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首页> 外文期刊>Synthetic Communications >Water-Mediated Selective Synthesis of Pyrazolo[1,5-a]quinazolin-5(4H)-ones and [1,2,4]Triazolo[1,5-a]quinazolin-5(4H)-one via Copper-Catalyzed Cascade Reactions
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Water-Mediated Selective Synthesis of Pyrazolo[1,5-a]quinazolin-5(4H)-ones and [1,2,4]Triazolo[1,5-a]quinazolin-5(4H)-one via Copper-Catalyzed Cascade Reactions

机译:水催化铜催化选择性合成吡唑并[1,5-a]喹唑啉-5(4H)-one和[1,2,4]三唑并[1,5-a]喹唑啉-5(4H)-one级联反应

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摘要

A convenient and sustainable synthesis of pyrazolo[1,5-a]quinazolin-5(4H)-ones and [1,2,4]triazolo[1,5-a]quinazolin-5(4H)-one through copper-catalyzed cascade reactions of 2-bromobenzoates with 1H-pyrazol-5-amines or 1H-1,2,4-triazol-5-amine under ligand-free conditions in water is presented. It is notable that aqueous medium turned out to be crucial for the chemoselective formation of the title compounds. Compared with literature protocols, this new method showed advantages such as simple and sustainable procedure, commercially available starting materials, and convenient reuse of the reaction medium together with the copper catalyst.
机译:通过铜催化方便且可持续地合成吡唑并[1,5-a]喹唑啉-5(4H)-和[1,2,4]三唑并[1,5-a]喹唑啉-5(4H)-提出了2-溴苯甲酸酯与1H-吡唑-5-胺或1H-1,2,4-三唑-5-胺在无水条件下的级联反应。值得注意的是,水性介质对于标题化合物的化学选择性形成至关重要。与文献方法相比,该新方法显示出诸如简单且可持续的步骤,可商购的原料以及反应介质与铜催化剂一起方便重用的优点。

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