首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of some new S-triazine based chalcones and their derivatives as potent antimicrobial agents.
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Synthesis of some new S-triazine based chalcones and their derivatives as potent antimicrobial agents.

机译:合成一些新的基于S-三嗪的查耳酮及其衍生物作为有效的抗菌剂。

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摘要

Base catalysed condensation of ketone 5 with different aldehydes give chalcones, 2.4-bis-(phenylamino)-6-[4'-{3''-(4'''-substituted phenyl/2'''-furanyl/2'''-thienyl)-2''-propenon-1''-yl}phenylamino]-s-thriazines 6a-e. These chalcones on cyclization with hydrazine hydrate in the presence of glacial acetic acid, guanidine nitrate in the presence of alkali and malononitrile in the presence of ammonium acetate give the corresponding acetylpyrazolines 7a-e, aminopyrimidines 8a-e and cyanopyridines 9a-e respectively. The products 6a-e, 7a-e, 8a-e and 9a-e were fully characterized by spectroscopic and elemental analysis and also tested for antibacterial activity.
机译:酮5与不同醛的碱催化缩合得到查尔酮,即2.4-双-(苯基氨基)-6- [4'-{3''-(4'''-取代的苯基/ 2'''-呋喃基/ 2'') '-噻吩基)-2'-丙烯-1'-基}苯基氨基] -s-三嗪6a-e。这些查耳酮在冰醋酸存在下用水合肼环化,在碱存在下用硝酸胍在乙酸铵存在下用硝酸胍环化,分别得到相应的乙酰基吡唑啉7a-e,氨基嘧啶8a-e和氰基吡啶9a-e。产品6a-e,7a-e,8a-e和9a-e通过光谱和元素分析得到了充分表征,并且还测试了其抗菌活性。

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