A review of benzotriazole derivatives: versatile scaffolds for advancing therapeutics in medicinal chemistry
Abstract
Benzotriazole (BtH) is recognized as a versatile heterocyclic scaffold that plays an increasingly vital role in modern drug discovery owing to its broad pharmacological potential and structural flexibility. Although BtH was first synthesized in the 19th century, recent advances in synthetic and medicinal chemistry have revitalized interest in BtH and its derivatives for developing multifunctional therapeutics. This review addresses current challenges and opportunities in BtH chemistry by integrating progress in sustainable synthesis, structure–activity relationship (SAR) analyses, and therapeutic applications. The discussion encompasses green methodologies, such as microwave-assisted, ultrasound-assisted, flow, and electrosynthesis techniques, that improve atom economy, reduce waste, and enhance energy efficiency. It also highlights how structural modifications, including halogenation, heterocyclic fusion, and metal complexation, influence biological activity and target selectivity. BtH derivatives exhibit significant antimicrobial, antiviral, anticancer, antioxidant, and enzyme-inhibitory properties, as well as other potential in neuroprotective and anti-inflammatory therapies. However, limited in vivo evaluation, lack of standardized bioassay protocols, and scalability challenges in sustainable synthesis remain key research gaps. Overall, this review synthesizes contemporary developments from 2020–2026, demonstrating that BtH serves as a privileged pharmacophore capable of engaging diverse biological targets. By consolidating mechanistic insights and eco-efficient synthesis strategies, the work provides a foundation for designing next-generation BtH-based drug candidates and advancing sustainable medicinal chemistry.
Keywords
Full Text:
PDFReferences
Bollikolla HB, Boddapati SNM, Thangamani S, Mutchu BR, Alam MM, Hussien M, Jonnalagadda SB. Advances in synthesis and biological activities of benzotriazole analogues: A micro review. J Heterocyclic Chem. 2022;60:705-742. doi:10.1002/jhet.4587
Gangurde KB, More RA, Adole VA, Ghotekar DS. Design, synthesis and biological evaluation of new series of benzotriazole-pyrazole clubbed thiazole hybrids as bioactive heterocycles: Antibacterial, antifungal, antioxidant, cytotoxicity study. J Mol Struct. 2024;1299:136760. doi:10.1016/j.molstruc.2023.136760
Kshatriya MR, Gajjar JA. Benzotriazole and its derivatives: A comprehensive review of its synthesis, activities and applications. Curr Chem Lett. 2025;14:299-322. doi:10.5267/j.ccl.2024.11.004
Verma K, Singh N. Microwave assisted synthesis of benzotriazole derivatives for anti-corrosive study on mild steel in acidic medium. J Phys Conf Ser. 2020;1531:012110. doi:10.1088/1742-6596/1531/1/012110
Alraqa SY, Alharbi K, Aljuhani A, Rezki N, Aouad MR, Ali I. Design, click conventional and microwave syntheses, DNA binding, docking and anticancer studies of benzotriazole-1,2,3-triazole molecular hybrids with different pharmacophores. J Mol Struct. 2021;1225:129192. doi:10.1016/j.molstruc.2020.129192
Feng J, Wang Q, Duan R, Li H, Zheng K, Wang X, Hie G. A facile electrosynthesis of N-acyl benzotriazoles from aldehydes and benzotriazole. Tetrahedron Lett. 2022;101:153904. doi:10.1016/j.tetlet.2022.153904
Liu H-F, Li Y, Wang G-A, Chen K-W, Tang H-T, Pan Y-M, He M-X, Yang K-D, Huang Y-L. Electrochemical Three-Component Reaction to Construct N-(α-alkoxyalkyl)benzotriazoles. Adv Synth Catal. 2023;365:3586-3590. doi:10.1002/adsc.202300593
Anjana VS, Kumar PM. An overview on medicinal perspective and biological behavior of benzotriazole; synthetic study on its multifaceted biological activities. IJRR. 2021;8:365-378. doi:10.52403/ijrr.20210546
Dandge A, Manikpuriya S, Sanap G. Benzotriazole derivatives and its pharmacological activity. Int J Pharm Sci. 2023;1:948-957. doi:10.5281/zenodo.10443937
Chaudhari NS, Khan MSAA, Khan MFAA, Azam SMOM, Nayak SSP. Investigating the antimicrobial activity of derivatives of benzotriazole. JRASB. 2024;3:1-6. doi:10.55544/jrasb.3.6.1
Malvade PV, Bhawar HS, Medge VA. Understanding the chemistry & pharmacology of benzotriazole in pharmaceutical applications. WJPR. 2025;14:289-314.
