4.8 Article

Copper-Mediated ortho-C-H Amination Using DMF as the Amine Source

期刊

ORGANIC LETTERS
卷 23, 期 21, 页码 8505-8509

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c03223

关键词

-

资金

  1. Shanghai Institute of Materia Medica
  2. Chinese Academy of Sciences
  3. National Natural Science Foundation of China [21772211, 21920102003]
  4. Youth Innovation Promotion Association CAS [2014229, 2018293]
  5. Institutes for Drug Discovery and Development, Chinese Academy of Sciences [CASIMM0120163006]
  6. Science and Technology Commission of Shanghai Municipality [17JC1405000, 21ZR1475400, 18431907100]
  7. Program of Shanghai Academic Research Leader [19XD1424600]
  8. National Science & Technology Major Project Key New Drug Creation and Manufacturing Program, China [2018ZX09711002-006]
  9. China Postdoctoral Science Foundation [2019M662854]

向作者/读者索取更多资源

A copper-mediated ortho-C-H amination of anilines using oxalamide as the directing group and DMF as the amination reagent is reported in this study. The protocol shows good heterocyclic compatibility and synthetic practicality, with mechanistic experiments suggesting a radical pathway may be involved in the reaction.
We report herein a copper-mediated ortho-C-H amination of anilines using oxalamide as the directing group and DMF as the amination reagent. This protocol tolerates various functional groups and shows good heterocyclic compatibility. Late-stage dimethylamination of drugs demonstrated the synthetic practicality of the protocol. Mechanistic experiments indicate that a radical pathway may be involved in the reaction.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据