One-Pot Synthesis of Quinazoline-4(3<i>H</i>)-ones through Electrochemically Induced Three-Component Cyclization

This research introduces an electrochemically induced one-pot reaction designed for a three-component system to synthesize quinazolinone derivatives using isatoic anhydride, styrene, and hydrochloride amine as the starting substrates. Importantly, this reaction can be conducted in the absence of metal catalysts or oxidizing agents and exclusively relies on electrochemical redox mechanisms. Key advantages include the use of readily accessible raw materials, simple operational procedures, environmental sustainability, and high atomic efficiency. Lastly, reactions conducted on a gram scale illustrated the considerable practical applicability of this method.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-09-12
DOI
https://doi.org/10.1021/acs.joc.5c01177
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
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article

One-Pot Synthesis of Quinazoline-4(3H)-ones through Electrochemically Induced Three-Component Cyclization

Jing‐Wen Sun, Hao Zhang, Ming Bu, Yuge Ran et al.
1 links
The Journal of Organic Chemistry
Quinazolinone synthesis and applications
article

One-Pot Synthesis of Quinazoline-4(3H)-ones through Electrochemically Induced Three-Component Cyclization

Jing‐Wen Sun, Hao Zhang, Ming Bu, Yuge Ran, Haiyan Zhang, Jiahui Zhang, Hai‐Jun Wang, Huiying Liu, Lei Liu
article en

Abstract

This research introduces an electrochemically induced one-pot reaction designed for a three-component system to synthesize quinazolinone derivatives using isatoic anhydride, styrene, and hydrochloride amine as the starting substrates. Importantly, this reaction can be conducted in the absence of metal catalysts or oxidizing agents and exclusively relies on electrochemical redox mechanisms. Key advantages include the use of readily accessible raw materials, simple operational procedures, environmental sustainability, and high atomic efficiency. Lastly, reactions conducted on a gram scale illustrated the considerable practical applicability of this method.

The Journal of Organic ChemistryVol. 90(38)
Institute of the North (US), Qiqihar Medical University (CN)
Openalex Percentile: Top 82%
Quinazolinone synthesis and applications
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