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The treatment of o-iodopropiolanilides (12), which were easily prepared from o-iodophenylisocyanate (11) and ethynylmagnesium bromide, with sodium hydrogen telluride resulted in the intramolecular ring closure of the presumed phenyltellurol intermediates (13) to a triple bond to give the 1,5-benzotellurazepin-4-ones (14) as the sole characterized products. The obtained amides (14) were easily converted into fully unsaturated lactim 4-methoxy-1,5-benzotellurazepines (18) by treatment with trimethyloxonium tetrafluoroborate. Decomposition by thermolysis of the 4-methoxyazepinenes (18) afforded the 4-methoxyquinolines (19) with extrusion of a tellurium atom.

chemical and pharmaceutical bulletin/chemical and pharmaceutical bulletin

Studies on Tellurium-Containing Heterocycles. Part 22. Tellurazepine Ring System: Preparation of 1,5-Benzotellurazepin-4-ones and Their Conversion into Fully Unsaturated 1,5-Benzotellurazepines