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Synthesis of novel 2-quinolone derivatives

机译:新型2-喹诺酮衍生物的合成

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In this work, N-amino quinoline-2-one (2) has been synthesized by the reflux of coumarin (1) with hydrazine hydrate (99%) in ethanol for 12 h. The azomethines (3-6) were prepared from the corresponding aryl aldehydes and ketones. Tetrazine derivative (7) was prepared from the reaction of compound (2) with CS2 and hydrazine hydrate in the presence of potassium hydroxide. However, the reaction of compound (2) with thiol compounds afforded the derivatives (8-14).Finally, condensation of compound (11) with 4-hydroxy benzaldehyde brought about the derivative (15).The structures of the synthesized compounds were deduced by using some spectroscopic methods, FT-IR, UV-Visible and NMR.
机译:在这项工作中,通过将香豆素(1)与水合肼(99%)在乙醇中回流12小时,合成了N-氨基喹啉-2-酮(2)。由相应的芳基醛和酮制备偶氮甲碱(3-6)。在氢氧化钾的存在下,由化合物(2)与CS 2和水合肼的反应制备四嗪衍生物(7)。然而,化合物(2)与硫醇化合物反应得到衍生物(8-14)。最后,化合物(11)与4-羟基苯甲醛缩合生成衍生物(15),推导了合成化合物的结构通过使用一些光谱方法,FT-IR,UV-Visible和NMR。

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