Reaktion #557865

ord-35c53c94a3d144fb8e07fab2a6f498c0

Lösungsmittel

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe resulting mixture was stirred at the same temperature for 30 minutes
  2. 2
    Einengenconcentrated under reduced pressure
  3. 3
    ExtraktionAfter extraction with ethyl acetate
  4. 4
    Waschenthe organic layer was washed with brine
  5. 5
    TrocknenThe organic layer was dried over anhydrous magnesium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Sonstigethe solvent in the filtrate was evaporated under reduced pressure
  8. 8
    SonstigeThe residue obtained

Vorschrift

1N sodium hydroxide solution (1.8 ml) was added to a methanol (10 ml) solution of the compound (1.00 g, 1.49 mmol) obtained in Step 1 of Example 108 and the resulting mixture was stirred at 70° C. for 5 hours. 65% Aqueous methanol (15 ml) solution of cerium (IV) diammonium nitrate (3.2 g, 5.96 mmol) was added dropwise to the reaction mixture under ice cooling and the resulting mixture was stirred at the same temperature for 30 minutes. Subsequently, the reaction mixture was rendered weakly acidic (pH 4 to 5) by addition of 1N sodium hydroxide solution and then concentrated under reduced pressure. After extraction with ethyl acetate, the organic layer was washed with brine. The organic layer was dried over anhydrous magnesium sulfate and filtered and then the solvent in the filtrate was evaporated under reduced pressure. The residue obtained was solidified by addition of diethyl ether to give 480 mg (65%) of the title compound as a solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08629133B2uspto-grants-2014_01