Rokde V, Danao K, Nimje J, Nandurkar D, Yerne T, Yadav P, Mahajan U. Design, synthesis, antimicrobial evaluation of novel 2-oxo-4-substituted aryl-azetidine benzotriazole derivatives. Chem Biodiversity. 2023;20:e202300433. doi:10.1002/cbdv.202300433
Mermer A, Bulbul MV, Kalender SM, Keskin I, Tuzun B, Eyupoglu OE. Benzotriazole-oxadiazole hybrid compounds: Synthesis, anticancer activity, molecular docking and ADME profiling studies. J Mol Liq. 2022;359:119264. doi:10.1016/j.molliq.2022.119264
Kleoff M, Boeser L, Baranyi L, Heretsch P. Scalable synthesis of benzotriazoles via [3+2] cycloaddition of azides and arynes in flow. Eur J Org Chem. 2021;2021:979-982. doi:10.1002/ejoc.202001543
Riley LM, Mclay TN, Sutherland A. Synthesis and fluorescent properties of alkynyl-and alkenyl-fused benzotriazole-derived α‑amino acids. J Org Chem. 2023;88:2453-2463. doi:10.1021/acs.joc.2c02886
Uesaka T, Ishitani T, Sawada R, Maeda T, Yagi S. Fluorescent 2-phenyl-2H-benzotriazole dyes with intramolecular N–H⋅⋅⋅N hydrogen bonding: Synthesis and modulation of fluorescence properties by proton-donating substituents. Dyes Pigm. 2020;183:108672. doi:10.1016/j.dyepig.2020.108672
Gu X-W, Zhao Y-H, Wu X-F. [3 + 2] Cycloaddition of azides with arynes formed via C–H deprotonation of aryl sulfonium salts. Green Chem. 2023;25:6282-6286. doi:10.1039/d3gc02052e
Yadav MS, Gupta A, Bose P, Singh AS, Mohapatra PP, Tiwari VK. Synthetic utility of N-acylbenzotriazoles. SynOpen. 2023;7:430-465. doi:10.1055/a-2157-5782
Galenko EE, Shakirova FM, Bodunov VA, Novikov MS, Khlebnikov AF. 1‐(2H‐Azirine‐2‐carbonyl)benzotri-azoles: building blocks for the synthesis of pyrrole‐containing heterocycles. Org Biomol Chem. 2020;18:2283-2296. doi:10.1039/D0OB00206B
Dasai PS, Parekh DV. Synthesis, characterization and biological screening of ligand 2-{[2-(5-benzoyl-1H-1,2,3-benzotriazole-1-yl)-2-oxoethyl]amino} propionic acid. Rasayan J Chem. 2021;14:959-966. doi:10.31788/RJC.2021.1426274
Dasai PS, Parekh DV. Synthesis, characterization and biological screening of novel metal(II) complexes of 2-{[2-(5-Benzoyl-1H-benzotriazol-1-yl)-2-oxoethyl]-amino}-5-bromobenzoic acid. Asian J Chem. 2021;33:747-751. doi:10.14233/ajchem.2021.23073
Pandey RK, Gupta M, Rajput CS, Singh AS. Synthesis of N-acyl-benzotriazole using Mukaiyama reagent. Arkivoc. 2023;vii:202312042. doi:10.24820/ark.5550190.p012.042
Menteşe E, Çalışkan N, Sökmen BB, Akyüz G. Synthesis and biological evaluation of coumarin-amino acid-benzotriazole conjugates. Russ J Bioorg Chem. 2024;50:191-200. doi:10.1134/S1068162024010126
Ling N, Wang X, Zeng D, Zhang Y-W, Fang X, Yang H-X. Synthesis, characterization and biological assay of three new benzotriazole-based Zn(II) complexes. J Mol Struct. 2020;1206:127641. doi:10.1016/j.molstruc.2019.127641
Murcia‑Galán RA, Durán SM, Leal‑Pinto SM, Roa‑Cordero MV, Vargas JD, Herrera LV, Muñoz‑Castro A, MacLeod‑Carey D, Naranjo TW, Rodríguez‑Kessler PL, Hurtado JJ. Antifungal activity of Co(II) and Cu(II) complexes containing 1,3‑bis(benzotriazol‑ 1‑yl)‑propan‑2‑ol on the growth and virulence traits of fluconazole‑resistant Candida species: synthesis, DFT calculations, and biological activity. BMC Chem. 2023;13:135. doi:10.1186/s13065-023-01037-7
