Synthesis and Antibacterial Activity of Aromatic Diacetates

Muhammadu Isiyaku (1) , Yusuf Hassan (1) , Bashir Abdulkadir (2) , Yusuf Yilmaz (3)
(1) Department of Chemistry, Umaru Musa Yar’adua University, Katsina, Nigeria,
(2) Department of Microbiology, Umaru Musa Yar’adua University, Katsina, Nigeria,
(3) Department of Chemistry Technology, Naci Topçuoğlu Vocational School, Gaziantep University, 27310, Gaziantep, Türkiye

Abstract

The need to discover new generation of antibiotics with novel mechanism of action has continued to be of paramount importance due to the growing cases of resistant strains of bacterial species. In this work, some known aromatic diacetates were synthesised and characterised using NMR and FTIR spectroscopic techniques. The obtained compounds were subjected to in vitro susceptibility test using a disc diffusion method, and the minimum inhibitory concentration (MIC) of the compounds was also evaluated. Further testing for minimum bactericidal concentration (MBC) for the active compounds was also carried out. The susceptibility test recorded in comparison with a standard drug (ciprofloxacin) showed that all the compounds exhibited high activities against the organisms at 1,000 µg/ml except compound 2d which had no activity on Bacillus megaterium. The highest zone of inhibition of Staphylococcus aureus, Bacillus subtilitis, Bacillus megaterium, Pseudomonas aeruginosa, Escherichia coli, and Salmonella typhimurium were found to be 34 mm, 24 mm, 25 mm, 36 mm, 28 mm, 36 mm respectively. While, the lowest MIC and MBC values of 15 µg/ml were found for some of the compounds against some of the bacterial species.

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References

[1] WHO. (2023). Antimicrobial Resistance Fact Sheet. World Health Organization. Retrieved 1 July from https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance

[2] Samoori, N., Foroughifar, N., Khajeh-Amiri, A., & Pasdar, H. (2025). Synthesis, antimicrobial activity, and molecular docking study of 1, 3-oxazines derivatives. Int. J. Ind. Chem., 16(1).

[3] Huang, H., Zhang, Y., Du, Q., Zheng, C., Jin, C., & Li, S. (2024). Synthesis and Antimicrobial Activity of 3-Alkylidene-2-Indolone Derivatives. Molecules, 29(22), 5384.

[4] Argentin, M.N., Cruz, F.D.P.N., Souza, A.B., D’Aurea, E.M.D.O., Bastos, J.K., Ambrósio, S.R., Veneziani, R.C.S., Camargo, I.L.B.C. & Mizuno, C.S. (2023). Synthesis and antibacterial activity of polyalthic acid analogs. Antibiotics, 12(7), 1202.

[5] Zain El-Dein, A. M., Abdel Aleem, A. A. H., & El-Sayed, I. E. (2023). Synthesis and Antibacterial Activity of Some Novel Quinoline Analogues. Egypt J. Chem., 66(6), 323-330.

[6] Gul, M., Turk Celikoglu, E., Idil, O., Tas, G., & Pelit, E. (2023). Synthesis, antimicrobial activity and molecular docking studies of spiroquinoline-indoline-dione and spiropyrazolo-indoline-dione derivatives. Sci. Rep., 13(1), 1676.

[7] Nirwan, N., Pareek, C., Chohadia, A. K., & Verma, K. K. (2023). Synthesis, antibacterial, and antifungal activities of 3-(4, 5-Diphenyl-1H-imidazol-2-yl)-1H-Indole derivatives. J. Sci. Res., 15(1), 159-170.

[8] Kartsev, V., Geronikaki, A., Zubenko, A., Petrou, A., Ivanov, M., Glamočlija, J., Sokovic, M., Divaeva, L., Morkovnik, A. & Klimenko, A. (2022). Synthesis and antimicrobial activity of new heteroaryl (aryl) thiazole derivatives molecular docking studies. Antibiotics, 11(10),1337.

[9] Palabindela, R., Myadaravenia, P., Banothu, D., Korra, R., Mekala, H., & Kasula, M. (2022). Anthracene and 1, 8-napthalimide aminothiazole hybrids: Synthesis, Antimicrobial activity and Molecular Docking Studies. Orient. J. Chem., 38(1), 137.

[10] Bayram, G., Nzeyımana, A., Utku, S., Ülger, M., Aslan, G., &

Berçın, E. (2012). Study on synthesis and antimicrobial activities of some michael-type addition compounds. JFPAU, 45(2), 182-193.

