Synthesis, Reaction and Antiviral Activity of 2,4-Diaryl-1,3-selenazoles

被引:9
作者
Al-Rubaie, Ali Z. [1 ]
Al-Masoudi, Wasfi A. [2 ,5 ]
Hameed, Ali Jameel [1 ]
Yousif, Lina Z. [1 ]
Graia, Mohsen [3 ,4 ]
机构
[1] Univ Basrah, Coll Sci, Dept Chem, Basrah, Iraq
[2] Al Mergab Univ, Coll Arts & Sci, Dept Chem, Tarhona, Libya
[3] Fac Sci Tunis, Lab Mate & Cristallochim, Tunis 2029, Tunisia
[4] Inst Preparatoire Etud Ingn Sfax, Sfax, Tunisia
[5] Al Mergab Univ, Coll Arts & Sci Tarhona, Dept Chem, Tarhona, Libya
来源
JOURNAL OF THE KOREAN CHEMICAL SOCIETY-DAEHAN HWAHAK HOE JEE | 2008年 / 52卷 / 01期
关键词
1,3-Selenazoles; arylselenocarboxamides; alpha-bromoketones; X-ray; HIV-1;
D O I
10.5012/jkcs.2008.52.1.036
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The cyclization of primary arylselenocarboxylic amides with a-bromoketones afforded a variety of new 2,4-diaryl-1,3-selenazoles. Halogenation of the 2,4-diaryl-1,3-selenazoles with chlorine, bromine and iodine gave the new 1,1-dihalo-2,4-diaryl-1,3-selenazoles in good yields. Antiviral activity of some 1,1-dihalo-2,4-diaryl-1,3-selenazoles has been tested against AIDS virus (HIV-1 and HIV-2). They showed some bioactivity against HIV-1. All compounds were characterized by their elemental analysis, H-1 NMR and mass spectroscopic data. The crystal structure of 2-(3,4dimethoxyphenyl)- 4-(4-bromophenyl)-1,3-selenazole displays the molecular configuration.
引用
收藏
页码:36 / 46
页数:11
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