The one pot, three-components condensation of aromatic aldehydes, hydrazine and sulfur in ethanol under microwave irradiation provided symmetrically 3,5-disubstituted 1,3,4-thiadiazoles in high yields and good purity. This reaction must be conducted under pressure of hydrogen sulfide produced in-situ. The structure of the compounds was confirmed by 1H, 13C NMR, MS and elemental analysis.
在微波辐射下,一锅三组分的芳香醛,
肼和
硫在
乙醇中的缩合反应可对称地提供3,5-二取代的1,3,4-
噻二唑,产率高且纯度高。该反应必须在原位产生的
硫化氢的压力下进行。化合物的结构通过1 H,13 C NMR,MS和元素分析确认。