Ultrasound-assisted synthesis of isatin-type 5′-(4-alkyl/aryl-1H-1,2,3-triazoles) via 1,3-dipolar cycloaddition reactions

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Abstract

This short report describes the preparation of twelve isatin derivatives, 5′-(4-alkyl/aryl-1H- 1,2,3-triazoles), using 5-azido-spiro[1,3-dioxolane-2,3′-indol]-2′(1′H)-one in the presence of various alkynes under acidic conditions and ultrasound irradiation. Compared with conventional methods, yields increased to 78-98%, and reaction times decreased to 5 min. Besides time and energy saving, there was no need for purification of the product by column chromatography on silica gel, generating less waste and spent solvent.

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Silva, B. N. M., Pinto, A. C., Silva, F. C., Ferreira, V. F., & Silva, B. V. (2016). Ultrasound-assisted synthesis of isatin-type 5′-(4-alkyl/aryl-1H-1,2,3-triazoles) via 1,3-dipolar cycloaddition reactions. Journal of the Brazilian Chemical Society, 27(12), 2378–2382. https://doi.org/10.5935/0103-5053.20160121

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