Synthesis and antitumor activity of 2-N- and 3-S-substituted 5-[2-(4-)benzyloxyphenyl]-1,2,4-triazoles and acylhydrazides

3-Thio-4-phenyl-5-[2-(4-)benzyloxyphenyl]-1,2,4-triazoles were prepared by cyclization of the corresponding thiosemicarbazides in alkaline medium. The 2- N -substituted derivatives of the aforementioned triazoles were obtained via aminomethylation, cyanethylation, and alkylation of α-epoxides. 3- S...

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Veröffentlicht in:Pharmaceutical chemistry journal 2012-12, Vol.46 (9), p.531-535
Hauptverfasser: Grigoryan, L. A., Kaldrikyan, M. A., Melik-Ogandzhanyan, R. G., Arsenyan, F. G.
Format: Artikel
Sprache:eng
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Zusammenfassung:3-Thio-4-phenyl-5-[2-(4-)benzyloxyphenyl]-1,2,4-triazoles were prepared by cyclization of the corresponding thiosemicarbazides in alkaline medium. The 2- N -substituted derivatives of the aforementioned triazoles were obtained via aminomethylation, cyanethylation, and alkylation of α-epoxides. 3- S -Substituted 1,2,4-triazoles were synthesized by alkylation with various aliphatic and aromatic halides. Acylhydrazides were prepared via reaction of 2-(4-)benzyloxybenzoic acid hydrazides with dicarboxylic acid anhydrides. The antitumor activity of the synthesized compounds was studied.
ISSN:0091-150X
1573-9031
DOI:10.1007/s11094-012-0840-y