Abstract:Abstract:The 7-acetyl-2-aryl-5-bromo-3-(trifluoroacetyl)indoles 1a-d were reacted with hydroxylamine hydrochloride (2.2 equiv.) in the presence of pyridine in ethanol under reflux to afford the corresponding diketo oxime derivatives 2a-d.Beckmann rearrangement of the latter with trifluoroacetic acid under reflux afforded the corresponding 7-acetamido-2-aryl-5-bromo-3-(trifluoroacetyloxime)indoles 3a-d. The structures of the prepared compounds were characterized using a combination of NMR ( 1 H & 13 C), IR, a… Show more
C8H6ClIO2, orthorhombic, Pbcn (no. 60), a = 13.3204(7) Å, b = 7.2517(4) Å, c = 18.5627(9) Å, V = 1793.07(16) Å3, Z = 8, Rgt(F) = 0.0195, wRref(F2) = 0.0483, T = 173 K.
C8H6ClIO2, orthorhombic, Pbcn (no. 60), a = 13.3204(7) Å, b = 7.2517(4) Å, c = 18.5627(9) Å, V = 1793.07(16) Å3, Z = 8, Rgt(F) = 0.0195, wRref(F2) = 0.0483, T = 173 K.
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