Synthesis, physical-chemical properties and research of acute toxicity of 1,2,4-triazole derivatives containing thiophene core
DOI:
https://doi.org/10.14739/2409-2932.2015.3.52616Keywords:
1, 2, 4-triazole, Thiophene, Esthers, Acute Toxicity TestsAbstract
The aim of research. Modern drugs must have certain characteristics, such as low toxicity and high efficiency. Special attention should be given to esthers of 2-(1,2,4-triazoles-3-iltio)acetic acids. It has been found that compounds of this class are able to show analgesic, neuroleptic, diuretic, anti-inflammatory, mild antimicrobial and other biological activities and also can be intermediates for the synthesis of amides, hydrazides, ilidenhidrazides and bicyclic structures.
Therefore, we synthesized a series of esthers of 2-(4-R-5- (thiophene-2-yl)-4H-1,2,4-triazoles-3-iltio)acetic acids, to explore their physical and chemical properties, to explore the acute toxicity of the obtained compounds, to identify the nature and severity of their damaging effects on the body of experimental animals.
Materials and methods. Esthers of 2-((4-R-5-(thiophene-2-yl)-4H-1,2,4-triazol-3-yl)thio)acetic acids have been obtained by the etherification of the corresponding 2-((4-R-5-(thiophene-2-yl)-4H-1,2,4-triazol-3-yl)thio)acetic acids with methyl, ethyl, isopropyl and butyl alcohols in the presence of the catalytic amount of concentrated sulfuric acid.
The tabular rapid method of V. B. Prozorovskiy which was used in a number of scientists practical research, has been selected for the acute toxicity study. Test compounds were introduced intraperitoneally in doses from the logarithmic scale.
Results. 16 new derivatives of 2-((4-R-5-(thiophene-2-yl)-4H-1,2,4-triazoles-3-yl)thio)acetic acids have been synthesized. Physical-chemical constants have been checked for all synthesized compounds and their structure has been confirmed by using elemental analysis, 1H NMR- and IR-spectroscopy.
The indicators of acute toxicity have been studied for all synthesized compounds. The acute toxicity study of the esters of 2-((4-R-5-(thiophene-2-yl)-4H-1,2,4-triazoles-3-yl)thio)acetic acid shows that all compounds belong to the 4th or 5th grade of toxicity, they are practically non-toxic and low-toxic and their LD50 is in the range of 525±51 mg/kg to 2250±200 mg/kg.
References
Bihdan O.A. (2015) Syntez, fizyko-khimichni ta biolohichni vlastyvosti pokhidnykh 1,2,4-triazol-3-tioniv, yaki mistiat ftorfenilni zamisnyky (Dis…kand. farm. nauk). [Synthesis, physico-chemical and biological properties of derivatives of 1,2,4-triazoles-3-thiones containing substituents ftorfenilni. Dr. farm. sci. diss.]. Zaporizhzhia. [in Ukrainian].
Kazicyna, L. A. (1979) Primenenie UF-, IK-, YAMR- i MASS-spektroskopii v organicheskoj khimii [Application of UV, IR, NMR and mass spectrometry in organic chemistry]. Moscow. [in Russian].
Knysh, E. G. (1987) Sintez, fiziko-khimicheskie i biologicheskie svojstva N- i S-zameschennykh 1,2,4-triazola (Dis… dokt. farm. nauk). [Synthesis, physico-chemical and biological properties of N- and S-substituted 1,2,4-triazole Dr. farm. sci. diss.]. Zaporizhzhia. [in Ukrainian].
Panasenko, O. I. (2005) Syntez, peretvorennia, fizyko-khimichni ta biolohichni vlastyvosti amino- i tiopokhidnykh 1,2,4-triazolu (Dis… dokt. farm. nauk). [Synthesis, transformation, physico-chemical and biological properties amino and thioderivatives 1,2,4-triazoles. Dr. farm. sci. diss.]. Zaporizhzhia. [in Ukrainian].
Parchenko, V. V. (2014) Syntez, peretvorennia, fizyko-khimichni ta biolohichni vlastyvosti v riadi 5-furylzamishchenykh 1,2,4-triazol-3-tioniv (Dis… dokt. farm. nauk). [Synthesis, transformation, physico-chemical and biological properties of a number of 5-1,2,4-triazoles furylzamischenyh-3-thiones. Dr. farm. sci. diss.]. Zaporizhzhia. [in Ukrainian].
Klen, E. E′., Nikitina, I. L., Ivanova, O. A., Gabidullin, R. A., Agzamova, L. F., Alehin, E. K., & Haliullin, F. A. (2008) Sintez i antidepressivnaya aktivnost' e′firov 2-(3-brom-1,2,4-triazolil-5-tio)uksusnyh kislot, soderzhaschikh tietanovyj cikl [Synthesis and antidepressant activity of 2-(3-bromo-1,2,4-triazol-5-ylthio)acetic acid containing tietanovy cycle]. Bashkirskij khimicheskij zhurnal, 4, 21–22. [in Russian].
Sameliuk, Yu. H., & Kaplaushenko, A. G. (2013) Syntez, fizyko-khimichni ta biolohichni vlastyvosti 2-(5-(meto-ksyfenil)-1,2,4-triazol-3-tio)atsetatnykh kyslot ta yikh esteriv [Synthesis, physico-chemical and biological properties of 2- (5- (purpose-ksyfenil) -1,2,4-triazoles 3-thio) acetic acid and their esters]. Aktualni pytannia farmatsevtychnoi ta medychnoi nauky ta praktyky, 2, 125–128. [in Ukrainian].
Hotsulia, A. S., Panasenko, O. I., Knysh, Ye. H., & Pruhlo, Ye. S. (2010) Syntez, fizyko-khimichni vlastyvosti ta hostra toksychnist 2-[5-R-4-(2-metoksyfenil)-1,2,4-triazol-3-iltio]-1-aryletanoliv [Synthesis, physico-chemical properties and acute toxicity 2-[5-R-4-(2-methoxyphenyl)-1,2,4-triazoles 3-iltio]-1-aryletanole]. Farmatsevtychnyi zhurnal, 6, 32–35. [in Ukrainian].
Salionov, V. O., Panasenko, O. I., & Knysh, Ye. H. (2012) Syntez, fizyko-khimichni vlastyvosti 2-(4-R-5-(tiofen-2-il)-4N-1,2,4-triazol-3-iltio)atsetatnykh kyslot ta yikh solei [Synthesis, physico-chemical properties of 2-(4-R-5-(thiophene-2-yl)-4H-1,2,4-triazol-3-iltio)acetic acid and its salts]. Ukrainskyi biofarmatsevtychnyi zhurnal, 5-6, 114–117. [in Ukrainian].
Shcherbyna, R. O. (2014) Analiz farmakolohichnoi aktyvnosti pokhidnykh 1,2,4-triazolu [Analysis of pharmacological activity of derivatives of 1,2,4-triazoles]. Farmatsevtychnyi chasopys, 4, 145–150. [in Ukrainian].
Downloads
How to Cite
Issue
Section
License
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access)