反应详情

A solution of (2S)-2-[(1H-imidazole-2-carbonyl)-amino]-propionic acid and 3-amino-5-fluoro-4-hydroxy-pentanoic acid tert-butyl ester (0.254 g) in THF (7 mL) was cooled to 0° C. before addition of DMAP (0.151 g), diisopropylethyl amine (0.56 mL), HOBT (0.16 g) and EDC.HCl (0.23 g). The reaction mixture stirred at ambient temperature for 18 hrs before being concentrated at reduced pressure. The residue was purified by silica gel chromatography (5% methanol in dichloromethane) to afford the sub-title compound as a colourless solid (0.386 g, 97%): 1H NMR 400 MHz CDCl3/CD3OD 1.40 (12H, m), 3.92 (1H, m), 4.20–4.55 (4H, m), 7.11 (2H, d, J 15) 19F NMR CDCl3−229.74 (m), −229.84 (m), −230.54 (m), −230.87 (m).

1. concentrationbefore being concentrated at reduced pressure
2. customThe residue was purified by silica gel chromatography (5% methanol in dichloromethane)