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 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 1,4-dioxane (40 mL), 296e (588 mg, 3.0 mmol), 3,5-dibromo-1-methylpyridin-2(1H)-one (800 mg, 3.0 mmol), and cesium carbonate (1.96 g, 6.0 mmol). After bubbling nitrogen through the suspension for 20 minutes, xantphos (173 mg, 0.30 mmol) and tris(dibenzylideneacetone)dipalladium(0) (137 mg, 0.15 mmol) were added. The system was subjected to three cycles of vacuum/argon flush and heated at reflux for 5 h. It was then cooled to room temperature and filtered. The solid was washed with dichloromethane (2×15 mL). The combined filtrate was concentrated under reduced pressure. The residue solid was purified by silica-gel column chromatography eluting with dichloromethane/methanol (80/1 to 30/1) to afford 296f (745 mg, 65%) as yellow solid. MS-ESI: [M+H]+ 382.9
WORKUP
后处理
- customA 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser
- customAfter bubbling nitrogen through the suspension for 20 minutes
- customflush
- temperatureheated
- temperatureat reflux for 5 h
- filtrationfiltered
- washThe solid was washed with dichloromethane (2×15 mL)
- concentrationThe combined filtrate was concentrated under reduced pressure
- customThe residue solid was purified by silica-gel column chromatography
- washeluting with dichloromethane/methanol (80/1 to 30/1)