Synthesis of 2-Alkyl-5-Mercaptotriazoles and their Derivatives as Antibacterial and Antifungal Agents

S. M. Kudari* and A. S. Sajjanshetty,

Department of Chemistry, Gulbarga University, Gulbarga - 584 106, Karnataka India.

ABSTRACT:

Ethyl stearate reacted with hydrazinehydrate (80%) to yield acid hydrazide. This on reaction with different isothiocyantes gave thiosemicarbazides, which were cyclised with sodium hydroxide (4%) togive 1-aryl/allyl-2-alkyl-5-mercaplo-1, 3, 4 triazoles (I,). These triazoles were reacted with ethyl chloroformate and hydrazinehydrate to yield corresponding hydrazides (IIIa-f). Hydrazines were condensed with aryl aldenydes to various acylhydrazones (IVa-1), which on treatment with thioglycollic acid afforded 4-thiazolidinones (Va-1). These compounds were characterised by ir, pmr spectral data and screened for antibacterial, antifungal activity.

KEYWORDS:

Ethyl; Synthesis; Derivatives; Antifungal

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Copy the following to cite this article: Rao V. S. Synthesis Of 2-Alkyl-5-Mercaptotriazoles And Their Derivatives As Antibacterial And Antifungal Agents. Orient J Chem 1995;11(1).

Copy the following to cite this URL: Rao V. S. Synthesis Of 2-Alkyl-5-Mercaptotriazoles And Their Derivatives As Antibacterial And Antifungal Agents. Orient J Chem 1995;11(1). Available from:http://www.orientjchem.org/?p=37990