Réaction #68012

ord-5f873118b5a743369c8e20d0ff654f65

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas added under a nitrogen atmosphere
  2. 2
    workup.STIRRINGthe mixture was stirred at 90° C. for 48 hours
  3. 3
    TempératureThe reaction mixture was cooled to room temperature
  4. 4
    AutreThe organic layer was separated
  5. 5
    Extractionthe aqueous layer was extracted with ethyl acetate
  6. 6
    Lavagethe resultant solution was washed with an aqueous saturated sodium chloride solution
  7. 7
    Séchagedried over anhydrous magnesium sulfate
  8. 8
    Autrethe solvent was removed under reduced pressure
  9. 9
    AutreThe residue thus obtained
  10. 10
    Autrewas purified by silica gel column chromatography [silica gel; Chromatorex-NH, manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=8:1]

Mode opératoire

To 3 mL of an N,N-dimethylformamide solution containing 0.17 g of 8-methylquinolin-2(1H)-one, 0.13 g of 60% sodium hydride was added under a nitrogen atmosphere, and the mixture was stirred at room temperature for 30 minutes. Thereto was added 0.89 g of 2-bromomethyl-1,3-dioxolane, and the mixture was stirred at 90° C. for 48 hours. The reaction mixture was cooled to room temperature, then ethyl acetate and 1 mol/L hydrochloric acid were added thereto. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [silica gel; Chromatorex-NH, manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=8:1] to obtain 0.18 g of a pale yellow oily substance, 1-(1,3-dioxolan-2-ylmethyl)-8-methylquinolin-2(1H)-one.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08524738B2uspto-grants-2013_09