Events The 17th International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

This submission belongs to the session c. Microwave Assisted Synthesis of the event The 17th International Electronic Conference on Synthetic Organic Chemistry

Published date

31 Oct, 2013

Citation

Isabel Garcia-Santos, Rodríguez-González Iria, Castiñeiras Alfonso, Microwave assisted synthesis, the most efficient method for the synthesis of thiazolidin-4-ones from thiosemicarbazones, in Proceedings of The 17th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2013, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-17-c008

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Microwave assisted synthesis, the most efficient method for the synthesis of thiazolidin-4-ones from thiosemicarbazones

Isabel Garcia-Santos ¹

Rodríguez-González Iria ²

Castiñeiras Alfonso ¹

1. Department of Inorganic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain

2. Universidad de Santiago de Compostela

Abstract

(2-(pyrazin-2-yl)aminmethylenehydrazono)-thiazolidin-4-one, HPzAm4DHotaz, and (2-(pyrazin-2-yl)aminmethylenehydrazono)-3-methylthiazolidin-4-one, PzAm4Motaz have been prepared by the reaction of thiosemicarbazones with chloroacetic acid in presence of triethylamine in toluene using a microwave assisted synthesis and a conventional method, at reflux temperature. While the conventional method carried out other side products as triazoles and thiadiazoles, the cyclization of the thiosemicarbazones using microwave irradiation favours the obtaining of the tiazolidinones as only product and gave better yields, shorter times and any side products were formed

Keywords

thiosemicarbazone

thiazolidin-4-one

microwave synthesis

Manuscript

14ECSOCGarcia-Santos.pdf

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