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
- 25 °C
PROCEDURE
实验过程
To 634 g of sodium carbonate (5.98 mol) was added 2.91 kg of water under a nitrogen atmosphere, followed by stirring for dissolution. To the solution were added 3.0 L of tetrahydrofuran, 431 g of 3-aminophenyl boronic acid monohydrate (2.78 mol), 30.4 g of triphenylphosphine (0.116 mol) and 26.0 g of dichloropalladium (0.116 mol) in this order. To the mixture was dropwise added a solution of 2,4-dichloro-6,7-dimethoxyquinazoline (600 g; 2.32 mol) in tetrahydrofuran (12.0 L) over 2 hours while stirring at 60° C., followed by stirring at the same temperature for 16 hours. To the mixture were added 3.0 kg of a 5% sodium chloride solution and 12.0 L of tetrahydrofuran in this order, and the mixture was stirred at 50° C. for 1 hour and allowed to cool down to 25° C. The mixture was filtered through celite to remove the insoluble matter, and the filtrate was transferred to separatory funnel and the organic layer was separated. To the organic layer were added 150 g of anhydrous magnesium sulfate and 60.0 g of activated carbon, and the mixture was stirred at 50° C. for 1 hour and allowed to cool down to 25° C. The mixture was filtered through celite to remove the insoluble matter, and the filtrate was concentrated under reduced pressure. To the residue was added 6.0 L of water, and the mixture was stirred at room temperature for 1 hour. The precipitated crystals were filtered, and the crystals were dried at 50° C. under reduced pressure to yield 730 g of a target product. Yield: 62.1%
WORKUP
后处理
- stirringwhile stirring at 60° C.
- stirringby stirring at the same temperature for 16 hours
- stirringthe mixture was stirred at 50° C. for 1 hour
- filtrationThe mixture was filtered through celite
- customto remove the insoluble matter
- customthe filtrate was transferred to separatory funnel
- customthe organic layer was separated
- additionTo the organic layer were added 150 g of anhydrous magnesium sulfate and 60.0 g of activated carbon
- stirringthe mixture was stirred at 50° C. for 1 hour
- temperatureto cool down to 25° C
- filtrationThe mixture was filtered through celite
- customto remove the insoluble matter
- concentrationthe filtrate was concentrated under reduced pressure
- additionTo the residue was added 6.0 L of water
- stirringthe mixture was stirred at room temperature for 1 hour
- filtrationThe precipitated crystals were filtered
- customthe crystals were dried at 50° C. under reduced pressure