Rh(III)‐Catalyzed Selective C−H Alkylation and Alkenylation of 1,2,3‐Benzotriazinones with Maleimides

Author:

Xiao Lin1,Shen Dan‐Ting1,Zou Wen‐Xuan1,Song Jia‐Lin1,Wei Jiaohang1,Liu Xiang2ORCID,Zhang Shang‐Shi1ORCID,Zhang Luyong1

Affiliation:

1. Center for Drug Research and Development Guangdong Provincial Key Laboratory of Advanced Drug Delivery Guangdong Provincial Engineering Center of Topical Precise Drug Delivery System Guangdong Pharmaceutical University Guangzhou 510006 People's Republic of China

2. School of Chemistry and Chemical Engineering Guangdong Pharmaceutical University Zhongshan 528458 People's Republic of China

Abstract

AbstractHerein, we describe a reaction conditions‐based switchable Rh(III)‐catalyzed C−H alkylation and alkenylation of 1,2,3‐benzotriazinones with maleimides, where the triazinone serves as a directing group rather than its traditional role denitrogenative precursor. This strategy enables the selective synthesis of diverse 3‐arylated succinimides and 3‐arylated maleimides in up to 99% yield and a broad substrate scope (48 examples). Furthermore, for the first time, a tandem C−H alkylation and denitrogenative coupling of 1,2,3‐benzotriazinones has been achieved by slightly modifying the reaction conditions. Additionally, gram‐scale reactions and product derivatizations were conducted to demonstrate the synthetic utility.

Funder

National Natural Science Foundation of China

Guangdong Pharmaceutical University

Publisher

Wiley

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