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Synthesis of pyrazolines,isoxazolines and aminopyrimidines as biological potent agents

机译:吡唑啉,异恶唑啉和氨基嘧啶类生物强剂的合成

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摘要

Chalcones,2-phenylamino-4-(4'-fluorophenylamino)-6-[4'-{3"-(phenyl/substituted phenyl /2"'-furanyl/3'"-pyridinyl)-2"-propenon-l"-yl} phenylamino]-s-triazines 6a-j have been prepared from ketone 5 based on s-triazine nucleus.These chalcones 6a-j on cyclisation with hydrazine hydrate,hydroxylamine hydrochloride and guanidine nitrate give the corresponding pyrazolines 7a-j,isoxazolines 8a-j and aminopyrimidines 9a-j,respectively.Antimicrobial activities of all synthesized compounds have been performed by using cup-plate method against bacteria and by using poisoned food technique against fungi.The constitutions of newly synthesized compounds have been established on the basis of elemental analysis,IR and ~1H NMR spectral data.
机译:Chalcones,2-phenylamino-4-(4'-fluorophenylamino)-6- [4'-{3“-(苯基/取代的苯基/ 2”'-呋喃基/ 3'“-吡啶基)-2”-丙烯-1由基于s-三嗪核的酮5制备了“ -yl}苯基氨基] -s-三嗪6a-j。这些查耳酮6a-j在与水合肼,盐酸羟胺和硝酸胍环合后得到相应的吡唑啉7a-j,分别通过异物杯法和细菌中毒食品技术对所有合成的化合物进行了抗菌活性研究,并在此基础上建立了新合成化合物的结构元素分析,IR和〜1H NMR光谱数据。

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