Reaktion #452485

ord-0debfc1f785f4189a107bae53f0f3f30

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter the resulting mixture was heated
  2. 2
    Temperaturunder reflux
  3. 3
    workup.DISTILLATIONthe solvent was distilled off
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in acetone (50 ml)
  5. 5
    workup.STIRRINGThe thus-obtained mixture was stirred for 1 hour
  6. 6
    SonstigeA deposited precipitate was removed
  7. 7
    workup.DISTILLATIONthe solvent was distilled off
  8. 8
    workup.DISSOLUTIONThe residue was dissolved in ethyl ether
  9. 9
    WaschenThe resulting solution was washed with an aqueous solution of sodium chloride
  10. 10
    Trocknendried over anhydrous magnesium sulfate
  11. 11
    workup.DISTILLATIONThe solvent was distilled off
  12. 12
    workup.DISSOLUTIONthe residue was dissolved in methanol
  13. 13
    workup.ADDITIONfollowed by the addition of concentrated hydrochloric acid (5 ml) for acidification
  14. 14
    workup.DISTILLATIONThe solvent was distilled off
  15. 15
    Sonstigethe thus-obtained residue was crystallized from a mixed solvent of ethanol and methanol

Vorschrift

Thionyl chloride (6 ml) was added to a suspension of quinaldinic acid (3.463 g, 20 mmol) in chloroform (40 ml). After the resulting mixture was heated under reflux and stirring for 6 hours, the solvent was distilled off. The residue was dissolved in acetone (50 ml), followed by the addition of a solution of N-benzylpiperazine (10.576 g, 60 mmol) in acetone (50 ml). The thus-obtained mixture was stirred for 1 hour. A deposited precipitate was removed, and the solvent was distilled off. The residue was dissolved in ethyl ether. The resulting solution was washed with an aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was dissolved in methanol, followed by the addition of concentrated hydrochloric acid (5 ml) for acidification. The solvent was distilled off and the thus-obtained residue was crystallized from a mixed solvent of ethanol and methanol, whereby 7.166 g of the title compound were obtained as white powder (yield: 97.5%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06127360uspto-grants-2000_10