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Selective and Scalable Electrosynthesis of 2H‐2‐(Aryl)‐benzod‐123‐triazoles and Their N‐Oxides by Using Leaded Bronze Cathodes

机译:铅青铜电极选择性且可扩展地合成2H-2-(芳基)-苯并d -123-三唑及其氮氧化物

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摘要

Electrosynthesis of ‐2‐(aryl)benzo[ ]‐1,2,3‐triazoles and their N‐oxides from 2‐nitroazobenzene derivatives is reported. The electrolysis is conducted in a very simple undivided cell under constant current conditions with a leaded bronze cathode and a glassy carbon anode. The product distribution between ‐2‐(aryl)benzo[ ]‐1,2,3‐triazoles and their N‐oxides can be guided by simply controlling the current density and the amount of the charge applied. The reaction tolerates several sensitive functional groups in reductive electrochemistry. The usefulness and the applicability of the synthetic method is demonstrated by a formal synthesis of an antiviral compound.
机译:据报道由2-硝基偶氮苯衍生物电合成-2-(芳基)苯并[] -1,2,3-三唑及其N-氧化物。电解是在一个非常简单的不分隔电池中,在恒定电流条件下,使用铅青铜阴极和玻璃碳阳极进行的。通过简单地控制电流密度和施加的电荷量,可以指导-2-芳基苯并[] -1,2,3-三唑与它们的N氧化物之间的产物分布。该反应耐受还原电化学中的几个敏感官能团。通过抗病毒化合物的正式合成证明了合成方法的有用性和适用性。

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