Abstract
Bz-Amino-derivatives of benzothiazole readily underwent Ullmann–Fetvadjian condensation with naphthols and paraformaldehyde, to give thiazole isosteres of carcinogenic dibenzacridines; with 4-hydroxycoumarin, coumarinothiazoloquinolines were obtained. Bz-Hydrazinobenzothiazoles were successfully used for the preparation of thiazole isosteres of carcinogenic dibenzocarbazoles.
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