Reacción #10537

ord-5ad4245a898440bbbc97f5b29c144228

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroSolvent was removed under reduced pressure
  2. 2
    workup.ADDITIONthe residue taken up in a mixture of dichloromethane:methanol (95:5, by volume, 60 ml)
  3. 3
    FiltraciónInorganic salts were filtered off
  4. 4
    Otrothe filtrate evaporated under reduced pressure
  5. 5
    OtroThe residue was triturated with diethyl ether
  6. 6
    Filtraciónfiltered off
  7. 7
    Otrodried

Procedimiento

A solution of methyl 9-{(2R,3R,4R,5S)-3,4-bis(benzoyloxy)-5-[(ethylamino)carbonyl]-tetrahydro-2-furanyl}-6-[(2,2-diphenylethyl)amino]-9H-purine-2-carboxylate (Preparation 8) (3.4 g, 4.5 mmol) and sodium carbonate (50 mg) in dry methanol (60 ml) was stirred at room temperature for four hours. Solvent was removed under reduced pressure and the residue taken up in a mixture of dichloromethane:methanol (95:5, by volume, 60 ml). Inorganic salts were filtered off and the filtrate evaporated under reduced pressure. The residue was triturated with diethyl ether, filtered off and dried to yield the title compound as a white solid, (2.4 g, 98%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07094769B2uspto-grants-2006_08