Facile access to quinazolin-4(3<i>H</i>)-ones by tandem Cu-catalyzed annulation of 2-nitrobenzonitrile and alcohols under air

A convenient Cu-catalyzed synthesis of 2-arylquinazolin-4(3<i>H</i>)-one derivatives has been developed from simple starting materials such as 2-nitrobenzonitriles and alcohols under mild conditions. This procedure showed a broad substrate scope and tolerance of functional groups, high yields, and no need to use oxidants or reductants, making synthesis simple, convenient, and sustainable. Our methodology may be utilized for the one-pot synthesis of glycosminine alkaloid.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra01550b
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.00

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Facile access to quinazolin-4(3H)-ones by tandem Cu-catalyzed annulation of 2-nitrobenzonitrile and alcohols under air

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Quinazolinone synthesis and applications
article

Facile access to quinazolin-4(3H)-ones by tandem Cu-catalyzed annulation of 2-nitrobenzonitrile and alcohols under air

Tuan Thanh Dang, Hien Nguyen, Ban Van Phuc, Quoc Anh Ngo, Xuan Thai Vu, Minh Hoang Nguyen, Thùy Linh Nguyễn, Tan Van Nguyen, Tran Quang Hung, Nguyen Quang An
article en

Abstract

A convenient Cu-catalyzed synthesis of 2-arylquinazolin-4(3<i>H</i>)-one derivatives has been developed from simple starting materials such as 2-nitrobenzonitriles and alcohols under mild conditions. This procedure showed a broad substrate scope and tolerance of functional groups, high yields, and no need to use oxidants or reductants, making synthesis simple, convenient, and sustainable. Our methodology may be utilized for the one-pot synthesis of glycosminine alkaloid.

RSC AdvancesVol. 15(32)
Hanoi National University of Education (VN), VNU University of Science (VN), Vietnam Academy of Science and Technology (VN)
Vietnam Academy of Science and Technology
Openalex Percentile: Top 87%
Quinazolinone synthesis and applications
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