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Iridium(III)-Catalyzed Regioselective C7-Amination of N-Pivaloylindoles with Sulfonoazides

机译:铱(III)与磺酰叠氮化物催化N-吡咯烷基吲哚的区域选择性C7胺化

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摘要

Direct C7-amination of N-pivaloylindoles has been achieved using a combination of [Cp*IrCl2](2), AgNTf2, and AgOAc as the catalyst and sulfonoazides as the nitrogen source. The reaction proceeded at room temperature to 80 degrees C to afford 7-sulfonamidoindoles in good to excellent yields. The reaction is broadly applicable to the C7-amination of a wide variety of 3-, 4-, 5-, and 6-substituted N-pivaloylindoles with either alkyl or aryl sulfonoazides.
机译:使用[Cp * IrCl2](2),AgNTf2和AgOAc作为催化剂,磺酰叠氮化物作为氮源的组合,可以实现N-吡咯咯啉直接C7胺化反应。反应在室温至80℃下进行,以良好至优异的产率得到7-磺酰胺基吲哚。该反应广泛地适用于各种3-,4-,5-和6-取代的N-吡咯烷基吲哚与烷基或芳基磺酰叠氮的C7胺化反应。

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