A convenient synthesis of 2-amino-1, 3-selenazoles using ionic liquid and microwave irradiation

M Maradolla, GVP Chandramouli

Index: Maradolla, Mohanbabu; Chandramouli Phosphorus, Sulfur and Silicon and the Related Elements, 2011 , vol. 186, # 8 p. 1650 - 1654

Full Text: HTML

Citation Number: 9

Abstract

Abstract A simple and environmentally benign synthesis of 2-amino-1, 3-selenazoles by microwave irradiation using 1-butyl-3-methylimidazolium tetrafluoroborate ([Bmim] BF4) ionic liquid (IL) is described. Acyl halides, phenacyl halides, and α-bromo-β-keto esters easily undergo condensation with selenourea in ([Bmim] BF4) by microwave irradiation to afford the desired products of good purity in excellent yields. The ionic liquid can be easily ...

Related Articles:

Synthesis of a series of novel 2, 4, 5-trisubstituted selenazole compounds as potential PLTP inhibitors

[Ling, Cui; Zheng, Zhibing; Jiang, Xian Cheng; Zhong, Wu; Li, Song Bioorganic and Medicinal Chemistry Letters, 2010 , vol. 20, # 17 p. 5123 - 5125]

The Reaction of Ketones with Iodine and Selenourea1

[King; Hlavacek Journal of the American Chemical Society, 1951 , vol. 73, p. 1864]

More Articles...