Reacción #2116

ord-ed0a8010fe1240b0b02babed64992c40

Ecuación de reacción

CCOCn1cnc2c1c(=O)n(CCCCP(=O)([O-])OCCCc1ccccc1)c(=O)n2C
benzylethyl 4-(7-ethoxymethyl-3-methylxanthin-1-yl)-butylphosphonate
N
ammonia
CCOCn1cnc2c1c(=O)n(CCCCP(=O)([O-])[O-])c(=O)n2C.CC[NH3+].CC[NH3+]
Monoethyl ammonium [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]-phosphonate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe catalyst was filtered off
  2. 2
    Concentraciónthe filtrate was concentrated under reduced pressure
  3. 3
    Otrothe solution obtained
  4. 4
    Otroafter evaporating the solvent
  5. 5
    Otrowas then crystallized from diisopropyl ether

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728686uspto-grants-1998_03