Reaktion #6367

ord-45efcb5ccf7b442ba9f977b45016c6dc

Reaktionsgleichung

CCOP(=O)(CO[C@@H](CO)COn1cnc2c(OC)nc(N)nc21)OCC
(S)-2-amino-9-[2-(diethoxyphosphorylmethoxy)-3-hydroxypropoxy]-6-methoxypurine
C[Si](C)(C)Br
trimethylsilyl bromide
Nc1nc2c(ncn2OC[C@H](CO)OCP(=O)(O)O)c(=O)[nH]1
title compound
Ausbeute 66.0%
Nc1nc2c(ncn2OC[C@H](CO)OCP(=O)(O)O)c(=O)[nH]1
(S)-9-[3-Hydroxy-2-(phosphonomethoxy)propoxy]guanine
Ausbeute 66.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed under reduced pressure
  2. 2
    SonstigeThe white solid obtained
  3. 3
    Sonstigewas crystallised from hot water

Vorschrift

To a solution of (S)-2-amino-9-[2-(diethoxyphosphorylmethoxy)-3-hydroxypropoxy]-6-methoxypurine (0.56 g, 1.38 mmol) in dry dimethylformamide (5 ml) was added trimethylsilyl bromide (1.82 ml, 13.8 mmol) and the solution stirred at ambient temperature for 3 hours. The solvent was removed under reduced pressure and the residue co-evaporated with acetone/water 1:1 (x2). The white solid obtained was crystallised from hot water to give the title compound as a white solid (0.305 g, 66%). IR:νmax (KBr) 3380, 3320, 3160, 1715, 1645, 1600, 1385, 1185, 1160, 1100, 1060, 1045, 925, 770 cm-1. 1H NMR: δH (D2O+NH3) 3.61 (1H, dd, J=12.1 Hz J=9.9 Hz, CHBP), 3.65-3.75 (2H, m, CHAP, CHBOH), 3.82-3.89 (1H, m, CH), 3.93 (1H, dd, J=12.3 Hz, J=3.6 Hz, CHAOH), 4.46-4.53 (2H, m, NOCH2), 8.03 (1H, s, H-8). Found: C, 32.24; H, 4.16; N, 20.59%. C9H14N5O7P requires: C, 32.24; H, 4.21; N, 20.89%. m/z: (FAB, thioglycerol matrix) 336 (MH+). [α]D25 (0.1M NaOH)+12.8° (c=0.43).

Quelle

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