-5-phenyl-1,2,4-triazole-3-thiones 1-13 已经在包括短微波辐射在内的各种条件下由苯甲酰
肼和取代的二
硫代
氨基甲酸甲酯合成。最后一种方法似乎比经典的回流方法更快。还研究了碱和溶剂类型对反应方向的影响。© 2010 Wiley Periodicals, Inc. 杂原子
化学 21:188–195, 2010; 在线发表于 Wiley InterScience (www.interscience.wiley.com)。DOI 10.1002/hc.20594