HRID41492

反应详情

EQUATION

反应方程式

HRID 41492 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

Two hundred grams of crude 3-(2-chloro-6,7-dimethoxyquinazolin-4-yl)phenylamine (content 124 g; 0.394 mol) was suspended in a mixed solution of 1.2 L of tetrahydrofuran and 0.6 L of isopropanol. To the mixture was added 1.2 L of a methylamine solution in methanol, and the mixture was stirred in a SUS autoclave at 90° C. for 15 hours. The reaction mixture was allowed to cool down to 25° C., and concentrated under reduced pressure. To the residue were added 1.0 L of water and 4.0 L of chloroform, and the mixture was stirred at 50° C. for 0.5 hours 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 50.0 g of anhydrous magnesium sulfate and 20.0 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 904 mL of chloroform, and the mixture was stirred at 50° C. for 1 hour and stirred overnight after turning off the heater. Then the mixture was stirred in an ice bath for 2 hours and precipitated crystals were filtered, and the crystals were dried at 50° C. under reduced pressure to yield 76.3 g of a target product. Yield: 38.7%

WORKUP

后处理

  1. temperatureto cool down to 25° C.
  2. concentrationconcentrated under reduced pressure
  3. additionTo the residue were added 1.0 L of water and 4.0 L of chloroform
  4. stirringthe mixture was stirred at 50° C. for 0.5 hours
  5. temperatureto cool down to 25° C
  6. filtrationThe mixture was filtered through celite
  7. customto remove the insoluble matter
  8. customthe filtrate was transferred to separatory funnel
  9. customthe organic layer was separated
  10. additionTo the organic layer were added 50.0 g of anhydrous magnesium sulfate and 20.0 g of activated carbon
  11. stirringthe mixture was stirred at 50° C. for 1 hour
  12. temperatureto cool down to 25° C
  13. filtrationThe mixture was filtered through celite
  14. customto remove the insoluble matter
  15. concentrationthe filtrate was concentrated under reduced pressure
  16. additionTo the residue was added 904 mL of chloroform
  17. stirringthe mixture was stirred at 50° C. for 1 hour
  18. stirringstirred overnight
  19. stirringThen the mixture was stirred in an ice bath for 2 hours
  20. customprecipitated crystals
  21. filtrationwere filtered
  22. customthe crystals were dried at 50° C. under reduced pressure