Reaktion #6370

ord-1700e5b3912a4121a6882d243c1ca8a2

Reaktionsgleichung

CCOP(=O)(CO[C@@H](CO)COn1cnc2c(N)ncnc21)OCC
(S)-9-[2-(diethoxyphosphorylmethoxy)-3-hydroxypropoxy]adenine
C[Si](C)(C)Br
trimethylsilyl bromide
Nc1ncnc2c1ncn2OC[C@H](CO)OCP(=O)(O)O
title compound
Ausbeute 78.3%
Nc1ncnc2c1ncn2OC[C@H](CO)OCP(=O)(O)O
(S)-9-[3-Hydroxy-2-(phosphonomethoxy)propoxy]adenine
Ausbeute 78.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed under reduced pressure
  2. 2
    SonstigeCrystallisation of the residue from water/acetone

Vorschrift

To a solution of (S)-9-[2-(diethoxyphosphorylmethoxy)-3-hydroxypropoxy]adenine (0.09 g, 0.24 mmol) in dry dichloromethane (3 ml) was added trimethylsilyl bromide (0.31 ml, 2.4 mmol) and the solution stirred at ambient temperature for 4 hours. The solvent was removed under reduced pressure and the residue co-evaporated with acetone/water 1:1 (x3). Crystallisation of the residue from water/acetone gave the title compound as a white solid (0.06 g, 78%), mp. 93°-198° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05247085uspto-grants-1993_09