Elzein A, Al Jomeh GAS, Tizzard GJ, Coles SJ, Banti, CN, Hadjikakou SK, Kostakis GE. Investigating the antimicrobial activity of 1-heteroaryl benzotriazole silver compounds. RSC Adv. 2025;15:11431-11440. doi:10.1039/d5ra01072a
Elagawany M, Maram L, Elgendy B. Novel synthesis of benzotriazolyl alkyl esters: an unprecedented CH2 insertion. RSC Adv. 2021;11:7564-7569. doi:10.1039/d0ra10413b
Vemuri PY, Patureau FW. Cross-dehydrogenative N−N coupling of aromatic and aliphatic methoxyamides with benzotriazoles. Org Lett. 2021;23:3902-3907. doi:10.1021/acs.orglett.1c01034
Kalari S, Karale UB, Rode HB. Selectfluor-mediated synthesis of β‑acyl allyl sulfones/β-acyl allyl benzotriazoles from ketones/acetylenes, aryl sulinates/ benzotriazole, and DMSO as a dual-carbon synthon. J Org Chem. 2022;87:2435-2445. doi:10.1021/acs.joc.1c02348
Tang Q, Li S-J, Ye X, Yuan T, Zhao K, He Y, Shan C, Wojtas L, Richardson D, Lan Y, Shi X. Design and synthesis of stable four-coordinated benzotriazole-borane with tunable fluorescence emission. Chem Sci. 2022;13:5982-5987. doi:10.1039/d2sc01103d
Sharma R, Kumar A. An expeditious and clean synthesis of novel benzotriazole-triazole conjugates via copper-catalyzed azide-alkyne cycloaddition click protocol (CuAAC). J Chem Sci. 2022;134:69. doi:10.1007/s12039-022-02073-x
Peters SJ, Patel K. Electron distribution in 1,2,3-benzotriazole and 1,2,3-triazole anion radical isomers: An EPR and DFT study. J Org Chem. 2021;86:14786-14796. doi:10.1021/acs.joc.1c01584
Hooper A, Macdonald JD, Reilly B, Maw J, Wirrick AP, Han SH, Lindsey AA, Rico EG, Romigh T, Goins CM, Wang NS, Stauffer SR. SARS-CoV-2 3CL-protease inhibitors derived from ML300: investigation of P1 and replacements of the 1,2,3-benzotriazole. Med Chem Res. 2023;32:1383-1390. doi:10.1007/s00044-023-03108-9
Yu J, Singh AS, Yan G, Yu J, Tiwari VK. Recent developments on denitrogenative functionalization of benzotriazoles. Synthesis. 2020;52:3781-3800. doi:10.1055/s-0040-1707253
Wu L, Zhao X, Bi E. Predicting the effect of dissolved humic acid on sorption of benzotriazole to biochar. Biochar. 2022;4:15. doi:10.1007/s42773-022-00134-5
Ibrahim DA, Khalaf SD, Ahmed NAA, Dalaf AH. Synthesis, characterization and biological evaluation (antifungal and antibacterial) of new derivatives of indole, benzotriazole and thioacetyl chloride. Mater Today Proc. 2021;47:6201-6210. doi:10.1016/j.matpr.2021.05.160
Jimoh TA, Oyewale AO, Ibrahim H, Habila JD, Arthur DE. Biological evaluation and docking study of synthesized derivatives of benzotriazole and benzimidazole as antibacterial agents. Chem Afr. 2022;5:509-523. doi:10.1007/s42250-022-00348-x
Jimoh TA, Oyewale AO, Ibrahim H, Habila JD, Arthur DE. Some benzotriazole and benzimidazole derivatives as antifungal agents for Candida Species: A molecular docking study. Chem Afr. 2022;6:383-391. doi:10.1007/s42250-022-00498-y
