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A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters from chromone and isatin.
Wang, Xuequan; Yang, Zhixin; Miu, Weihang; Ye, Pingting; Bai, Mengjiao; Duan, Suyue; Shen, Xianfu.
Affiliation
  • Wang X; Key Laboratory of Natural Pharmaceutical and Chemical Biology of Yunnan Province, School of Science, Honghe University Mengzi Yunnan 661100 China huolixuanfeng@126.com.
  • Yang Z; Key Laboratory of Natural Pharmaceutical and Chemical Biology of Yunnan Province, School of Science, Honghe University Mengzi Yunnan 661100 China huolixuanfeng@126.com.
  • Miu W; Key Laboratory of Natural Pharmaceutical and Chemical Biology of Yunnan Province, School of Science, Honghe University Mengzi Yunnan 661100 China huolixuanfeng@126.com.
  • Ye P; Key Laboratory of Natural Pharmaceutical and Chemical Biology of Yunnan Province, School of Science, Honghe University Mengzi Yunnan 661100 China huolixuanfeng@126.com.
  • Bai M; Key Laboratory of Natural Pharmaceutical and Chemical Biology of Yunnan Province, School of Science, Honghe University Mengzi Yunnan 661100 China huolixuanfeng@126.com.
  • Duan S; Key Laboratory of Natural Pharmaceutical and Chemical Biology of Yunnan Province, School of Science, Honghe University Mengzi Yunnan 661100 China huolixuanfeng@126.com.
  • Shen X; Center for Yunnan-Guizhou Plateau Chemical Functional Materials and Pollution Control, Qujing Normal University 655011 P. R. China.
RSC Adv ; 9(63): 37057-37060, 2019 Nov 11.
Article in En | MEDLINE | ID: mdl-35539051
A simple and convenient synthesis of 3-salicyloylquinoline-4-carboxylic esters has been developed through an AlCl3-catalyzed reaction of easily available Baylis-Hillman adducts from chromones and isatin-derivatives. This reaction involves esterification, cyclization and ring opening in a one-step process, and provides an efficient approach for easy access to a series of valuable salicyloylquinoline derivatives with high yields. Moreover, this protocol offers several advantages, such as availability of starting materials, economic availability, operational simplicity and mild reaction conditions.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2019 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2019 Document type: Article Country of publication: United kingdom