In connection with our studies on potential bioactive compounds some n
ew polysubstituted 3-thiocarbamoyrthiazolidines 5, 6, 7, 9 and 10 were
prepared in the reaction between 2-(2-methoxyphenyl)iminothiazolidine
(2) and sulfamoylphenyl isothiocyanates 3 and 4a-c. The structures fo
r compounds 2 and 5 were established by X-ray analyses, showing that t
he reaction is taking place at the endocyclic nitrogen atom of thiazol
idine ring.