[11] Evrard, A., Siomenan, C., Etienne, C. T., Daouda, T., Souleymane, C., Drissa, S., & Ané, A. (2021). Design, synthesis and in vitro antibacterial activity of 2-thiomethyl-benzimidazole derivatives. Adv. Biol. Chem., 11(4), 165-177.

[12] El Malah, T., Nour, H. F., Satti, A. A., Hemdan, B. A., & El-Sayed, W. A. (2020). Design, synthesis, and antimicrobial activities of 1, 2, 3-triazole glycoside clickamers. Molecules, 25(4), 790.

[13] Jin, Q. H., Fu, Z. Y., Xia, Y. N., Liu, B. Y., & Jiang, H. Y. (2020). Synthesis and antibacterial activity of a series novel 5, 7-diisoprenyloxyflavone derivatives. Braz. J. Pharm. Sci., 56, e17721.

[14] Al-Omar, M. A. (2010). Synthesis and antimicrobial activity of new 5-(2-thienyl)-1, 2, 4-triazoles and 5-(2-thienyl)-1, 3, 4-oxadiazoles and related derivatives. Molecules, 15(1), 502-514.

[15] Sahu, J. K., Ganguly, S., & Kaushik, A. (2014). Synthesis and antimicrobial activity of some novel fused heterocyclic 1, 2, 4-triazolo [3, 4-b][1, 3, 4] thiadiazine derivatives. J. Adv. Pharm. Technol. Res. 5(2), 90-95.

[16] Yalcin, I., Tekiner, P. E. R. V. İ. N., Oren, İ. L. K. A. Y., Arpaci, Ö. Z. L. E. M., Aki-Sener, E., & Altanlar, N. (2003). Synthesis and antimicrobial activity of some novel 2, 6, 7-trisubstituted-2H-3, 4-dihydro-1, 4-benzoxazin-3-one derivatives. Indian J. Chem., Sect. B., 42(4).

[17] El Faydy, M., Dahaieh, N., Ounine, K., Rastija, V., Almalki, F., Jamalis, J., ... & Lakhrissi, B. (2021). Synthesis and antimicrobial activity evaluation of some new 7-substituted quinolin-8-ol derivatives: POM analyses, docking, and identification of antibacterial pharmacophore sites. CDC, 31, 100593.

[18] Nasr, A. Z., Farahat, A., Zein, M. A., & Abdelrehim, E. S. M. (2022). Synthesis and Antimicrobial Activity of 1, 3, 4-Oxadiazoline, 1, 3-Thiazolidine, and 1, 2, 4-Triazoline Double-Tailed Acyclo C-Nucleosides. ACS omega, 7(20), 16884-16894.

[19] Fadel, Z., & Al-Azzawi, A. M. (2021). Design, synthesis and antimicrobial activity evaluation of new bisimidyl sulfonamido ketone comprising drug component. Chem. Methodol., 5(6): 464-70.

[20] Rezk, M. M., Wasfy, A. A. F., Behalo, M. S., El-kalyoubi, S., & Aly, A. A. (2025). Synthesis, Antimicrobial Activity and Molecular Docking of Novel Series of Phthalazine Derivatives. Egypt. J. Chem., 68(13), 289-306.

[21] Youns, N. M. (2024). Synthesis, characterization and antimicrobial activity of new 4-aminoantipyrine derivatives using ultrasonic mediation. Baghdad Sci. J., 21(9), 4.

[22] Bukhari, S. N. A., Abdelgawad, M. A., Ahmed, N., Amjad, M. W., Hussain, M. A., Elsherif, M. A., ... & Janković, N. (2023). Synthesis, Characterization, and Biological Evaluation of Meldrum’s Acid Derivatives: Dual Activity and Molecular Docking Study. Pharmaceuticals, 16(2), 281.

[23] Pourmousavi, S. A., & Zinati, Z. (2009). H2(SO)4-silica as an efficient and chemoselective catalyst for the synthesis of acylal from aldehydes under solvent-free conditions. Turk. J. Chem., 33(3), 385-392.

Authors

Muhammadu Isiyaku
[email protected] (Primary Contact)
Yusuf Hassan
Bashir Abdulkadir
Yusuf Yilmaz
Synthesis and Antibacterial Activity of Aromatic Diacetates. (2026). Journal of Pure & Applied Sciences , 25(1), 87-91. https://doi.org/10.51984/yvp0kb93

Article Details

How to Cite

Synthesis and Antibacterial Activity of Aromatic Diacetates. (2026). Journal of Pure & Applied Sciences , 25(1), 87-91. https://doi.org/10.51984/yvp0kb93

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