Singh N, Abrol V, Parihar S, Kumar S, Khanum G, Mir JM, Dar AA, Jaglan S, Sillanpää M, Al-Farraj S. Design, synthesis, molecular docking, and in vitro antibacterial evaluation of benzotriazole-based β‑amino alcohols and their corresponding 1,3-oxazolidines. ACS Omega. 2023;8:41960-41968. doi:10.1021/acsomega.3c07315
Singh A, Kaur K, Kaur H, Mohana P, Arora S, Bedi N, Chadha R, Bedi PMS. Design, synthesis and biological evaluation of isatin-benzotriazole hybrids as new class of anti-Candida agents. J Mol Struct. 2023;1274:134456. doi:10.1016/j.molstruc.2022.134456
Singh N, Mahant V, Bhasin R, Verma K, Kumar A, Vyas A. Antimicrobial and computational studies of newly synthesized benzotriazoles. Indian J Microbiol. 2024;64:1339-1346. doi:10.1007/s12088-024-01344-0
Aye M, Jarrahpour A, Haghighijoo Z, Heiran R, Pournejati R, Karbalaei-Heidari HR, Sinou V, Brunel JM, Akkurt M, Özdemir N, Turos E. Novel benzotriazole-β-lactam derivatives as antimalarial agents: Design, synthesis, biological evaluation and molecular docking studies. Chem Biodiversity. 2024;21:e202301745. doi:10.1002/cbdv.202301745
Kumari A, Kumar S. Synthesis, computational studies of new thymol derived chalcones and their benzotriazoles as antimicrobial agents. Lett Drug Des Discov. 2025;22:100029. doi:10.1016/j.lddd.2025.100029
Corona P, Piras S, Ibba R, Riu F, Murineddu G, Sanna G, Madeddu S, Delogu I, Loddo R, Carta A. Antiviral activity of benzotriazole based derivatives. Open Med Chem J. 2020;14:83-98. doi:10.2174/1874104502014010083
Ibba R, Piras S, Corona P, Riu F, Loddo R, Delogu I, Collu G, Sanna G, Caria P, Dettori T, Carta A. Synthesis, antitumor and antiviral in vitro activities of new benzotriazole-dicarboxamide derivatives. Front Chem. 2021;9:660424. doi:10.3389/fchem.2021.660424
Ibba R, Corona P, Nonne F, Caria P, Serreli G, Palmas V, Riu F, Sestito S, Nieddu M, loddo R, Sanna G, Piras S, Carta A. Design, synthesis, and antiviral activities of new benzotriazole-based derivatives. Pharmaceuticals. 2023;16:429. doi:10.3390/ph16030429
D’Souza S, Balaji S, Prema KV. QSAR, molecular docking, molecular dynamics and MM-GBSA approach for identification of prospective benzotriazole-based SARS-CoV 3CL protease inhibitors. J Biomol Struct Dyn. 2022;40:14247-14261. doi:10.1080/07391102.2021.2002718
Fetouh HA, Abd-Elnaby HM, Alsubaie MS, Sallam ER. New experimental low-cost nanoscience technology for formulation of silver nanoparticles-activated carbon composite as a promising antiviral, biocide, and efficient catalyst. J Exp Nanosci. 2022;17:297-314. doi:10.1080/17458080.2022.2068794
Himmi B, Brandán SA, Sert Y, Kawther AA, Dege N, Cinar EB, El Louzi A, Bougrin K, Karrouchi K. A quinoline-benzotriazole derivative: Synthesis, crystal structure and characterization by using spectroscopic, DFT and molecular docking methods. ResChem. 2023;5:100916. doi:10.1016/j.rechem.2023.100916
