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Wiley, Journal of Heterocyclic Chemistry, 6(51), p. 1856-1861, 2014

DOI: 10.1002/jhet.1856

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Microwave and Ultrasound-Assisted Synthesis of Thiosemicarbazones and Their Corresponding (4,5-Substituted-thiazol-2-yl)hydrazines: Microwave and Ultrasound-Assisted Synthesis of (Thiazolyl)hydrazines

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Hantzsch cyclization of thiosemicarbazone intermediates is a very popular approach to the synthesis of substituted thiazoles. We developed a convenient microwave and ultrasound‐assisted method both for the synthesis of 1‐(alkyliden/cycloalkyliden/aryliden)thiosemicarbazone intermediates and their cyclization into (4,5‐substituted‐thiazol‐2‐yl)hydrazines. The search for optimal reaction conditions included the use of different catalysts (Lewis acids and resins) and solvents at discrete temperatures, pressures, and irradiation powers. Comparing yields, reaction times, and efforts proved that microwave and ultrasound‐assisted techniques outmatch conventional heating and have a remarkable influence on the synthesis.