研究论文

Na2S2O8介导的咪唑并[1,2-α]吡啶与杂芳胺在无金属条件下的C—H胺化反应

  • 孙一平 ,
  • 陈德茂 ,
  • 何玲 ,
  • 王祖利
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  • a 中国科学院兰州化学物理研究所 固体润滑国家重点实验室 兰州 730000
    b 青岛农业大学化学与药学院 青岛 266109
    c 重庆大学药学院创新药物研究中心 天然产物合成与药物研究重庆重点实验室 重庆 401331

收稿日期: 2023-11-24

  修回日期: 2024-01-02

  网络出版日期: 2024-01-12

基金资助

国家自然科学基金(21772107); 山东省高等学校青创人才引育计划(2021)

Na2S2O8 Mediated C—H Amination of Imidazo[1,2-α]pyridines with Heteroaromatic Amines under Metal-Free Conditions

  • Yiping Sun ,
  • Demao Chen ,
  • Ling He ,
  • Zuli Wang
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  • a State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000
    b College of Chemistry and Pharmaceutical Sciences, Qingdao Agricultural University, Qingdao 266109
    c Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, Innovative Drug Research Center, School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331

Received date: 2023-11-24

  Revised date: 2024-01-02

  Online published: 2024-01-12

Supported by

National Natural Science Foundation of China(21772107); Youth Innovation Team Project for Talent Introduction and Cultivation in Universities of Shandong Province(2021)

摘要

发展了一种高效实用的氨化咪唑[1,2-α]吡啶类化合物的方法. 值得注意的是, 该反应无需任何金属催化剂参与. 在中等至高收率下, 成功得到了带有多样取代基的产物.

本文引用格式

孙一平 , 陈德茂 , 何玲 , 王祖利 . Na2S2O8介导的咪唑并[1,2-α]吡啶与杂芳胺在无金属条件下的C—H胺化反应[J]. 有机化学, 2024 , 44(5) : 1667 -1674 . DOI: 10.6023/cjoc202311026

Abstract

A highly efficient and practical amination protocol for imidazo[1,2-α]pyridines using heteroaromatic amines was developed. Notably, the transformation proceeds without the need for any metal catalyst. Isolation of products bearing diverse substituents was achieved in moderate to high yields.

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