首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Novel 2,4,5-trisubstituted oxazole derivatives: synthesis and antiproliferative activity.
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Novel 2,4,5-trisubstituted oxazole derivatives: synthesis and antiproliferative activity.

机译:新型2,4,5-三取代的恶唑衍生物:合成和抗增殖活性。

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摘要

Microwave irradiation promotes the rapid O,N-acylation-cyclodehydration cascade reaction of oximes and acid chloride. Twenty novel 2,4,5-trisubstituted oxazole derivatives containing heterocycle moiety were synthesized and evaluated for their antiproliferative activity. The twenty compounds are all first reported and their structures were established by elemental analysis, (1)H NMR and (13)C NMR spectra. The bioassay tests showed that compounds 2-(2-(2-fluorophenyl)-4-(2,3,4-trimethoxyphenyl)oxazol-5-ylthio)benzo[d]thiazole (6af), 2-(2-(pyridin-3-yl)-4-(2,3,4-trimethoxyphenyl)oxazol-5-ylthio)pyrimidine (6bg) and 2-(2-(2-fluorophenyl)-4-(2,3,4-trimethoxyphenyl)oxazol-5-ylthio)-5-methyl-1,3,4-t hiadiazole (6cf) displayed good antiproliferative activity in vitro, which were comparable to the positive control (5-fluorouracil).
机译:微波辐射促进了肟和酰氯的快速O,N-酰化-环脱水级联反应。合成了二十种含有杂环部分的新型2,4,5-三取代的恶唑衍生物,并对其抗增殖活性进行了评估。首次报道了这20种化合物,并通过元素分析,(1)H NMR和(13)C NMR光谱确定了它们的结构。生物测定测试表明,化合物2-(2-(2-氟苯基)-4-(2,3,4-三甲氧基苯基)恶唑-5-基硫基)苯并[d]噻唑(6af),2-(2-(吡啶) -3-基)-4-(2,3,4-三甲氧基苯基)恶唑-5-基硫基)嘧啶(6bg)和2-(2-(2-氟苯基)-4-(2,3,4-三甲氧基苯基)恶唑-5-基硫基)-5-甲基-1,3,4-叔二唑(6cf)在体外显示出良好的抗增殖活性,与阳性对照(5-氟尿嘧啶)相当。

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