A versatile approach for one-pot synthesis of hybridized quinolines linked to fused N-containing heterocycles in water

被引:1
作者
Rezvanian, Atieh [1 ]
Khodadadi, Behnoosh [1 ]
Tafreshi, Sepideh [1 ]
Shiri, Pezhman [2 ]
机构
[1] Alzahra Univ, Fac Chem, Dept Organ Chem, Tehran, Iran
[2] Shiraz Univ Med Sci, Sch Adv Med Sci & Technol, Dept Med Nanotechnol, Shiraz, Iran
关键词
Green chemistry; Quinoline-based products; Multicomponent reaction; Hybrid organic compounds; Water-based reactions; Diastereoselective synthesis; MULTICOMPONENT REACTIONS; C-C; DERIVATIVES; STRATEGY; 1,2,3-TRIAZOLES; SOLVENTS; CATALYST; COMPLEX;
D O I
10.1007/s11030-023-10719-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here, highly efficient one-pot protocols for the synthesis of structurally diverse fused N-containing heterocycles containing 2-chloroquinoline employing 1,1-bis(methylsulfanyl)-2-nitroethene, diamines, 2-chloroquinoline-3-carbaldehydes and dimedone/Meldrum's acid in green media in the absence of catalyst are reported. The current report proposes sustainable, simple, four-component and straightforward strategies for generating interesting N-containing heterocyclic compounds from a range of diamines and 2-chloroquinoline-3-carbaldehydes. The utilization of water as green media furnishes sustainability by preventing the usage of toxic solvent. A range of quinoline-containing aldehydes and diamines can be converted to two types of products with respect to using dimedone or Meldrum's acid via an inexpensive, one-pot and easy route.
引用
收藏
页码:197 / 207
页数:11
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