Reaktion #1254650

ord-ad97199a624f4a19942add03c6b27245

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigepurifying by chromatography on a 10 g silica Mega Bond Elut® column
  2. 2
    Wascheneluting with a gradient
  3. 3
    Temperaturincreasing in polarity from 0 to 2.5% MeOH in dichloromethane

Vorschrift

Using essentially the same procedure as for the intermediate of Example 65, but starting with 3-(3-fluoro-4-(2-methyl-imidazol-1-yl)phenyl)-5(R)-hydroxymethyloxazolidin-2-one (202 mg, 0.69 mmol), and purifying by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 2.5% MeOH in dichloromethane, the title compound was prepared (137 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06617339B1uspto-grants-2003_09