Li Z-X, Ding Y, Zhang T-H, Hu J-H, Luo R-S, Zhou X, Liu L-W, Yang S. Identification of novel bisamide-decorated benzotriazole derivatives as anti-phytopathogenic virus agents: Bioactivity evaluation and computational simulation. J Agric Food Chem. 2024;72:6900-6912. doi:10.1021/acs.jafc.3c06806
Marzec E, Poznanski J, Paprocki D. Thermodynamic contribution of iodine atom to the binding of heterogeneously polyhalogenated benzotriazoles by the catalytic subunit of human protein kinase CK2. IUBMB Life. 2020;72:1203-1210. doi:10.1002/iub.2257
Kumar MR, Dhayabaran VV, Sudhapriya N, Manikandan A, Gideon DA, Annapoorani S. p-TSA.H2O mediated one-pot, multi-component synthesis of isatin derived imidazoles as dual-purpose drugs against inflammation and cancer. Bioorg Chem. 2020;102:104046. doi:10.1016/j.bioorg.2020.104046
Khayyat AN, Mohamed KO, Malebari AM, El-Malah A. Design, synthesis, and antiproliferative activity of novel substituted imidazole-thione linked benzotriazole derivatives. Molecules. 2021;26:5983. doi:10.3390/molecules26195983
Paprocki D, Winiewska‑Szajewska M, Speina E, Kucharczyk R, Poznański J. 5,6‑diiodo‑1H‑benzotriazole: new TBBt analogue that minutely affects mitochondrial activity. Sci Rep. 2021;11:23701. doi:10.1038/s41598-021-03136-8
Riu F, Ibba R, Zoroddu S, Sestito S, Lai M, Piras S, Sanna L, Bordoni V, Bagella L, Carta A. Design, synthesis, and biological screening of a series of 4’-fluoro-benzotriazole-acrylonitrile derivatives as microtubule-destabilising agents (MDAs). J Enzyme Inhib Med Chem. 2022;37:2223-2240. doi:10.1080/14756366.2022.2111680
Qadri T, Aziz M, Channar PA, Ejaz SA, Hussain M, Attaullah HM, Ujan R, Hussain Z, Zehra T, Saeed A, Shah MR, Ogaly HA, Al-Zahrani FAM. Synthesis, biological evaluation and in silico investigations of benzotriazole derivatives as potential inhibitors of NIMA related kinase. RSC Adv. 2023;12:33826-22843. doi:10.1039/d3ra06149c
Aleksandrova YR, Nikolaeva NS, Shagina IA, Smirnova KD, Zubishina AA, Khlopotinin AI, Fakhrutdinov AN, Khokhlov AL, Begunov RS, Neganova ME. N-Aryl benzimidazole and benzotriazole derivatives and their hybrids as cytotoxic agents: Design, synthesis and structure–activity relationship studies. Molecules. 2024;29:5360. doi:10.3390/molecules29225360
Kumar A, Singh B, Sengupta S, Singh P, Ghate M, Yadav AK, Gang M, Kumar D. Design and synthesis of 2-substituted phenyl-4,5-diphenyl imidazole linked benzotriazoles: Anti-breast cancer activity, cell cycle analysis, apoptosis assay, and in silico studies. J Mol Struct. 2026;1349:143564. doi:10.1016/j.molstruc.2025.143564
Mioc M, Mioc A, Prodea A, Milan A, Balan-Porcarasu M, Racoviceanu R, Ghiulai R, Iovanescu G, Macasoi I, Draghici G, Dehelean C, Soica C. Novel triterpenic acid—benzotriazole esters act as pro-apoptotic antimelanoma agents. Int J Mol Sci. 2022;23:9992. doi:10.3390/ijms23179992
Anwar S, Singh V, Nirala RK, Prabha S, Athar F, Kumar S, Thakur SC. Synthesis of benzotriazole based azetidinone derivatives and their evaluation on calcium oxalate crystallization. Korean J Physiol Pharmacol. 2023;27:552-563.
