“…1-(3,4-Dihydroxybenzaldehyde)-2-acetylpyridiniumchloride hydrazone was prepared as previously reported [24] by heating under reflux 5 g of GP with 3.7 g 3,4-dihydroxybenzaldehyde in 10 ml absolute ethanol and few drops of glacial acetic acid on a water bath for 4 h till yellow precipitate, filtered off, recrystallized from ethanol and dried in a vacuum desiccator over anhydrous CaCl 2 , m.p., 281-282 • C. Scheme 1. DAPCH-Duolite C20.…”