135. 'Three-Component Reaction' with Aromatic Thioketones, Phenyl Azide, and Dimethyl Fumarate

Article abstract of DOI:10.1002/hlca.19970800617

The reaction of thiobenzophenone (= diphenylmethanethione; 8a) or 9H-fluorene-9-thione (8b) and methyl fumarate (9) in excess PhN₃ at 80° yields a mixture of diastereoisomeric thiiranes 10 and 11 (Scheme 1). A mechanism involving the initial formation of 1-phenyl-4,5-dihydro-1H-1,2,3-triazole-4,5-dicarboxylate 12 by 1,3-dipolar cycloaddition of PhN₃ and 9 is proposed in Scheme 2. The diazo compound 13, which is in equilibrium with 12, undergoes a further 1,3-dipolar cycloaddition with thioketones 8 to give 2,5-dihydro-1,3,4-thiadiazoles 14. Elimination of N₂ ylide the thiocarbonyl ylide 15 which cyclizes to the corresponding thiirane. Desulfurization of the thiiranes 10 and 11 with hexamethylphosphorous triamide leads to the olefinic compounds 16 (Scheme 3). The crystal structures of 1Oa, 11, and 16b were determined.