Reaktion #364620

ord-77b6425747e443e78cd0ed0bab50d7f0

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigesolvent was evaporated
  2. 2
    Sonstigethe residue purified by column chromatography (silica gel, hexane/ether=4/1)

Vorschrift

3-(4-chloro-6-fluoro-2-hydroxy-3-methoxyphenyl)-1-methyl-6-trifluoromethyl-2,4(1H, 3H)-pyrimidinedione (0.10 g, 0.27 mmol) was dissolved in dioxane (10 ml) and the solution added with 2-naphthoyl chloride (0.062 g, 0.33 mmol), triethylamine (0.033 g, 0.33 mmol). After stirred for 2 hr, solvent was evaporated and the residue purified by column chromatography (silica gel, hexane/ether=4/1). Yield: 0.12 g, 0.23 mmol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06355799B1uspto-grants-2002_03