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
- 0 °C
PROCEDURE
实验过程
Sodium hydride (3.88 g of 60% dispersion in mineral oil, 0.097 mol) was added to 150 mL of dry DMF under nitrogen, and the reaction mixture was cooled in an ice bath. 2,4-Difluorophenol (8.85 mL, 0.092 mol) was added dropwise over 10 minutes (maintaining temperature between 5 and 10° C.), after which the reaction mixture was stirred for 15 minutes at 0° C., followed by 15 minutes of stirring at room temperature. A solution of 3-Iodo-6-methanesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidine (11.91 g, 0.026 mol) in 100 mL dry DMF was added, and the reaction mixture was heated to 140° C. for four hours while stirring under nitrogen. The reaction mixture was cooled to room temperature, and volatiles were removed under reduced pressure. The was added to 200 mL of 10% aqueous ammonium chloride, 50 mL water, and 250 mL EtOAc. The aqueous phase was partitioned off and extracted once with 250 mL EtOAc. The combined organic phases were washed with saturated aqueous brine, dried over MgSO4, filtered, and evaporated under reduced pressure to yield an oil. The oil was eluted through silica gel with hexanes EtOAc (20:1 to 10:1) to afford 6.23 g of 6-(2,4-Difluoro-phenoxy)-3-iodo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidine.
WORKUP
后处理
- temperaturethe reaction mixture was cooled in an ice bath
- temperature(maintaining temperature between 5 and 10° C.)
- waitfollowed by 15 minutes
- stirringof stirring at room temperature
- temperaturethe reaction mixture was heated to 140° C. for four hours
- stirringwhile stirring under nitrogen
- temperatureThe reaction mixture was cooled to room temperature
- customvolatiles were removed under reduced pressure
- additionThe was added to 200 mL of 10% aqueous ammonium chloride, 50 mL water, and 250 mL EtOAc
- customThe aqueous phase was partitioned off
- extractionextracted once with 250 mL EtOAc
- washThe combined organic phases were washed with saturated aqueous brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated under reduced pressure
- customto yield an oil
- washThe oil was eluted through silica gel with hexanes EtOAc (20:1 to 10:1)