Synthesis and properties of some S-derivatives of 4-phenyl-5-((5-phenylamino-1,3,4-thiadiazole-2-ylthio)methyl)-1,2,4-triazole-3-thione

Authors

  • A. S. Hotsulia Zaporizhzhіa State Medical University, Ukraine,
  • S. O. Fedotov Zaporizhzhіa State Medical University, Ukraine,

DOI:

https://doi.org/10.14739/2409-2932.2019.3.184170

Keywords:

thiadiazole, 1, 2, 4-triazole, physical-chemical properties, screening studies

Abstract

 Studies in the field of chemistry and pharmacology of derivatives of thiadiazole and 1,2,4-triazole are promising and relevant, which is associated with significant success in creating new drugs based on them. The combination of these heterocycles in one molecule makes it possible to increase the probability of detecting substances with a certain type of biological activity among the synthesized compounds.The aim of the work was to optimize the synthesis and study of the properties of S-alkyl derivatives of 5-R-4-phenyl-1,2,4-triazole-3-thione, containing a thiadiazole fragment in their structure, as well as the prediction of possible biological activity to rating the prospects of further studies in vivo and in vitro.Materials and methods. As a key starting reagent, 3-amino-1-phenylthiourea was used. Using the reaction between the starting reagent and carbon disulfide in DMF, thion was obtained, which was further alkylated with isopropyl chloroacetate. The resulting reaction product was then used for subsequent transformations using hydrazinolysis reactions, nucleophilic addition of phenylisothiocyanate and intramolecular alkaline heterocyclization. A number of S-derivatives of the obtained 4-phenyl-5-((5-phenylamino-1,3,4-thiadiazole-2-ylthio)methyl)-1,2,4-triazole-3-thione were synthesized by the interaction with haloalkanes in the presence of an equivalent amount of alkali in alcoholic medium. The structure of the obtained compounds was confirmed by elemental analysis, 1H NMR spectroscopy, and IR-spectrophotometry. The individuality of substances was established by high performance liquid chromatography. For the synthesized substances, an individual calculated screening was performed using the PASS Online® software product.Results. The procedure for preparing 4-phenyl-5-((5-phenylamino-1,3,4-thiadiazole-2-ylthio)methyl)-1,2,4-triazole-3-thione was optimized. The optimal synthesis conditions were determined S-alkylderivatives of 4-phenyl-5-((5-phenylamino-1,3,4-thiadiazole-2-ylthio)methyl)-1,2,4-triazole-3-thiol, the structure was established the obtained substances and their physical properties were studied. With the help of computer-assisted prediction Pass Online®, a promising direction for further studies of the biological activity of the target reaction products was determined.Conclusions. A series of S-alkylderivatives of 4-phenyl-5-((5-phenylamino-1,3,4-thiadiazole-2-ylthio)methyl)-1,2,4-triazole-3-thione were obtained, the structure of these compounds was confirmed by physical-chemical methods of analysis. At the next stages of the study, it would be planned to establish indicators of the antimicrobial activity of the synthesized substances. 

References

Asif, M. (2016). A review on pharmacological potentials of various substituted thiadiazole analogs. International Journal of Current Research in Applied Chemistry & Chemical Engineering, 2(2), 1-26.

Küçükgüzel, Ş., & Çıkla-Süzgün, P. (2015). Recent advances bioactive 1,2,4-triazole-3-thiones. European Journal Of Medicinal Chemistry, 97, 830-870. doi: 10.1016/j.ejmech.2014.11.033

Odyntsova, V. M., & Pruglo Ye. S. (2015). Synthesis, physical-chemical properties and the study of anti-hypoxemic activity of 5-(adamantane-1-yl)-4-R-1,2,4-triazole-3-thion alkylderivatives. Zaporozhye medical journal, 2(89), 93-96. doi: https://doi.org/10.14739/2310-1210.2015.2.42123

Saidov, N., Kadamov, I., Georgiyants, V., & Taran, A. (2014). Planning, Synthesis, and Pharmacological Activity of Alkyl Derivatives of 3-Mercapto-4-Phenyl-5-Arylaminomethyl-1,2,4-Triazole-(4H). Pharmaceutical Chemistry Journal, 47(11), 581-585. doi: 10.1007/s11094-014-1011-0

Sayed, S., Khalil, M., & Raslan, M. (2014). Synthesis of pyrazole, 1,3-dithiolan and thiophene derivatives pendant to thiazolo[2,3-c]-1,2,4-triazole moiety. European Journal Of Chemistry, 5(2), 356-362. doi: 10.5155/eurjchem.5.2.356-362.1022

Szulczyk, D., Tomaszewski, P., Jóźwiak, M., Kozioł, A., Lis, T., & Collu, D. et al. (2017). Synthesis and Biological Activities of Ethyl 2-(2-pyridylacetate) Derivatives Containing Thiourea, 1,2,4-triazole, Thiadiazole and Oxadiazole Moieties. Molecules, 22(3), 409. doi: 10.3390/molecules22030409

Pruhlo, Ye. S. (2016). Aktoprotektorna aktyvnist 5-(2-bromfenil)-4-amino-4N-1,2,4-triazol-3-tionu ta yoho S-pokhidnykh [Actoprotective activity of 5-(2-bromophenyl)-4-amino-4H-1,2,4-triazole-3-thione and its S-derivatives]. Current issues in pharmacy and medicine: science and practice, 1(20), 67-70. doi: 10.14739/2409-2932.2016.1.61438 [in Ukrainian].

Rud, A. M., Kaplaushenko, A. H., & Sameliuk, Yu. H. (2018). Syntez novykh alkilsulfonil(sulfinil) pokhidnykh 1,2,4-triazolu na osnovi (3-(alkiltio)-4-R-1,2,4-triazol-5-il)(fenil)metanoliv [Synthesis of new alkylsulfonyl(Sulfinyl)-1,2,4-triazole derivatives based on (3-(Alkylthio)-4-R-1,2,4-thriazole-5-yl)(phenyl)methanol’s]. Current issues in pharmacy and medicine: science and practice, 11(1), 23-28. doi: 10.14739/2409-2932.2018.1.123641 [in Ukrainian].

Suhak, O. A., Panasenko, O. I., & Knysh, Ye. H. (2017). Syntez, fizyko-khimichni vlastyvosti pokhidnykh 2-((4-R-5-(tiofen2-ilmetyl)-4H-1,2,4-triazol-3-il)tio)atsetohidrazydiv [Synthesis, physical-chemical properties of 2-((4-R-5-(thiophene-2-ylmethyl)-4H-1,2,4-triazole-3-yl)thio)acetohydrazides]. Current issues in pharmacy and medicine: science and practice, 11(1), 20-25. doi: 10.14739/2409-2932.2017.1.93432 [in Ukrainian].

Downloads

How to Cite

1.
Hotsulia AS, Fedotov SO. Synthesis and properties of some S-derivatives of 4-phenyl-5-((5-phenylamino-1,3,4-thiadiazole-2-ylthio)methyl)-1,2,4-triazole-3-thione. Current issues in pharmacy and medicine: science and practice [Internet]. 2019Nov.21 [cited 2024Jul.16];(3). Available from: http://pharmed.zsmu.edu.ua/article/view/184170

Issue

Section

Original research