Microwave-assisted, [Bmim]HSO4-catalyzed synthesis of tetrasubstituted imidazoles via four-component reaction

Dau Xuan Duc, Ho Thi Lanh
Author affiliations

Authors

  • Dau Xuan Duc School of Chemistry, Vinh University, 182 Le Duan Street, Vinh City, Viet Nam
  • Ho Thi Lanh School of Chemistry, Vinh University, 182 Le Duan Street, Vinh City, Viet Nam

DOI:

https://doi.org/10.15625/2525-2518/16492

Keywords:

Ionic liquid, Debus–Radziszewski reaction, aryl aldehyde, substituted imidazole

Abstract

Imidazole derivatives are one of the most important classes of nitrogen-containing five-membered heterocycles with a wide range of biological activities. Thus, the synthesis of these heterocycles has attracted intensive research interest. The classical Debus–Radziszewski reaction is one of the most facile and straightforward methods to synthesize 2,4,5-trisubstituted imidazoles and 1,2,4,5-tetrasubstituted imidazoles. Various catalysts have been developed for this synthesis to improve efficiency and reduce environmental pollution. Ionic liquids, green solvents for synthesis, have also been employed for this synthesis. Furthermore,  the use of microwave irradiation, which can bring many advantages such as: high yield of products, simple work-up, improved selectivity, and clean reaction pathways, has also investigated for this method. Herein, we described the synthesis of tetrasubstituted imidazoles under microwave irradiation. The four-component reaction of benzil, aryl aldehyde, ammonium acetate, and primary amine was performed using ionic liquid [Bmim]HSO4 as the catalyst. Ten imidazole derivatives were furnished in high yield using an environmentally benign procedure. All of products were formed in a short time and simply purified by filtration and crystallization. Structures of all synthesized compounds were characterized by 1H and 13C NMR data analysis and by comparison with reported data. Interestingly, some synthesized compounds have been reported to possess antifungal activity on some fungi.

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References

Alghamdi S. S., Suliman R. S., Almutairi K., Kahtani K., and Aljatli D. - Imidazole as a promising medicinal scaffold: current status and future direction, Drug Des. Devel. Ther. (2013) 3289-3312.https://doi.org/10.2147/DDDT.S307113.

Shahoo U., Biswal S., Sethy S., Kumar H. S. K., and Banerjee M. - Imidazole and its biological activities: A review, Asian J. Res. Chem. 5 (2012) 171-182. https://doi.org/10.5958/0974-4150.

Lee S. G. - Functionalized imidazolium salts for task-specific ionic liquids and their applications, Chem. Commun. (2006) 1049-1063.https://doi.org/10.1039/B514140K

Tomizaki K. Y., Shimizu S., Onoda M., and Fujioka Y. - An acid dissociation constant (pKa)-based screening of chemical absorbents that preferably capture and release pressurized carbon dioxide for greenhouse gas control, Chem. Lett. 37 (2008) 516-517. https://doi.org/10.1246/cl.2008.516.

Abhishek P., Kulkarni C. J., Tonzola A. B.,and Samson A. J. - Electron transport materials for organic light-emitting diodes, Chem. Mater. 16 (2004) 4556-4573. https://doi.org/10.1021/cm049473l.

Wang Z., Lu P., Chen S., Gao Z., Shen F., Zhang W., Xu Y., Kwok H. S., and Ma Y. J. - Phenanthro[9,10-d]imidazole as a new building block for blue light emitting materials, Mater. Chem. 21 (2011) 5451-5456. https://doi.org/10.1039/C1JM10321K.

Bhalla R., Helliwell M., and Garner C. D. - Synthesis and coordination chemistry of the bis(imidazole) ligand, bis(1-methyl-4,5-diphenylimidaz-2-oyl)(benzyloxy)methane, Inorg. Chem. 36 (1997) 2944-2949. https://doi.org/10.1021/ic961204c.

Zhou L., and Nicholas K. M. - Imidazole substituent effects on the oxidative reactivity of tripodal (imid)2(thioether)CuI complexes, Inorg. Chem. 47 (2008) 4356-4367. https://doi.org/10.1021/ic800007t.

Bourissou D., Guerret O., Gabbai F. P., and Bertrand G. - Stable carbenes, Chem. Rev. 100 (2000) 39-92. https://doi.org/10.1021/cr940472u.

Debus Heinrich. - Ueber die einwirkung des ammoniaks auf glyoxal, Justus Liebigs Ann. Chem. 107 (1858) 199-208. doi:10.1002/jlac.18581070209.

