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Eco-Friendly Synthesis and Insecticidal Activity of Some Fluorinated 2-(N-Arylamino)-4-Arylthiazoles

机译:某些氟化2-(N-芳氨基)-4-丙烯腈的生态友好合成及杀虫活性

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A series of fluorinated 2-(N-arylamino)-4-arylthiazoles (3) was synthesized by the condensation of appropriate arylthioureas (2) with corresponding α-bromoacetophenones (1) by using “green chemistry” techniques, viz. mechanochemical mixing and microwave or ultrasonic irradiation. Compared with conventional procedures, the reaction can be carried out under milder conditions, requiring a shorter reaction time and giving higher yields following the green chemistry methodology. All the synthesized compounds were characterized on the basis of elemental analyses and spectral data (IR, 1H NMR, and mass spectrometry). Representative compounds were also evaluated for their insecticidal activity against Helicoverpa armigera, and some of them showed promising activity.Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.View full textDownload full textKeywordsArylthiazoles, arylthioureas, α-bromoacetophenones, eco-friendly synthesis, insecticidal activity, microwave irradiation, sonochemistryRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/10426500903036014
机译:通过使用“绿色化学”技术,通过适当的芳基硫脲(2)与相应的β-溴乙酰苯(1)的缩合,合成了一系列氟化的2-(N-芳基氨基)-4-芳基噻唑(3)。 。机械化学混合以及微波或超声辐射。与常规方法相比,该反应可以在较温和的条件下进行,需要更短的反应时间,并且按照绿色化学方法可以得到更高的产率。根据元素分析和光谱数据(IR, 1 1 H NMR和质谱)对所有合成的化合物进行表征。还评估了代表性化合物对棉铃虫的杀虫活性,其中一些化合物显示出令人鼓舞的活性。本文提供了补充材料。转到出版者的磷,硫和硅以及相关元素的在线版本以查看免费的补充文件。查看全文下载全文关键词阿立噻唑,芳基硫脲,α-溴乙酰苯,环保合成,杀虫活性,微波辐射,声化学相关addthis_config = {ui_cobrand:“泰勒和弗朗西斯在线”,servicescompact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,更多”,发布:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/10426500903036014

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