Réaction #11946

ord-1a9513f02e8c489b998c3f5654a17c95

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Concentrationthe reaction solution was concentrated
  2. 2
    workup.ADDITION1 mol/l aqueous solution of sodium hydroxide was added
  3. 3
    Extractionfollowed by extraction with chloroform
  4. 4
    LavageThe organic layer was washed with saturated brine
  5. 5
    Séchagedried over anhydrous sodium sulfate
  6. 6
    Concentrationconcentrated
  7. 7
    AutreThe resulting solid was recrystallized from hexane/ethyl acetate
  8. 8
    FiltrationThe deposited crystals were collected by filtration
  9. 9
    Autredried under reduced pressure

Mode opératoire

Commercially available 5-methylpyrazine 2-carboxylic acid (2.05 g) was dissolved in methanol (0.6 ml) and chlorine gas was blown into the solution for 5 minutes. After four hours, the reaction solution was concentrated and 1 mol/l aqueous solution of sodium hydroxide was added, followed by extraction with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The resulting solid was recrystallized from hexane/ethyl acetate. The deposited crystals were collected by filtration and dried under reduced pressure to obtain the title compound (1.44 g) as light brown scale-like crystals.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07098215B2uspto-grants-2006_08