Reacción #518100

ord-352c2870799141369a15d7023e782ec9

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroReaction
  2. 2
    OtroSolvent was removed nder vacuum
  3. 3
    Lavadoeluted with 10% MeOH in CH2Cl2

Procedimiento

Triethylamine trihydrofluoride (3.91 mL, 24.0mmol) was dissolved in dry THF and triethylamine (1.67 mL, 12 mmol, dry, kept over KOH). This mixture of triethylamine-2HF was then added to 5′-O-tert-butyldiphenylsilyl-2′-O-[N,N-dimethylaminooxyethyl]-5-methyluridine (1.40 g, 2.4 mmol) and stirred at room temperature for 24 hrs. Reaction was monitored by TLC (5% MeOH in CH2Cl2). Solvent was removed nder vacuum and the residue placed on a flash column and eluted with 10% MeOH in CH2Cl2 to get 2′-O-(dimethylaminooxyethyl)-5-methyluridine (766 mg, 92.5%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06656732B1uspto-grants-2003_12