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Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions

机译:通过Domino,“点击”和RDA反应,合成含有1,2,3-三唑环系统的新型N-杂环化合物

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摘要

An uncomplicated, high-yielding synthetic route has been developed to constitute complicated heterocycles, applying domino, click and retro-Diels⁻Alder (RDA) reaction sequences. Starting from 2-aminocarboxamides, a new set of isoindolo[2,1-a]quinazolinones was synthesized with domino ring closure. A click reaction was performed to create the 1,2,3-triazole heterocyclic ring, followed by an RDA reaction resulting in dihydropyrimido[2,1-a]isoindole-2,6-diones. The absolute configuration, concluded by the norbornene structure that served as a chiral source, remained constant throughout the transformations. The structure of the synthesized compounds was examined by 1H and 13C Nuclear Magnetic Resonance (NMR) methods.
机译:已经开发了一种简单的高产的合成途径来构成复杂的杂环,施用Domino,点击和ryro-diels⁻alder(RDA)反应序列。从2-氨基羧酰胺开始,用多米诺圆环封闭合成一组新的异丙醇[2,1-a]喹唑啉酮。进行咔哒反应以产生1,2,3-三唑杂环环,然后进行RDA反应,得到二氢嘧啶[2,1-A]异吲哚-2,6-硫酮。通过用作手性源的降冰片烯结构结束的绝对配置,在整个转化过程中保持不变。通过1H和13C核磁共振(NMR)方法检查合成化合物的结构。

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