Wang X, Du J, Zhou T, Fang X, Yang H. Novel benzotriazole-benzimidazole metal complexes: structure-activity relationship, synthesis, characterization, and antidiabetic activity. J Mol Struct. 2023;1292:136141. doi:10.1016/j.molstruc.2023.136141
Khan I, Rehman W, Rahim F, Hussain R, Khan S, Fazil S, Rasheed L, Taha M, Shah SAA, Abdellattif MH, Farghaly TA. Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking study of new benzotriazole-based bis-schiff base derivatives. Pharmaceuticals. 2023;16:17. doi:10.3390/ph16010017
Hayat S, Othman MS, Ullah H, Qureshi A, Rahim F, Begum S, Nawaz M, Wadood A, Al-Bagawi AH, Aref AM, Fareid MA, Iqbal R. Res Chem. 2025;15:102237. doi:10.1016/j.rechem.2025.102237
Pandya KM, Dave BP, Patel AH, Patel RJ, Patel JT, Desai PS. Synthesis, pharmacological evaluation and structure-activity relationship study of hydrazones. Asian J Green Chem. 2020;4:416-433.
Jayaseelan K, Senthilkumar SK, Arunagiri M, Bhavadharani S, Deepalakshmi G, Surya V. Design, docking, synthesis, characterization and biological evaluation of benzotriazole fused with oxadiazole derivative. World J Pharm Res. 2025;14:857-873.
Cheema ZM, Nisar M, Gondal HY, Alhussain SA, Zaki MEA, Coldham I. J Saudi Chem Soc. 2023;27:101746. doi:10.1016/j.jscs.2023.101746
Singh A, Sharma S, Arora S, Attri S, Kaur P, Gulati HK, Bhagat K, Kumar N, Singh H, Singh JV, Bedi PMS. New coumarin-benzotriazole based hybrid molecules as inhibitors of acetylcholinesterase and amyloid aggregation. Bioorg Med Chem Lett. 2020;30:127477. doi:10.1016/j.bmcl.2020.127477
Zapico JM, Acosta L, Pastor M, Rangasamy L, Marquez-Cantudo L, Coderch C, Ortin I, Nicolau-Sanus M, Puchades-Carrasco L, Pineda-Lucena A, Majali-Martinez A, Ramos P, dePascual-Teresa B, Ramos A. Design and synthesis of water-soluble and potent MMP-13 inhibitors with activity in human Osteosarcoma cells. Int J Mol Sci. 2021;22:9976. doi:10.3390/ijms22189976
Metri S, Shirke D, Babar V, Kolageri S. An overview on biological behavior of benzotriazole: Synthesis and docking study on its versatile biological activities. J Adv Zool. 2024;45:1230-1241. doi:10.53555/jaz.v45i2.4105
DOI: https://doi.org/10.15826/chimtech.9044
Copyright (c) 2025 Pakin Noppawan, Kanokkan Worawut, Suthida Kunnasut, Potchanee Keawkumsan, Baramee Phungpis

This work is licensed under a Creative Commons Attribution 4.0 International License.
Chimica Techno Acta, 2014–2025
eISSN 2411-1414
Copyright Notice






