A Novel Green Synthesis of Thalidomide and Analogs

被引:11
|
作者
Benjamin, Ellis [1 ]
Hijji, Yousef M. [2 ]
机构
[1] Stockton Univ, Dept Chem, 101 Vera King Farris Dr, Galloway, NJ 08205 USA
[2] Qatar Univ, Dept Chem & Earth Sci, POB 2713, Doha, Qatar
关键词
MULTIPLE-MYELOMA; TNF-ALPHA; LENALIDOMIDE MAINTENANCE; EXPRESSION; POMALIDOMIDE; ANTICANCER; IL-1-BETA; IL-10; CELLS; DRUG;
D O I
10.1155/2017/6436185
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thalidomide and its derivatives are currently under investigation for their antiangiogenic, immunomodulative, and anticancer properties. Current methods used to synthesize these compounds involve multiple steps and extensive workup procedures. Described herein is an efficient microwave irradiation green synthesis method that allows preparation of thalidomide and its analogs in a one-pot multicomponent synthesis system. The multicomponent synthesis system developed involves an array of cyclic anhydrides, glutamic acid, and ammonium chloride in the presence of catalytic amounts of 4-N, N-dimethylaminopyridine (DMAP) to produce thalidomide and structurally related compounds within minutes in good isolated yields.
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页数:6
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