Multicomponent Approach for the Synthesis of Substituted 1,8-Naphthyridine Derivatives Catalyzed by N-Bromosulfonamides

被引:4
|
作者
Ghorbani-Vaghei, Ramin [1 ]
Malaekehpoor, Seyedeh Mina [1 ]
机构
[1] Bu Ali Sina Univ, Dept Organ Chem, Fac Chem, Hamadan 6517838683, Iran
来源
SYNTHESIS-STUTTGART | 2017年 / 49卷 / 04期
关键词
1,8-naphthyridine; N-brornosulfonamides; 2-aminopyridine; Knoevenagel/Michael addition; heterocyclization; MCR; ONE-POT SYNTHESIS; BIOLOGICAL EVALUATION; AGENTS; INHIBITORS; DESIGN; NAPHTHYRIDINES; SERIES;
D O I
10.1055/s-0036-1588886
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A single-step, facile synthesis of new 1 8-naphthyridine de rivatives was carried out at room temperature under mild conditions using a three-component condensation reaction of substituted 2-arninpyridines, malononitrile or methyl/ethyl cyanoacetate, and various aldehydes in the presence of N,N,N',N'-tetra bromobenzene-1,3-disulfonamide (TBBDA) or poly(N,N'-dibromo-N-ethylbenzene-1,3-disulfonarnide) (PBBS) as Lewis acid. A simple procedure, good to high yields, easy workup, and purification and reusability of the catalyst are significant advantages of this process.
引用
收藏
页码:763 / 769
页数:7
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