Synthesis and Biological activity of 1,3-Thiazolylidenehydrazinylidene ethylpyridiniumbromide monohydrate, 1,3-Thiazolylidenehydraziniumbromide and 1,3-Thiazolylidenehydrazine derivatives

Authors

  • Alaa A. Hassan Minia University, El-Minia 61519,
  • Shaaban K. Mohamed Chemistry and Environment Division, Manchester Metropolitan University, Manchester, MI5GD
  • Nasr K. Mohamed Minia University, El-Minia 61519,
  • Kamal M. A. El-Shaieb Minia University, El-Minia 61519,
  • Ahmed T. Abdel-Aziz Minia University, El-Minia 61519
  • Marwa Rageh Abdel Rahman Botany Department, Faculty of Science, Sohag University, 82524 Sohag

DOI:

https://doi.org/10.24297/jac.v11i3.863

Keywords:

Substituted ethylidenehydrazinecarbothioamides, 1-aryl-2-bromoethanones, 1, 3-thiazolylidene-hydrazine derivatives and their salts, anti-bacterial activity.

Abstract

1,3-Thiazolylidenehydrazinylidene ethylpyridinium bromide monohydrate, 1,3-thiazolylidenehydrazinium bromide and 1,3-thiazolylidenehydrazine derivatives were synthesized by heterocyclization of 2-(1-substituted ethylidene) hydrazinecarbothioamides, characterized and screened for their anti-bacterial activities. The structures of synthesized compounds were established by spectroscopic (IR, 1H, 13C-NMR, Mass) and X-ray analyses.

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Author Biographies

Alaa A. Hassan, Minia University, El-Minia 61519,

Chemistry Department, Faculty of Science

Nasr K. Mohamed, Minia University, El-Minia 61519,

Chemistry Department, Faculty of Science

Kamal M. A. El-Shaieb, Minia University, El-Minia 61519,

Chemistry Department, Faculty of Science

Ahmed T. Abdel-Aziz, Minia University, El-Minia 61519

Chemistry Department, Faculty of Science

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Published

2015-04-03

How to Cite

Hassan, A. A., Mohamed, S. K., Mohamed, N. K., El-Shaieb, K. M. A., Abdel-Aziz, A. T., & Rahman, M. R. A. (2015). Synthesis and Biological activity of 1,3-Thiazolylidenehydrazinylidene ethylpyridiniumbromide monohydrate, 1,3-Thiazolylidenehydraziniumbromide and 1,3-Thiazolylidenehydrazine derivatives. JOURNAL OF ADVANCES IN CHEMISTRY, 11(3), 3357–3366. https://doi.org/10.24297/jac.v11i3.863

Issue

Vol. 11 No. 3 (2015)

Section

Articles

License

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