Radzisewski Br. - Ueber glyoxalin und seine homologe, Chem. Ber. 15 (1882) 2706-2708. doi:10.1002/cber.18820150224.

Kerru N., Bhaskaruni S. V. H. S., Gummidi L., Maddila S. L., Maddila, S., Jonnalagadda S. B. - Recent advances in heterogeneous catalysts for the synthesis of imidazole derivatives, Synth. Commun. 49 (2019) 2437-2459. https://doi.org/10.1080 /00397911.2019.1639755

Shabalin D. A., and Camp J. E. - Recent advances in the synthesis of imidazoles, Org. Biomol. Chem. 18 (2020) 3950-3964.https://doi.org/10.1039/D0OB00350F.

Davoodnia A., Heravi M. M., Safavi-Rad Z., and Tavakoli-Hoseini N. - Green, one-pot, solvent-free synthesis of 1,2,4,5-tetrasubstituted imidazoles using a Brønsted acidic ionic liquid as novel and reusable catalyst, Synth. Commun. 40 (2010) 2588-2597. https://doi.org/10.1080/00397910903289271.

Bougrin K., Loupy A., and Soufiaoui M. - Microwave-assisted solvent-free heterocyclic synthesis, J. Photochem. Photobiol. C: Photochem. Rev. 6 (2005) 139-167. https://doi.org/10.1016/j.jphotochemrev.2005.07.001.

Shekarchi M., and Behbahani F. K. - [Bmim]HSO4-catalyzed synthesis of tetrasubstituted imidazoles as potential mutant isocitrate dehydrogenase 1 inhibitors, Russian J. Org. Chem. 56 (2020). https://doi.org/894-900. 10.1134/S1070428020050243.

Wang D., Li Z., Huang X., and Li Y. - Ce(SO2)2•4H2O as a highly efficient catalyst for the one–pot synthesis of tri- and tetra–substituted imidazoles under solvent–free conditions, ChemistrySelect 4 (2016) 664-668. https://doi.org/10.1002/slct.201600029.

Vargas J. A. R., Lopez A. G., Perez Y., Cos P. and Froeyen M. - In vitro evaluation of arylsubstituted imidazoles derivatives as antiprotozoal agents and docking studies on sterol 14α-demethylase (CYP51) from Trypanosoma cruzi, Leishmania infantum, and Trypanosoma brucei, Parasitol. Res. 118 (2019) 1533-1548. https://doi.org/10.1007/s00436-019-06206-z.

Kumar D., Kommi D. N., Patel A. R., and Chakraborti A. K. - Catalytic procedures for multicomponent synthesis of imidazoles: selectivity control during the competitive formation of tri- and tetrasubstituted imidazoles, Green Chem. 14 (2012), 2038-2049. https://doi.org/10.1039/C2GC35277J.

Zhang F., Gao Q., Chen B., Bai Y., Sun W., Lv D., and Ge M. - A practical and green approach towards synthesis of multi-substituted imidazoles using boric acid as efficient catalyst, Phosphorus Sulfur Silicon Relat, Elem. 191 (2016) 186-189. https://doi.org/10.1080/10426507.2015.1100184.

Mahdavinia G. H., Amani A, M., and Sepehrian H. - MCM-41-SO3H as a highly efficient sulfonic acid nanoreactor for the rapid and green synthesis of some novel highly substituted imidazoles under solvent-free condition, Chin. J. Chem. 30 (2012) 703-708. https://doi.org/10.1002/cjoc.201280008.

Bansal R., Soni P. K., and Halve A. K. Green synthesis of 1,2,4,5-tetrasubstituted and 2,4,5-trisubstituted imidazole derivatives involving one-pot multicomponent reaction. J. Heterocyclic Chem. 55 (2018) 1308-1312. https://doi.org/10.1002/jhet.3160.

Zhang F., Gao, Q., Chen B., Bai I., Sun W., Lv D., and Ge M. - A Practical and Green Approach towards Synthesis of Multi-substituted Imidazoles Using Boric acid as Efficient Catalyst, Phosphorus Sulfur Silicon Relat. Elem. 191 (2016) 786-789. https://doi.org/10.1080/10426507.2015.1100184.

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Published

08-07-2022

How to Cite

[1]
D. X. Duc and H. T. Lanh, “Microwave-assisted, [Bmim]HSO4-catalyzed synthesis of tetrasubstituted imidazoles via four-component reaction”, Vietnam J. Sci. Technol., vol. 60, no. 3, pp. 383–390, Jul. 2022.

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Natural Products