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
CONDITIONS
反应条件
- 温度
- 40 °C
PROCEDURE
实验过程
To a mixture of 6-(4-hydroxy-phenyl)-3-methyl-1-(tetrahydro-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (215 mg), DIPEA (313 μL) and 1-benzyl-4-methyl-piperidin-4-ylamine (175 mg) in dichloroethane (7 mL), which was being stirred at 40° C., was added BEP (200 mg). The mixture was stirred at 40° C. for 60 min, then at r.t. overnight. Water was added and the mixture was extracted with dichloromethane. To the dichloromethane phase 30% sodium methoxide in methanol (0.4 mL) was added and stirred for 30 min. The mixture was filtered and the filtrate was washed with water, dried over magnesium sulfate and concentrated. The residue was chromatographed over silica (dichloromethane/methanol gradient) to give 1420 g (43%) of the title compound.
WORKUP
后处理
- additionwas added BEP (200 mg)
- stirringThe mixture was stirred at 40° C. for 60 min
- customat r.t.
- customovernight
- extractionthe mixture was extracted with dichloromethane
- additionTo the dichloromethane phase 30% sodium methoxide in methanol (0.4 mL) was added
- stirringstirred for 30 min
- filtrationThe mixture was filtered
- washthe filtrate was washed with water
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customThe residue was chromatographed over silica (dichloromethane/methanol gradient)