A wide range of methods exist for forming substituted 1,2,3-triazoles.[4] These include the Banert cascade or the azide alkyne Huisgen cycloaddition in which an azide and an alkyne undergo a 1,3-dipolar cycloaddition reaction. Under thermal conditions, regioselectivity is substrate dependent. Selectivity can be increased with metal catalysts, which have the added benefit of reacting without excessive or extensive heating. Copper catalyzed cycloadditions favor 1,4-disubstituted triazoles, Ruthenium catalyzed cycloaddition favor 1,5-disubstituted triazoles. This chemistry was expanded by Zhu et al. in 2018 wherein they report a two-step sequence from a terminal alkyne to 4-cyano 1,5-disubstituted triazoles. [5]
The 2H-1,2,3-triazole tautomer is the major form in aqueous solution.[6]
It is a surprisingly stable structure compared to other organic compounds with three adjacent nitrogen atoms. However, flash vacuum pyrolysis at 500 °C leads to loss of molecular nitrogen (N2) leaving a three-member aziridine ring. Certain triazoles are relatively easy to cleave due to ring–chain tautomerism. One manifestation is found in the Dimroth rearrangement.
1,2,3-Triazole finds use in research as a bioisostere in medicinal chemistry[7] building block for more complex chemical compounds, including pharmaceutical drugs such as mubritinib and tazobactam.
^Gilchrist, T.L. (1987). Heterocyclic chemistry. Prentice Hall Press. ISBN0-582-01421-2.
^Song, Lei; Ang, Hwee Ting; Senthilperumal, Jagadeesan; Kanusu, Umamaheswara Rao; Venugopal, Sivasankaran; Rangarajan, Naveen; Krishnamoorthy, Shivasankar; Dubbaka, Srinivas Reddy; O’Neill, Patrick; Wu, Jie (12 March 2024). "1,2,3-Triazole Synthesis: Development of Safe and Effective Batch and Continuous Manufacturing Processes". Organic Process Research & Development. doi:10.1021/acs.oprd.4c00020.
^Krivopalov, Victor P; Shkurko, Oleg P (30 April 2005). "1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring". Russian Chemical Reviews. 74 (4): 339–379. doi:10.1070/RC2005v074n04ABEH000893.
^Liu, P.; Clark, R.; Zhu, L. (2018). "Synthesis of 1‑Cyanoalkynes and Their Ruthenium(II)-Catalyzed Cycloaddition with Organic Azides to Afford 4‑Cyano-1,2,3-triazoles". J. Org. Chem.83 (9): 5092–5103. doi:10.1021/acs.joc.8b00424. PMID29630830.
