Synthesis and the Antimicrobial Activity of Salt Carbenoid Compounds
DOI:
https://doi.org/10.24959/ophcj.22.258880Keywords:
fluoroaryl, cetyl-, 1-adamantyl substituted heterocyclic salts, antimicrobial activityAbstract
Aim. To synthesize aliphatic and aromatic derivatives of salt carbenoid compounds of the series of imidazole, benzimidazole, pyridine, pyrimidine and 1,3,4-oxadiazole containing fluorophenyl, cetyl or adamantyl substituents, and study their antimicrobial (antibacterial and antifungal) activities.
Results and discussion. New derivatives of heterocyclic carbenoid salts and zwitterions based on the imidazole, benzimidazole, pyridine, pyrimidine and 1,3,4-oxadiazole heterocyclic systems containing fluorophenyl, cetyl or adamantyl substituents were synthesized. For this purpose, reactions of cyclization of the corresponding diimines with ethoxymethyl chloride (imidazolium salts), quaternization of the corresponding azoles with cetyl bromide or 1-adamantyl bromide in organic solvents (benzimidazolium, pyridinium and 1,3,4-oxadiazolium salts), cyclization of di(1-adamantylamino)alkanes hydrobromides with the orthoformic ester (4,5-dihydroimidazolium and tetrahydropyridinium salts) were used. Zwitterionic compounds were obtained by the reaction of the corresponding azolium salts with phenyl isothiocyanate in the presence of potassium carbonate. Some macrocyclic and adamantyl substituted heterocyclic compounds showed antifungal and antibacterial activities.
Experimental part. The structure of the compounds synthesized was proven by 1H and 13C NMR spectroscopy methods. The antimicrobial activity was studied out by the agar diffusion method to determine diameters of the growth inhibition zones of microorganisms (bacteria and fungi) and by the method of serial dilutions to determine the minimum inhibitory concentration and minimum bactericidal and fungicidal concentrations.
Conclusions. The synthesis of new heterocyclic carbenoid salts and zwitterions based on the imidazole, benzimidazole, pyridine, pyrimidine and 1,3,4-oxadiazole heterocyclic systems containing fluorophenyl, cetyl or adamantyl substituents has been performed. Compounds of macrocyclic and adamantyl heterocyclic series with antifungal and antibacterial activities have been found. 1,3-Dicetylimidazolium bromide, macrocyclic bis(decylenebenzimidazolium) bromides, azolium-N-phenylthiocarboximides have been proven to be the most active.
Supporting Agency
- A grant of the National Academy of Sciences of Ukraine No. II-01-22
Downloads
References
- Gravel, J.; Schmitzer, A. R. Imidazolium and benzimidazolium-containing compounds: from simple toxic salts to highly bioactive drugs. Org. Biomol. Chem. 2017, 15 (5), 1051-1071. https://doi.org/10.1039/C6OB02293F.
- Pernak, J.; Sobaszkiewicz, K.; Mirska, I. Anti-microbial activities of ionic liquids. Green Chem. 2003, 5 (1), 52-56. https://doi.org/10.1039/B207543C.
- Garcia, M. T.; Ribosa, I.; Perez, L.; Manresa, A.; Comelles, F. Aggregation Behavior and Antimicrobial Activity of Ester-Functionalized Imidazolium- and Pyridinium-Based Ionic Liquids in Aqueous Solution. Langmuir 2013, 29 (8), 2536-2545. https://doi.org/10.1021/la304752e.
- Cancemi, P.; Buttacavoli, M.; D'Anna, F.; Feo, S.; Fontana, R. M.; Noto, R.; Sutera, A.; Vitale, P.; Gallo, G. The effects of structural changes on the anti-microbial and anti-proliferative activities of diimidazolium salts. New J. Chem. 2017, 41 (9), 3574-3585. https://doi.org/10.1039/C6NJ03904A.
- Achar, G.; Agarwal, P.; Brinda, K. N.; Małecki, J. G.; Keri, R. S.; Budagumpi, S. Ether and coumarin–functionalized (benz)imidazolium salts and their silver(I)–N–heterocyclic carbene complexes: Synthesis, characterization, crystal structures and antimicrobial studies. J. Organomet. Chem. 2018, 854, 64-75. https://doi.org/10.1016/j.jorganchem.2017.11.005.
- Turkyilmaz, M.; Uluçam, G.; Aktaş, Ş.; Okan, S. E. Synthesis and characterization of new N-heterocyclic carbene ligands: 1,3-Bis(acetamide)imidazol-3-ium bromide and 3-(acetamide)-1-(3-aminopropyl)-1H-imidazol-3-ium bromide. J. Mol. Struct. 2017, 1136, 263-270. https://doi.org/10.1016/j.molstruc.2017.02.022.
- Liu, L.; Huang, Y.; Riduan, S. N.; Gao, S.; Yang, Y.; Fan, W.; Zhang, Y. Main-chain imidazolium oligomer material as a selective biomimetic antimicrobial agent. Biomaterials 2012, 33 (33), 8625-8631. https://doi.org/10.1016/j.biomaterials.2012.08.006.
