Reaktion #68054

ord-5e4ca8f422ae43e28b155b50e19d51ea

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwere added
  2. 2
    workup.STIRRINGstirred at the same temperature for 30 min
  3. 3
    Sonstigethe organic layer was separated
  4. 4
    Extraktionthe aqueous layer was extracted with chloroform
  5. 5
    Waschenwashed sequentially with water and aqueous saturated sodium chloride solution
  6. 6
    Trocknendried over anhydrous magnesium sulfate
  7. 7
    Sonstigethe solvent was removed under reduced pressure
  8. 8
    SonstigeThe residue thus obtained
  9. 9
    Sonstigewas purified by silica gel column chromatography [eluent; chloroform:methanol=5:1]

Vorschrift

To 2 mL of dichloromethane solution containing 77 mg of N-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)-4-methylpiperidine-4-amine, 68 mg of (7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)acetaldehyde and 17 μL of acetic acid were added and stirred at room temperature for 1 hour. To the reaction mixture, 93 mg of sodium triacetoxyborohydride was added and stirred at the same temperature for 30 min. Chloroform and aqueous saturated sodium hydrogen carbonate solution were added, the organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and extracts were combined, washed sequentially with water and aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; chloroform:methanol=5:1] to give 0.13 g of 1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidin-1-yl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-one as a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524738B2uspto-grants-2013_09