反应详情

温度

0 °C

A stirred mixture of (S)-2-(2-Oxo-2H-pyridin-1-yl)-propionic acid (70 mg, 0.42 mmol), 3-Amino-5-fluoro-4-hydroxy-pentanoic acid tert-butyl ester (91 mg, 0.44 mmol), HOAt (63 mg, 0.46 mmol) and DMAP (59 mg, 0.48 mmol) and anhydrous THF (5 ml) was cooled to 0° C. then EDC (88 mg, 0.46 mmol) was added. The mixture was allowed to warm to room temperature during 16 h then concentrated under reduced pressure. The residue was purified by flash chromatography (3% methanol in ethyl acetate) to afford the title compound as a white foam (137 mg, 92%): 1H NMR (400 MHz, CDCl3) δ 1.3-1.5 9H, 2×s), 2.5-2.7 2H, m), 3.4-3.7 1H, m), 3.9-4.6 4H, m), 5.4-5.6 1H, m), 6.2-6.3 1H, m), 6.5-6.6 1H, m), 7.1-7.6 3H, m); 19F NMR (376 MHz, CDCl3) δ −230.14, −230.14, −230.17, −230.95, −231.07.

1. temperatureto warm to room temperature during 16 h
2. concentrationthen concentrated under reduced pressure
3. customThe residue was purified by flash chromatography (3% methanol in ethyl acetate)