Bromoacetyl bromide → HCID 131727451、化合物

反応式

[C:1]([O:5][C:6](=[O:14])[NH:7][C@@H:8]([CH3:13])[CH2:9][NH:10][CH2:11][CH3:12])([CH3:4])([CH3:3])[CH3:2].C(=O)(O)[O-].[Na+].[Br:20][CH2:21][C:22](Br)=[O:23]>C(OCC)(=O)C>[Br:20][CH2:21][C:22]([CH2:12][CH2:11][NH:10][CH2:9][C@@H:8]([NH:7][C:6](=[O:14])[O:5][C:1]([CH3:4])([CH3:3])[CH3:2])[CH3:13])=[O:23]

参加物

実験手順

To a cold (0° C.) stirred solution of tert-butyl[(1S)-2-(ethylamino)-1-methylethyl]carbamate (11.0 g, 54.6 mmol) in a mixture of ethyl acetate (107 mL) and saturated aqueous sodium bicarbonate (65 mL), bromoacetyl bromide (12.1 g, 60.0 mmol) was added portionwise under an atmosphere of nitrogen. The mixture was allowed to warm up to room temperature over a period of 3.5 hours. The organic phase was separated, washed successively with saturated aqueous sodium bicarbonate, and brine. The organic extract was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was concentrated as a solution in toluene under vacuum to afford the title compound. ES MS M+1=323, 325.