Issue 4, 2000

Rapid synthesis of 2-cyanobenzothiazole, isothiocyanate and cyanoformanilide derivatives of dapsone

Abstract

New derivatives of the leprostatic drug dapsone are prepared by way of imino-1,2,3-dithiazoles obtained by condensation of aromatic primary bisamines, including dapsone, with 4,5-dichloro-1,2,3-dithiazolium chloride (Appel salt). Reactions, including microwave irradiation, initiated by nucleophilic attack at different sites of the dithiazole ring transform the bisiminodithiazoles into the symmetrical, and some unsymmetrical, title compounds.

Article information

Article type
Paper
Submitted
02 Nov 1999
Accepted
08 Dec 1999
First published
03 Feb 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 563-566

Rapid synthesis of 2-cyanobenzothiazole, isothiocyanate and cyanoformanilide derivatives of dapsone

T. Besson, J. Guillard and C. W. Rees, J. Chem. Soc., Perkin Trans. 1, 2000, 563 DOI: 10.1039/A908742G

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