Domino Sonogashira coupling/metal carbene-involved annulation enabled by Pd/Cu relay catalysis: rapid assembly of indazole-containing biheteroaryls†

Ruiming Ding , Haili Cui , Yongyan Zhu , Yao Zhou , Huaming Tao , Shaoyu Mai
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Abstract

An efficient and novel method has been developed for the synthesis of indazole-containing biheteroaryls via a domino Sonogashira coupling/azaenyne cycloisomerization/Barton–Kellogg reaction. The new scalable protocol leads to a broad array of substituted indazole-containing biheteroaryls under mild reaction conditions. Compared to classical domino Sonogashira coupling/cyclization, this powerful strategy enables simultaneous generation of two heterocycles, especially the two C-atoms of a terminal alkyne are, respectively, incorporated into two different rings. Preliminary mechanistic studies demonstrate that the CuI catalyst has multiple roles, guaranteeing the connection of each reaction smoothly. Remarkably, this work represents an unprecedented example of domino Sonogashira coupling/metal carbene-involved annulation.

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Domino Sonogashira偶联/金属卡宾参与Pd/Cu中继催化的环化:含吲唑双杂芳基的快速组装†
通过domino Sonogashira偶联/氮茚环异构化/Barton–Kellogg反应,开发了一种合成含吲唑双杂芳基的高效新方法。新的可扩展方案在温和的反应条件下产生了广泛的含取代吲唑的双杂芳基。与经典的domino Sonogashira偶联/环化相比,这种强大的策略能够同时产生两个杂环,尤其是末端炔烃的两个C原子分别被结合到两个不同的环中。初步的机理研究表明,CuI催化剂具有多种作用,保证了每个反应的顺利连接。值得注意的是,这项工作代表了多米诺骨牌Sonogashira偶联/金属卡宾参与环空的一个前所未有的例子。
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