Reaktion #1696829

ord-3d413a960da2449e9e9125e3e9c35e0e

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe mixture was concentrated under reduced pressure to dryness
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in methanol
  3. 3
    Filtrationthe insoluble material was filtered off
  4. 4
    SonstigeThe filtrate was evaporated in vacuo

Vorschrift

To a mixture of 2-chloromethyl-5-benzyloxy-4-pyridone (1.0 g) , tetrahydrofuran (10 ml) and water (10 ml) were added dimethylamine hydrochloride (1.31 g) and sodium hydroxide (0.64 g) . After being stirred for 1.5 hours, the mixture was concentrated under reduced pressure to dryness. The residue was dissolved in methanol and the insoluble material was filtered off. The filtrate was evaporated in vacuo to give 5-benzyloxy-2-(N,N-dimethylamino)methyl-4-pyridone (1.0 g) as a powder.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05401734uspto-grants-1995_03