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
A solution of methyl 3-[5-(dimethylcarbamoyl)pyrazin-2-yl]oxy-5-[(2S)-1-[(2-methylpropan-2-yl)oxy]propan-2-yl]oxy-benzoate (170 g, 0.39 mol) in formic acid (850 mL) was heated to 90° C. for 3 hours. Ethyl acetate (1700 mL), water (1700 mL) and saturated aqueous brine (850 mL) was added and the aqueous layer separated and extracted with ethyl acetate (850 mL) and the combined organic layers were washed with saturated aqueous brine (850 mL), dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved with ethyl acetate (1500 mL), water (1500 mL) and methanol (150 mL). Sodium carbonate (170 g) was added and the biphasic solution heated to reflux for 2 hours. The aqueous layer was separated and the organic layer washed with water (1700 mL). The combined aqueous phases were extracted with ethyl acetate (850 mL) and the combined organic layers dried (MgSO4) and evaporated under reduced pressure. The residue was purified by flash chromatography eluting with 100% ethyl acetate to obtain a the title compound (148 g).
WORKUP
后处理
- customthe aqueous layer separated
- extractionextracted with ethyl acetate (850 mL)
- washthe combined organic layers were washed with saturated aqueous brine (850 mL)
- dry with materialdried (MgSO4)
- customevaporated under reduced pressure
- dissolutionThe residue was dissolved with ethyl acetate (1500 mL), water (1500 mL) and methanol (150 mL)
- additionSodium carbonate (170 g) was added
- temperaturethe biphasic solution heated
- temperatureto reflux for 2 hours
- customThe aqueous layer was separated
- washthe organic layer washed with water (1700 mL)
- extractionThe combined aqueous phases were extracted with ethyl acetate (850 mL)
- dry with materialthe combined organic layers dried (MgSO4)
- customevaporated under reduced pressure
- customThe residue was purified by flash chromatography
- washeluting with 100% ethyl acetate