HRID924500

反应详情

EQUATION

反应方程式

HRID 924500 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of tert-butyl [(3R,4R,5S)-4-{[tert-butyl(dimethyl)silyl]oxy}-5-methyl-1-(3-nitropyridin-4-yl)piperidin-3-yl]carbamate (13.4 g, 28.7 mmol) in MeOH (80 mL) was hydrogenated in the presence of 10% palladium on carbon (4.6 g) under 60 psi of hydrogen for 16 h. The reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated under reduced pressure to give the sub-title compound (12.5 g, 99%). LCMS calc. for C22H41N4O3Si (M+H)+: m/z=437.3. Found: 437.4.

WORKUP

后处理

  1. filtrationThe reaction mixture was filtered through diatomaceous earth
  2. concentrationthe filtrate was concentrated under reduced pressure