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首页> 外文期刊>International Journal of Bio-Inorganic Hybrid Nanomaterials >A Facile One-Pot Solvent-Free Synthesis of 1,2-Dihydro-1-arylnaphtho [1,2-e] [1,3] oxazine-3-ones Catalyzed by Nano-Fe2O3
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A Facile One-Pot Solvent-Free Synthesis of 1,2-Dihydro-1-arylnaphtho [1,2-e] [1,3] oxazine-3-ones Catalyzed by Nano-Fe2O3

机译:纳米Fe2O3催化简便无溶剂合成1,2-二氢-1-芳基萘[1,2-e] [1,3]恶嗪-3-酮

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One of the most important goals in medicinal chemistry is the development of new techniques and new heterocyclic compounds with pharmaceutical activity. The present study aimed to use a method for the synthesis of some 1,2-Dihydro-1-arylnaphtho [1,2-e] [1,3] oxazine-3-ones. The question this study tried to answer was this reaction can be performed in present of nano-Fe2O3 as an acid catalyst and solvent-free conditions or not. Therefore, to find answer to the question, some of the1,2-Dihydro-1-arylnaphtho [1,2-e] [1,3] oxazine-3-one derivatives with medicinal properties were synthesized with rapid, high yield, novel, facile, and one-pot condensation of β-naphthol, aromatic aldehydes and urea using by nano-Fe2O3 under solvent-free conditions. The one-pot synthesis on solid inorganic support provides the products in good yields. The synthesized some of oxazine-3-one derivatives has been reported.Nano-Fe2O3 was reused for four runs without significant loss of activity and the effect of the solvents on the model reaction was carried out in various solvents.
机译:药物化学最重要的目标之一是开发具有药物活性的新技术和新杂环化合物。本研究旨在使用一种方法合成一些1,2-二氢-1-芳基萘[1,2-e] [1,3]恶嗪-3-酮。这项研究试图回答的问题是,该反应是否可以在作为酸催化剂的纳米Fe2O3的存在和无溶剂条件下进行。因此,为了找到问题的答案,合成了一些具有药用特性的1,2-二氢-1-芳基萘[1,2-e] [1,3]恶嗪-3-酮衍生物,它们具有快速,高收率,新颖的特点。纳米Fe2O3在无溶剂条件下,可轻松,轻松地一锅浓缩β-萘酚,芳族醛和尿素。在固态无机载体上进行一锅法合成可提供高收率的产品。已经报道了一些恶嗪-3-酮衍生物的合成。纳米Fe2O3在没有明显活性损失的情况下重复使用了四次,并且在各种溶剂中进行了溶剂对模型反应的影响。

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