Synthesis and Antitumor Activity of 2-N-,3-S-Substituted 5-(4-Benzyloxyphenyl)-1,2,4-Triazoles


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Аннотация

Cyclization of substituted thiosemicarbazides in alkaline medium was used to synthesize the corresponding 3-thio-4-benzyl(cyclohexyl, allyl)-5-(4-benzyloxyphenyl)-1,2,4-triazoles. These compounds were 3-S-alkylated with ethylene chlorohydrin, chloroacetamide, 3-bromo-4-methoxybenzyl chloride, and chloroacetic, 2-bromopropionic, and 2-bromocaproic acids. Aminomethylation and oxymethylation reactions were studied. 2-N-Aminomethylene and 2-N-oxymethylenetriazoline-3-thiones were prepared. The antitumor activity of the compounds synthesized here were studied.

Авторлар туралы

M. Kaldrikyan

A. L. Mndzhoyan Institute of Fine Organic Chemistry, Scientific-Technical Center for Organic and Pharmaceutical Chemistry, National Academy of Sciences of the Republic of Armenia

Email: chem@folium.ru
Армения, 26 Azatutyan Prospekt, Erevan, 0014

R. Melik-Ohanjanyan

A. L. Mndzhoyan Institute of Fine Organic Chemistry, Scientific-Technical Center for Organic and Pharmaceutical Chemistry, National Academy of Sciences of the Republic of Armenia

Email: chem@folium.ru
Армения, 26 Azatutyan Prospekt, Erevan, 0014

F. Arsenyan

A. L. Mndzhoyan Institute of Fine Organic Chemistry, Scientific-Technical Center for Organic and Pharmaceutical Chemistry, National Academy of Sciences of the Republic of Armenia

Email: chem@folium.ru
Армения, 26 Azatutyan Prospekt, Erevan, 0014

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