Ligand‐Promoted Iron‐Catalyzed Nitrene Transfer for the Synthesis of Hydrazines and Triazanes through N‐Amidation of Arylamines

Author:

Zhu Shi‐Yang1ORCID,He Wen‐Ji1,Shen Guan‐Chi1ORCID,Bai Zi‐Qian1ORCID,Song Fang‐Fang1ORCID,He Gang1ORCID,Wang Hao1ORCID,Chen Gong123ORCID

Affiliation:

1. State Key Laboratory and Institute of Elemento-Organic Chemistry College of Chemistry Nankai University Tianjin 300071 China

2. Frontiers Science Center for New Organic Matter Nankai University Tianjin 300071 China

3. Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192 China

Abstract

AbstractHerein, we report that bulky alkylphosphines such as PtBu3 can switch the roles from actor to spectator ligands to promote the FeCl2‐catalyzed N‐amidation reaction of arylamines with dioxazolones, giving hydrazides in high efficiency and chemoselectivity. Mechanistic studies indicated that the phosphine ligands could facilitate the decarboxylation of dioxazolones on the Fe center, and the hydrogen bonding interactions between the arylamines and the ligands on Fe nitrenoid intermediates might play a role in modulating the delicate interplay between the phosphine ligand, arylamine, and acyl nitrene N, favoring N−N coupling over N−P coupling. The new ligand‐promoted N‐amidation protocols offer a convenient way to access various challenging triazane compounds via double or sequential N‐amidation of primary arylamines.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

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