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Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance

机译:6-硝基-1H-吲唑的2-氮杂环丁酮衍生物的合成及其生物学意义

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A new series of 3-chloro-1-{[2-(6-nitro-1H-indazol-1-yl)ethyl]amino}-4-(substituted phenyl)-2-azetidinones (4a-j) was synthesized in four steps from 6-nitro-1H-indazole and characterized by IR, 1H NMR, 13C NMR, FAB-mass spectrometry and chemical methods. Compounds 4(a-j) were screened in vitro for their antibacterial, antifungal and antitubercular activities against some selected microorganism and for their antiinflammatory activity (in vivo) against albino rats (either sex). All above activities of compounds 4(a-j) showed acceptable results.
机译:合成了一系列新的3-氯-1-{[2-(6-硝基-1H-吲唑-1-基)乙基]氨基} -4-(取代的苯基)-2-氮杂环丁烷酮(4a-j)。从6-硝基-1H-吲唑开始四个步骤,并通过IR,1H NMR,13C NMR,FAB质谱和化学方法进行表征。体外筛选化合物4(a-j)对某些选定微生物的抗菌,抗真菌和抗结核活性,以及​​对白化病大鼠(雌雄同体)的抗炎活性(体内)。化合物4(a-j)的所有上述活性显示出可接受的结果。

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