HRID30411

反应详情

EQUATION

反应方程式

HRID 30411 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-12 °C

PROCEDURE

实验过程

2-Amino-6-fluorobenzoic acid (2.00 g, 12.89 mmol) was combined with 2-fluorophenylhydrazine hydrochloride (2.096 g, 12.89 mmol) and HOBt (3.949 g, 25.79 mmol) in dry THF (75 ml) and cooled to about −12° C. N-Methylmorpholine (2.835 ml, 25.79 mmol) was added, the mixture was stirred for 5 minutes, then EDC hydrochloride (2.66 g, 13.88 mmol) was added. The mixture was maintained at a temperature between −14 and −10° C. for 1 hour, then allowed to slowly warm to room temperature and stirred for 18 hours. The mixture was cooled to 0° C., then filtered through CELITE® (diatomaceous earth). The filtrate was diluted with EtOAc, treated with saturated NaHCO3 and the layers separated. The organic layer was washed twice with 50% saturated NaHCO3 and then dried over MgSO4 and concentrated. The resulting solid was triturated with dichloromethane, filtered, rinsed with a very small amount of dichloromethane and dried. The filtrate from the trituration was re-triturated with a small amount of dichloromethane, filtered, rinsed with a tiny amount of dichloromethane and dried. The filtrate was concentrated to dryness, triturated with a small amount of Et2O, filtered, rinsed with a tiny amount of ether and dried. The three solids were combined to afford a total of 2.182 g (64%) of 2-amino-6-fluoro-benzoic acid N′-(2-fluoro-phenyl)-hydrazide (Intermediate 44) as an off-white solid. MS (APCI): (M−1)=262.0.

WORKUP

后处理

  1. temperatureThe mixture was maintained at a temperature between −14 and −10° C. for 1 hour
  2. temperatureto slowly warm to room temperature
  3. stirringstirred for 18 hours
  4. temperatureThe mixture was cooled to 0° C.
  5. filtrationfiltered through CELITE® (diatomaceous earth)
  6. additionThe filtrate was diluted with EtOAc
  7. additiontreated with saturated NaHCO3
  8. customthe layers separated
  9. washThe organic layer was washed twice with 50% saturated NaHCO3
  10. dry with materialdried over MgSO4
  11. concentrationconcentrated
  12. customThe resulting solid was triturated with dichloromethane
  13. filtrationfiltered
  14. washrinsed with a very small amount of dichloromethane
  15. customdried
  16. customThe filtrate from the trituration was re-triturated with a small amount of dichloromethane
  17. filtrationfiltered
  18. washrinsed with a tiny amount of dichloromethane
  19. customdried
  20. concentrationThe filtrate was concentrated to dryness
  21. customtriturated with a small amount of Et2O
  22. filtrationfiltered
  23. washrinsed with a tiny amount of ether
  24. customdried