反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a stirred solution of 9-benzyloxy-2-isopropyl-6-(1-pyridin-2-yl-cyclopentylmethyl)-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione (440) (50 mg, 0.106 mmol) in ethanol (5 mL), Pd—C (10% w/w, 10 mg) was added and the reaction mixture was allowed to stir for 1 h in a hydrogen atmosphere at balloon pressure while silica thin layer chromatography was performed (10% methanol in dichloromethane; Rf=0.3). After completion of the reaction, the reaction mixture was filtered through a celite bed and concentrated to obtain a crude product which was purified by normal silica gel (100-200 mesh) column chromatography using 2-5% methanol in dichloromethane as a gradient polarity mobile phase to get 9-hydroxy-2-isopropyl-6-(1-pyridin-2-yl-cyclopentylmethyl)-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione (441) (26 mg, 64%) as an off-white solid.
WORKUP
后处理
- customAfter completion of the reaction
- filtrationthe reaction mixture was filtered through a celite bed
- concentrationconcentrated
- customto obtain a crude product which
- customwas purified by normal silica gel (100-200 mesh) column chromatography