- Korotkikh, N. I.; Shvaika, O. P.; Kiselyov, A. V.; Knishevitsky, A. V.; Glinyana, N. V.; Marichev, K. A.; Novikov, V. P.; Lubenets, V. I.; Iskiv, O. P.; Moskalenko, N. I.; Komarovska-Porokhnyavets, O. Z. Antymikrobna aktyvnist proto- ta metalo-karbenovykh spoluk riadu azoliv ta azyniv [Antimicrobial activity of proto- and metal-carbene compounds of the azole and azine series, in Ukrainian]. Visnyk Natsionalnoho universytetu “Lvivska politekhnika” 2008, 622, 3–6.
- Kiselyov, A. V.; Knishevitsky, A. V.; Rayenko, G. F.; Korotkikh, N. I.; Pekhtereva, T. M.; Shvaika, O. P.; Klimnyuk, S. I.; Pokryshko, O. V.; Gryschuk, B. D. Synthesis and antimicrobial activity of some aromatic derivatives of azoles. Journal of Organic and Pharmaceutical Chemistry 2009, 7 (1), 59–63.
- Marichev, K. A.; Glinyana, N. V.; Korotkikh, N. I.; Shvaika, O. P.; Kiselyov, A. V.; Knishevitsky, A. V.; Dudarenko, G. V.; Komarovska-Porokhnyavets, O. Z. Novikov, V. P.; Lubenets, V. I. Antimicrobial activity of proto- and metal-carbene compounds of azoles and pyridine. Journal of Organic and Pharmaceutical Chemistry 2011, 9 (3), 72–79.
- Marichev, K. O. Syntez i vlastyvosti novykh typiv karbenoidiv azolnoho riadu. Makrotsyklichni i polimerni systemy [Synthesis and properties of new types of azole carbenoids. Macrocyclic and polymer systems, in Ukrainian]. Ph.D. Thesis, L. M. Litvinenko Institute of Physical Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Donetsk, 2012.
- Saberov, V. Sh.; Marichev, K.A.; Korotkikh, N. I.; Shvaika, O. P.; Rodik, R.V.; Drapaylo, A.B.; Pekhtereva, T.M.; Komarovska-Porokhnyavets, O. Z.; Lubenets, V. I.; Novikov, V.P. Synthesis and antimicrobial activity of precarbene and metal-carbene compounds of the imidazole series. Journal of Organic and Pharmaceutical Chemistry 2014, 12 (2), 36–43. https://doi.org/10.24959/ophcj.14.790.
- 13. Glinyana, V.; Saberov, V. Sh.; Knishevitsky, A. V.; Korotkikh, N. I.; Shvaika, O. P.; Papayanina, O. S.; Komarovska-Porokhnyavets, O. Z.; Lubenets, V. I.; Novikov, V. P. Synthesis and antimicrobial activity of metal-carbene compounds of the 1,2,4-triazole series. Journal of Organic and Pharmaceutical Chemistry 2014, 12 (2), 44–52. https://doi.org/10.24959/ophcj.14.793.
- Korotkikh, N. I.; Rayenko, G. F.; Saberov, V. Sh.; Derevenets, M. О. 1-Adamantylzamishcheni tsyklichni formamidyniievi soli [1-Adamantyl substituted cyclic formamidinium salts, in Ukrainian]. Ukraine patent 141798, April 27, 2020.
- 15. Korotkikh, N. I.; Rayenko, G. F.; Saberov, V. Sh.; Derevenets, M. О. Sposib syntezu alifatychnykh pokhidnykh tsyklichnykh formamidyniievykh solei [Method for the preparation of aliphatic derivatives of cyclic formamidinium salts, in Ukrainian]. Ukraine patent 141799, April 27, 2020.
- 16. Glinyanaya, N. V.; Rayenko, G. F.; Korotkikh, N. I.; Rusanov, E. B.; Ryabitsky, A. B.; Shvaika, O. P. Halogen-containing heteroaromatic carbenes of the 1,2,4-triazole series and their transformations. RSC Adv. 2021, 11 (49), 30841-30848. https://doi.org/10.1039/D1RA04337D.
- 17. Pro zatverdzhennia metodychnykh vkazivok “Vyznachennia chutlyvosti mikroorhanizmiv do antybakterialnykh preparativ” [Guidlines “Determination of the susceptibility of microorganisms to antibacterial drugs”, in Ukrainian]. https://zakon.rada.gov.ua/rada/show/v0167282-07#Text (accessed February 11, 2022), Ministry of Health of Ukraine, Order #167, 05.04.2007.
- Harkavenko, Т. О.; Gorbatyuk, О. І.; Kozytska, T. G.; Andriyashchuk, V. O.; Harkavenko, V. M.; Dybkova, S. М.; Azirkin, І. В. Metodychni vkazivky shchodo vyznachennya chutlyvosti mikroorhanizmiv do antybakterial'nykh preparativ [Guidelines for determining the susceptibility of microorganisms to antimicrobial drugs, in Ukrainian]; State Scientific Research Institute of Laboratory Diagnostics and Veterinary and Sanitary Expertise: Kyiv, 2021.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2022 National University of Pharmacy
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors publishing their works in the Journal of Organic and Pharmaceutical Chemistry agree with the following terms:
1. Authors retain copyright and grant the journal the right of the first publication of the work under Creative Commons Attribution License allowing everyone to distribute and re-use the published material if proper citation of the original publication is given.
2. 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) providing proper citation of the original publication.
3. Authors are permitted and encouraged to post their work online (e.g. in institutional repositories or on authors’ personal websites) 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).