Synthesis and antitumor activity of a series of benzofuryl-substituted 1,2,4-triazoles and triazolin-5-thiones

  • M. A. Kaldrikyan
  • L. A. Grigoryan
  • R. G. Melik-Ogandzhanyan
  • F. G. Arsenyan
Article

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 α-bromopropionic and α-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.

Key words

Thiosemicarbazide hydrazide mercaptotriazole S-alkylation N-aminomethylation triazolin-5-thiones 

References

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Copyright information

© Springer Science+Business Media, Inc. 2011

Authors and Affiliations

  • M. A. Kaldrikyan
    • 1
  • L. A. Grigoryan
    • 1
  • R. G. Melik-Ogandzhanyan
    • 1
  • F. G. Arsenyan
    • 1
  1. 1.ErevanArmenia

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