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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Convenient one pot synthesis of some novel derivatives of thiazolo(2,3-b)dihydropyrimidinone possessing 4-methylthiophenyl moiety and evaluation of their antibacterial and antifungal activities.
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Convenient one pot synthesis of some novel derivatives of thiazolo(2,3-b)dihydropyrimidinone possessing 4-methylthiophenyl moiety and evaluation of their antibacterial and antifungal activities.

机译:方便地一锅合成一些具有4-甲硫基苯基的噻唑并(2,3-b)二氢嘧啶酮的新型衍生物,并评估其抗菌和抗真菌活性。

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摘要

A series of new 2-(arylidene/5-arylfurfurylidene)-5-(4-methylthiophenyl)-6-carbethoxy-7-me thyl-5H-thiazolo[2,3-b]pyrimidin-3(1H)-ones 2 and 3 have been synthesized by a three component (MCR) reaction involving 4-(4-methylthiophenyl)-5-carbethoxy-6-methyl-3,4-dihydropyrimidin-2(1H)-th ione 1, monochloroacetic acid and arylaldehydes/arylfurfuraldehydes, respectively. The newly synthesized compounds were well characterized by elemental analysis, IR, (1)H NMR and mass spectral studies. The newly synthesized compounds were screened for their antibacterial and antifungal activities and have exhibited moderate to excellent growth inhibition of bacteria and fungi. The results of such studies have been discussed in this paper.
机译:一系列新的2-(亚芳基/ 5-芳基糠基亚烷基)-5-(4-甲硫基苯基)-6-甲乙氧基-7-甲基5H-噻唑并[2,3-b]嘧啶-3(1H)-ones 2和3是通过三组分(MCR)反应合成的,涉及4-(4-甲基硫代苯基)-5-碳乙氧基-6-甲基-3,4-二氢嘧啶-2(1H)-th离子1,一氯乙酸和芳醛/芳基糠醛分别。通过元素分析,IR,(1)H NMR和质谱研究对新合成的化合物进行了很好的表征。筛选了新合成的化合物的抗菌和抗真菌活性,并显示出对细菌和真菌的中度至极好的生长抑制。此类研究的结果已在本文中进行了讨论。

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