Issues

 / 

2024

 / 

vol. 22 / 

issue 2

 



Download the full version of the article (in PDF format)

MARYAM ASHOUR, FAROUK KANDIL, and ABDULKADER ALAZRAK

Synthesis and Spectroscopic Characterization Study of Some Schiff Bases 1,3[N,N-Bis(5-Methyl-1,3,4-Triazole-2-Thione)] Benzene and 1,4[N,N-Bis(5-Methyl-1,3,4-Triazole-2-Thione)] Benzene
457–467 (2024)

PACS numbers: 61.05.Qr, 78.30.Jw, 81.07.Nb, 81.16.Be, 82.56.Ub

Some of triazole derivatives are synthesized by cyclization reaction of thiocarbohydrazide synthesized by reaction of carbon disulphide and aqueous hydrazine; the basic nucleus 3-methyl-4-amino-1,2,4-triazole-5-thione (L) is prepared by reaction of thiocarbohydrazide compound with glacial acetic acid under reflux condition. The compound (L) is subjected to addition reaction with different aldehydes to synthesize Schiff bases 1,3[N,N-Bis(5-methyl-1,3,4-triazole-2-thione)] benzene (L1) and 1,4[N,N-Bis(5-methyl-1,3,4-triazole-2-thione)] benzene (L2). The compounds (L1) and (L2) are confirmed by means of their melting point, FTIR, UV-visible, and 1H-NMR spectra

KEY WORDS: synthesis, Schiff bases, thiocarbohydrazide, triazole derivatives

DOI:  https://doi.org/10.15407/nnn.22.02.457

REFERENCES
  1. N. Mohamed Wannas, A. A. S. Al-Hamdani, and W. Al Zoubi, J. Phys. Org. Chem., 33, No. 11: 1 (2020); doi:10.1002/poc.4099
  2. M. S. Kasare, P. P. Dhavan, B. L. Jadhav, and S. D. Pawar, Chemistry Select, 4, No. 36: 10792 (2019); doi:10.1002/slct.201901605
  3. M. J. Kareem, A. A. S. Al-Hamdani, V. Y. Jirjees, M. E. Khan, A. W. Allaf, and W. Al Zoubi, J. Phys. Org. Chem., 34, No. 3: 1 (2021); doi:10.1002/poc.4156
  4. M. J. Kareem, A. A. S. Al-Hamdani, Y. G. Ko, W. Al Zoubi, and S. G. Mohammed, J. Mol. Struct., 1231: (2021); doi:10.1016/j.molstruc.2020.129669
  5. B. Shirinkam, M. Tabatabaee, B. M. Kukovec, C. L. Oliver, and M. Ghassemzadeh, Monatshefte f?r Chemie, 145, No. 11: 1753 (2014); doi:10.1007/s00706-014-1256-z
  6. Grace E. Iniama and Ededet A. Eno, Int. J. Eng. Sci. Math., 7, No. 9: 21 (2018); https://ijesm.co.in/uploads/68/5732_pdf.pdf
  7. M. T. Ghaneian et al., Pharm. Chem. J., 49, No. 3: 210 (2015); doi:10.1007/s11094-015-1258-0
  8. M. K. Bharty et al., Polyhedron, 173: 114125 (2019); doi:10.1016/j.poly.2019.114125
  9. J. W. Dhore, G. B. Pethe, S. P. Wagh, and G. D. Thorat, Arch. Appl. Sci. Res., 3, No. 1: 407 (2011); https://www.researchgate.net/publication/267996413_Synthesis_Characterization_and_Biological_Studies_of_Some_Triazolyl_Isonicotinamide
  10. Mohammad Al-Amin and M. Rabiul Islam, Journal of the Bangladesh Pharmacological Society (BDPS), 1: 21 (2006); doi:10.3329/bjp.v1i1.483
  11. L. F. Audrieth and P. G. Gordon, J. Org. Chem., 20, No. 2: 244 (1955); doi:10.1021/jo01120a015
  12. E. A. E. El-helw, H. A. Sallam, and A. S. Elgubbi, Synth. Commun., 49, No. 20: 2651 (2019); doi:10.1080/00397911.2019.1638938
  13. N. Naasani, J. Harbali, and F. Kandil, J. Pharm. Tech., 13, No. 10: 4565 (2020); doi:10.5958/0974-360X.2020.00804.5
  14. T. Paul, F. Hossen, and M. Haque, Asian J. Appl. Chem. Res., 5, No. 3: 39 (2020); doi:10.9734/AJACR/2020/v5i330138
  15. R. K. H. Al-daffay, Baghdad Sci. J., 7: 121 (2022); doi:10.21123/bsj.2022.6709
  16. Shaima Mohammed Reda and Abbas Ali Salih Al-Hamdani, Chemical Methodologies, 6: 475 (2022); doi:10.22034/CHEMM.2022.335815.1468
Creative Commons License
This article is licensed under the Creative Commons Attribution-NoDerivatives 4.0 International License
©2003—2024 NANOSISTEMI, NANOMATERIALI, NANOTEHNOLOGII G. V. Kurdyumov Institute for Metal Physics of the National Academy of Sciences of Ukraine.

E-mail: tatar@imp.kiev.ua Phones and address of the editorial office About the collection User agreement