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首页> 外文期刊>Journal of Young Pharmacists >Synthesis and Antimicrobial Activity of 2-[2-(2,6-dichloro phenyl) amino]benzyl-3-(5-substituted phenyl-4,5-dihydro-1H-pyrazol-3-ylamino)- 6,8-dibromoquinazolin-4(3H)ones
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Synthesis and Antimicrobial Activity of 2-[2-(2,6-dichloro phenyl) amino]benzyl-3-(5-substituted phenyl-4,5-dihydro-1H-pyrazol-3-ylamino)- 6,8-dibromoquinazolin-4(3H)ones

机译:2- [2-(2,6-二氯苯基)氨基]苄基-3-(5-取代的苯基-4,5-二氢-1H-吡唑-3-基氨基)-6,8-二溴喹唑啉的合成及抗菌活性-4(3H)个

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`A series of 2-[2-(2,6-dichlorophenyl)amino]benzyl-3-(5-substituted phenyl-4,5-dihydro-1H-pyrazol-3-yl-amino)- 6,8-dibromoquinazolin-4(3H) ones 6a-m have been synthesized by the reaction of 2-[2-(2,6-dichlorophenyl) amino]benzyl-3-substituted phenylacrylamido-6,8-dibromoquinazolin-4(3H) ones 5a-m with hydrazine hydrate in the presence of glacial acetic acid. The chalcones 5a-m were prepared by the condensation of 2-[2-(2,6-dichlorophenyl)amino]benzyl-3-acetamido-6,8-dibromoquinazolin-4(3H)one 4 with different substituted aromatic aldehyde. The benzoxazinone 2 was synthesized from 2-[2-(2,6-dichlorophenyl)amino]phenyl acetyl chloride 1 on treatment with 3,5-dibromoanthranilic acid in pyridine, which on reaction with hydrazine hydrate and then on acetylation reaction yielded 4. The structures of these compounds have been elucidated by elemental analyses, IR, and NMR spectral data. The title compounds pyrazolyl-quinazolin-4(3H)ones 6a-m were evaluated for their antibacterial and antifungal activities in vitro.
机译:`一系列2- [2-(2-(2,6-二氯苯基)氨基]苄基-3-(5-取代的苯基-4,5-二氢-1H-吡唑-3-基-氨基)-6,8-二溴喹唑啉通过2- [2-(2-(2,6-二氯苯基)氨基]苄基-3-取代的苯基丙烯酰胺基-6,8-二溴喹唑啉-4(3H)的反应合成了-4(3H)6a-m。在冰醋酸存在下与水合肼反应。通过将2- [2-(2,6-二氯苯基)氨基]苄基-3-乙酰氨基-6,8-二溴喹唑啉-4(3H)one 4与不同的取代的芳族醛缩合来制备查耳酮5a-m。苯并恶嗪酮2是由2- [2-(2,6-二氯苯基)氨基]苯基乙酰氯1经在吡啶中用3,5-二溴邻氨基苯甲酸处理后与水合肼反应,然后进行乙酰化反应而合成的,由2- [2-(2,6-二氯苯基)氨基]苯基乙酰氯合成。这些化合物的结构已通过元素分析,IR和NMR光谱数据阐明。评价了标题化合物吡唑基-喹唑啉-4(3H)酮6a-m的体外抗菌和抗真菌活性。

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