HRID41491

反应详情

EQUATION

反应方程式

HRID 41491 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

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

  1. stirringwhile stirring at 60° C.
  2. stirringby stirring at the same temperature for 16 hours
  3. stirringthe mixture was stirred at 50° C. for 1 hour
  4. filtrationThe mixture was filtered through celite
  5. customto remove the insoluble matter
  6. customthe filtrate was transferred to separatory funnel
  7. customthe organic layer was separated
  8. additionTo the organic layer were added 150 g of anhydrous magnesium sulfate and 60.0 g of activated carbon
  9. stirringthe mixture was stirred at 50° C. for 1 hour
  10. temperatureto cool down to 25° C
  11. filtrationThe mixture was filtered through celite
  12. customto remove the insoluble matter
  13. concentrationthe filtrate was concentrated under reduced pressure
  14. additionTo the residue was added 6.0 L of water
  15. stirringthe mixture was stirred at room temperature for 1 hour
  16. filtrationThe precipitated crystals were filtered
  17. customthe crystals were dried at 50° C. under reduced pressure