SYNTHESIS AND ANTITUMOR ACTIVITY OF A SERIES OF BENZOFURYL-SUBSTITUTED 1,2,4-TRIAZOLES AND TRIAZOLIN-5-THIONES

被引:0
|
作者
Kaldrikyan, M. A. [1 ]
Grigoryan, L. A. [1 ]
Melik-Ogandzhanyan, R. G. [1 ]
Arsenyan, F. G. [1 ]
机构
[1] Natl Acad Sci Republ Armenia, AL Mndzhoyan Inst Fine Organ Chem, Sci Technol Ctr Organ & Pharmaceut Chem, Erevan, Armenia
关键词
Thiosemicarbazide; hydrazide; mercaptotriazole; S-alkylation; N-aminomethylation; triazolin-5-thiones;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
3-Benzofuryl-4-benzyl(cyclohexyl)-5-mercapto-1,2,4-triazoles were synthesized by cyclization of the corresponding substituted thiosemicarbazides. 5-Mercaptotriazoles were S-alkylated with various alkenyl-substituted benzylhalogenides, chloracetamide, chloroacetic, and alpha-bromopropionic and alpha-bromocaproic acids. The aminomethylation and hydroxymethylation reactions of 3-benzofuryl-4-benzyl(cyclohexyl)-5-mercapto-1,2,4-triazoles were studied. The antitumor activity of the resulting compounds was investigated.
引用
收藏
页码:211 / 214
页数:4
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