Reacción #2117

ord-8959e916559b4ac888f77a67d88387d1

Ecuación de reacción

N
ammonia
C[Si](C)(C)Br
trimethylsilyl bromide
CCOCn1cnc2c1c(=O)n(CCCCP(=O)([O-])[O-])c(=O)n2C
[4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate
CO
methanol
CCOCn1cnc2c1c(=O)n(CCCCP(=O)([O-])[O-])c(=O)n2C.[NH4+].[NH4+]
Diammonium [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe dichloromethane was then evaporated
  2. 2
    Otrothe oily residue which remained was dried in a bulb tube in an oil pump vacuum
  3. 3
    Otroto remove excess trimethylsilyl bromide and ethyl bromide
  4. 4
    Otroformed
  5. 5
    workup.STIRRINGstirred at room temperature for 2 hours
  6. 6
    OtroAfter evaporating the solvent
  7. 7
    Otrothe diammonium salt was crystallized from a methanoltdiisopropyl ether mixture

Procedimiento

3.4 ml (0.026 mol) of trimethylsilyl bromide were slowly added dropwise at 0° C., under an argon atmosphere, to a solution of 4.16 g (0.01 mol) of [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate in 5 ml of dichloromethane. The solution was stirred at 0° C. for 1 hour and at room temperature for 2 hours. The dichloromethane was then evaporated and the oily residue which remained was dried in a bulb tube in an oil pump vacuum to remove excess trimethylsilyl bromide and ethyl bromide formed. The residue was taken up in a little methanol and treated with 1 ml of concentrated ammonia solution and stirred at room temperature for 2 hours. After evaporating the solvent, the diammonium salt was crystallized from a methanoltdiisopropyl ether mixture.

Fuente

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