Réaction #2116

ord-ed0a8010fe1240b0b02babed64992c40

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe catalyst was filtered off
  2. 2
    Concentrationthe filtrate was concentrated under reduced pressure
  3. 3
    Autrethe solution obtained
  4. 4
    Autreafter evaporating the solvent
  5. 5
    Autrewas then crystallized from diisopropyl ether

Mode opératoire

6.3 g (0.013 mol) of benzylethyl 4-(7-ethoxymethyl-3-methylxanthin-1-yl)-butylphosphonate were hydrogenated in 100 ml of ethanol over 0.5 g of palladium (10%) on active carbon at room temperature in the course of 4 hours. The catalyst was filtered off, the filtrate was concentrated under reduced pressure, the solution obtained was treated with methanolic ammonia and the residue which remained after evaporating the solvent was then crystallized from diisopropyl ether.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05728686uspto-grants-1998_03