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首页> 外文期刊>Archiv der Pharmazie >Convenient synthesis and antimicrobial activity of new 3-substituted 5-(benzofuran-2-yl)-pyrazole derivatives.
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Convenient synthesis and antimicrobial activity of new 3-substituted 5-(benzofuran-2-yl)-pyrazole derivatives.

机译:新型3取代的5-(苯并呋喃-2-基)-吡唑衍生物的便捷合成和抗菌活性。

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摘要

The reaction of ethyl 4-(benzofuran-2-yl)-2,4-dioxobutanoate 2 with two moles of hydrazine hydrate afforded 5-(benzofuran-2-yl)-1H-pyrazole-3-carbohydrazide 4a, while its reaction with equimolar amount of phenylhydrazine gave ester 3b which then converted to 5-(benzofuran-2-yl)-1-phenyl-1H-pyrazole-3-carbohydrazide 4b. Various new compounds such as imides 5 and 6, acyl hydrazones 7 and 8, bi-pyrazoles 9-12, and 1,3-thiazole derivatives 14 and 15 were prepared from carbohydrazide derivatives 4a, b. The new compounds are tested for their antimicrobial activity. Compounds 2, 5, 7, and 8 showed antifungal activities against C. albicans. Also, compounds 2, 6, 8, and 15 showed antibacterial activities.
机译:4-(苯并呋喃-2-基)-2,4-二氧代丁酸乙酯2与两摩尔水合肼的反应制得5-(苯并呋喃-2-基)-1H-吡唑-3-碳酰肼4a,同时与等摩尔量的苯肼得到酯3b,然后将其转化为5-(苯并呋喃-2-基)-1-苯基-1H-吡唑-3-碳酰肼4b。由碳酰肼衍生物4a,b制备了各种新化合物,例如酰亚胺5和6,酰基hydr7和8,联吡唑9-12和1,3-噻唑衍生物14和15。测试了新化合物的抗菌活性。化合物2、5、7和8对白念珠菌具有抗真菌活性。同样,化合物2、6、8和15显示出抗菌活性。

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