反应 #1244321

反应方程式

5-fluoro-4-hydroxy-3-[1-(benzyloxycarbonyl)-2-piperidinecarboxamido]-pentanoic acid tert-butyl ester

→

5-Fluoro-4-hydroxy-3-[2-piperidinecarboxamido]-pentanoic acid tert-butyl ester

溶剂

ethyl acetate

反应条件

后处理

1. 1
   其他The reaction mixture was then thoroughly degassed
2. 2
   过滤was filtered through celite
3. 3
   浓缩concentrated to the sub-title compound as a colorless gum (5.17 g, 100%)

实验过程

A stirred solution of [3S/R,4S/R,(2S)]-5-fluoro-4-hydroxy-3-[1-(benzyloxycarbonyl)-2-piperidinecarboxamido]-pentanoic acid tert-butyl ester (7.37 g, 16.29 mmol) in ethyl acetate (150 ml) was treated with 10% Pd/C (830 mg). The reaction mixture was then thoroughly degassed and placed under a hydrogen balloon. The resulting mixture was stirred at room temperature for 3 hrs after which it was filtered through celite and concentrated to the sub-title compound as a colorless gum (5.17 g, 100%): 1H NMR (400 MHz, CDCl3) δ 1.16-2.00 (15H, m), 2.51-2.78 (3H, m), 2.99-3.09 (1H, m), 3.18-3.28 (1H, m), 3.93-4.56 (4H, m), 7.39-7.58 (1H, m); 19F (376 MHz, CDCl3) δ −229.34 (t), −229.42 (t), −229.87 (t), 230.02 (t).

来源