반응 #83776

ord-534a5452e3d1451ca980900efc33a77e

용매

반응 조건

온도
85°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도under reflux for 2.5 hours
  3. 3
    온도was then heated
  4. 4
    온도under reflux for 2.5 hours
  5. 5
    기타At the end of this time, the reaction mixture was freed from the solvent by evaporation under reduced pressure
  6. 6
    workup.ADDITION80 ml of toluene and 19.1 g of sodium carbonate were added to the residue
  7. 7
    기타thus obtained
  8. 8
    기타At the end of this time, the insoluble material in the reaction mixture was removed by filtration
  9. 9
    세척The filtrate was washed with water
  10. 10
    건조dried over anhydrous sodium sulfate
  11. 11
    기타after which the solvent was removed by distillation under reduced pressure
  12. 12
    기타The resulting residue was crystallized by trituration with 2-propanol

실험 절차

A mixture of 10.3 g of 2-hydroxy-3-nitropyridine and 25.5 ml of thionyl chloride was heated under reflux for 2.5 hours, after which 1.1 ml of dimethylformamide were rapidly added to the mixture, which was then heated under reflux for 2.5 hours. At the end of this time, the reaction mixture was freed from the solvent by evaporation under reduced pressure. 80 ml of toluene and 19.1 g of sodium carbonate were added to the residue thus obtained, and then a solution of 12.3 ml of 4-chlorobenzylamine in 20 ml of toluene was added dropwise to the resulting mixture, which was then stirred at 85° C. for 4 hours. At the end of this time, the insoluble material in the reaction mixture was removed by filtration. The filtrate was washed with water and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The resulting residue was crystallized by trituration with 2-propanol, to give 12.0 g of the title compound, melting at 95°-96° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05624935uspto-grants-1997_04