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HERO ID
8443782
Reference Type
Journal Article
Title
æ°´ç¸ä¸å¯è§å ä¸è¯ç²éæ°§ååæå¹ååé ®è¡çç©çç ç©¶
Author(s)
Zhang, F; Hou, H; Xu, X; Chen, Z; Ke, F
Year
2021
Is Peer Reviewed?
1
Journal
Youji Huaxue / Chinese Journal of Organic Chemistry
ISSN:
0253-2786
Publisher
Science Press
Volume
41
Issue
2
Page Numbers
833-841
Language
Chinese
DOI
10.6023/cjoc202007027
Abstract
A novel visible-light-introduced reaction for the construction of quinazolinone derivatives via radical cyclization of 2-aminobenzamides with benzyl alochols under water phase has been developed. The reaction has been achieved in high yield under mild conditions by using I2 as photocatalyst, which is cheap, available and easy to handle. A variety of quinazolinones were obtained in yields up to 92%. It might provide a promising protocol for the synthesis of quinazolinone derivatives. Its application was performed by the synthesis of N-(2-fluoro-5-methylphenyl)-6-(2, 2, 2-trifluoroethoxy)pteridin-4-amine, which displayed significant inhibitory activity. © 2021 Chinese Chemical Society & SIOC, CAS.
Keywords
Catalyst; Iodine; Oxidant; Quinazolinone; Visible light
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