3,4-Diaminophenol → HCID 178471172、化合物
反応式
[NH2:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[CH:6][C:7]=1[NH2:8].C(ON[C:14]([CH:16]([CH3:22])[C:17]([O:19][CH2:20][CH3:21])=[O:18])=N)C>C(O)C>[OH:9][C:4]1[CH:5]=[CH:6][C:7]2[NH:8][C:14]([CH:16]([CH3:22])[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[N:1][C:2]=2[CH:3]=1参加物
4
実験手順
A mixture comprising of 3,4-diaminophenol (3.661 g, 29.5 mL), ethyl 2-(N-ethoxyamidino)propionate (7.423 g, 38.4 mmol) and ethanol (30 mL) was heated at reflux for 6 hours and concentrated in vacuo. The residue was dissolved in ethyl acetate (200 mL) and the solution was washed with saturated aqueous sodium hydrogencarbonate (3×20 mL) and brine (1×20 mL), dried (MgSO4) and concentrated in vacuo to provide ethyl 2-(5-hydroxy-1H-benzoimidazol-2-yl)propionate (6.3 g, 91% yield) as a dark solid. The solid was further purified by silica gel flash chromatography (100% ethyl acetate); MS (PB-PCI) C12H14N2O3 m/e calc 234.28; found 235 (MH+).