Réaction #70334

ord-c915df7c41ed40f79bf84532c54bfa1a

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe solvent was removed under reduced pressure
  2. 2
    workup.ADDITION2N aqueous NaOH were added
  3. 3
    AutreThe solvent was removed
  4. 4
    Extractionextracted with CHCl3
  5. 5
    AutreThe crude mixture was purified by ionic exchange through a SCX cartridge
  6. 6
    Autreaffording
  7. 7
    Autre0.060 g (50% of yield)

Mode opératoire

A solution of methyl 2-(6-(benzyloxy)-5-phenylpyridin-3-ylamino)-5-cyclopropylbenzoate (0.34 mmol, 0.155 g) in TFA (1.3 ml) was stirred at 45° C. for 30 minutes. The solvent was removed under reduced pressure. The crude mixture was solved in ethanol (2 ml), 2N aqueous NaOH were added and stirred at room temperature for 16 hours. The solvent was removed and the crude was neutralised with 2N aqueous HCl and extracted with CHCl3. The crude mixture was purified by ionic exchange through a SCX cartridge affording 0.060 g (50% of yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08536165B2uspto-grants-2013_09