Synthesis 5-(pyrazolin-3-ylmethylidene)-2-thiohydantoins and 2-alkylsulfanyl-5-(pyrazolin-3-ylmethylidene)-3,5-dihydro-4H-imidazol-4-ones
作者:N. I. Vorozhtsov、L. A. Sviridova、O. S. Grigorkevich、D. D. Korablina、E. K. Beloglazkina、A. G. Majouga、N. V. Zyk
DOI:10.1007/s11172-017-1764-1
日期:2017.3
A reaction of 3-allyl- and 3-phenylthiohydantoins with 1,5-diphenyl- and 1-phenyl-substituted 3-formyl-2-pyrazolines was used to obtain a series of 5-(pyrazolin-3-ylmethylidene)-2-thioxotetrahydro-4H-imidazol-4-ones, the subsequent alkylation of which with methyl iodide or ethyl chloroacetate gave the corresponding 2-alkylthio-5-(pyrazolin-3-ylmethylidene)-3,5-dihydro-4H-imidazol-4-ones in the yields
3-烯丙基-和3-苯基硫代乙内酰脲与1,5-二苯基-和1-苯基-取代的3-甲酰基-2-吡唑啉反应得到一系列5-(吡唑啉-3-基亚甲基)-2- thioxotetrahydro-4H-imidazol-4-ones,随后用碘甲烷或氯乙酸乙酯对其进行烷基化,得到相应的 2-烷硫基-5-(pyrazolin-3-ylmethylidene)-3,5-dihydro-4H-imidazol-4-产率从 30% 到 77% 不等。(5Z)-3-苯基-5-[(1,5-diphenylpyrazolin-3-yl)methylidene]-2-methylsulfanyl-4,5-dihydroimidazol-4-one 与四乙酸铅氧化得到相应的吡唑48% 的收率。