Reaktion #83776

ord-534a5452e3d1451ca980900efc33a77e

Reaktionsgleichung

NCc1ccc(Cl)cc1
4-chlorobenzylamine
O=[N+]([O-])c1cccnc1O
2-hydroxy-3-nitropyridine
O=S(Cl)Cl
thionyl chloride
CN(C)C=O
dimethylformamide
O=[N+]([O-])c1cccnc1NCc1ccc(Cl)cc1
title compound
O=[N+]([O-])c1cccnc1NCc1ccc(Cl)cc1
2-(4Chlorobenzyl)amino-3-nitropyridine

Lösungsmittel

Reaktionsbedingungen

Temperatur
85°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturunder reflux for 2.5 hours
  3. 3
    Temperaturwas then heated
  4. 4
    Temperaturunder reflux for 2.5 hours
  5. 5
    SonstigeAt 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
    Sonstigethus obtained
  8. 8
    SonstigeAt the end of this time, the insoluble material in the reaction mixture was removed by filtration
  9. 9
    WaschenThe filtrate was washed with water
  10. 10
    Trocknendried over anhydrous sodium sulfate
  11. 11
    Sonstigeafter which the solvent was removed by distillation under reduced pressure
  12. 12
    SonstigeThe resulting residue was crystallized by trituration with 2-propanol

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05624935uspto-grants-1997_04