2-((3-氰-4,6-二酰基吡啶-2-基)硫代乙酰胺及其环化形式的合成及生物活性

S. A. Abdel-Raheem
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引用次数: 19

摘要

本文制备了2-((3-氰-4,6-二苯基吡啶-2-酰基)硫代)乙酰胺(2)及其环化形式3-氨基-4,6-二苯基噻吩[2,3-b]吡啶-2-羧酰胺(3),并通过元素分析和光谱分析对其结构进行了表征。以啶虫脒为对照,研究了它们对豇豆蚜虫的生物活性。化合物(2)和(3)对豇豆蚜虫若虫的生物活性测定结果表明,处理24 h的LC50分别为0.192和0.841 ppm,处理48 h的LC50分别为0.041和0.095 ppm。另外,化合物(2)和(3)对豇豆蚜成虫处理24 h后的LC50分别为1.233和2.949 ppm,处理48 h后的LC50分别为0.142和0.270 ppm。鉴于这些观察结果,已经发现在生物活性和所用化合物的结构之间存在着显著的关系。
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Synthesis and biological activity of 2-((3-Cyano-4,6-distyrylpyridin-2-yl) thio) acetamide and its cyclized form
In this paper, 2-((3-Cyano-4,6-distyrylpyridin-2-yl)thio)acetamide (2) and its cyclized form, 3-amino-4,6-distyrylthieno[2,3-b]pyridine-2-carboxamide (3), were prepared and their structure characterizations were performed by the means of elemental and spectroscopic analyses. Their biological activity as insecticides against cowpea aphid Aphis craccivora Koch using acetamiprid insecticide as a reference was studied. The bioassay results for compounds (2) and (3) against nymphs of cowpea aphid showed that the LC50 values were 0.192 and 0.841 ppm, respectively, after 24 h of treatment but the LC50 values were 0.041 and 0.095 ppm, respectively, after 48 h of treatment. Furthermore, the bioassay results for compounds (2) and (3) showed that the LC50 values were 1.233 and 2.949 ppm, respectively, after 24 h of treatment and the LC50 values were 0.142 and 0.270 ppm, respectively, after 48 h of treatment against adults of cowpea aphid. Given these observations, it has been found that there is a remarkable relationship between the biological activity and the structure of the used compounds.
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