Abstract
Environmentally and economically benign solvent free syntheses of thioethers are performed by the reaction of benzothiazole thiol with different halides on basic alumina—a simple, cheap, robust catalyst that couples a range of substrates with thiol in excellent yields in a short time. The in vitro antibacterial screening of compounds 3c, e, g, i, j, and k were evaluated against the Gram-positive organism Staphylococcus aureus and Gram-negative organisms. Escherichia coli and Proteus mirabilis by the Agar well diffusion method.
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Acknowledgments
We thank Syngene International Ltd., Bangalore, India, for its generous support in spectral analysis. F. N. Khan thanks the DST, India, for Fast Track Young Scientist fellowship.
Notes
a Benzothiazole thiol 1 (1 equiv) and 1-(chloromethyl)-4-chlorobenzene- 2a (1.2 equiv).