Reacción #46268

ord-2854a54fd2fc4c4fb7ea9ef8fbbb375b

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe product mixture was concentrated under vacuum to the title bisacetate
  2. 2
    Otrowas used in the following step without further purification

Procedimiento

A solution of ethyl 6-(3-chloro-4-fluorobenzyl)-4-hydroxy-5-oxo-5,6,7,8-tetrahydro-2,6-naphthyridine-1-carboxylate 2-oxide (23 g, 58 mmol) in acetic anhydride (400 mL) was heated under nitrogen at 100° C. for one hour. The product mixture was concentrated under vacuum to the title bisacetate and was used in the following step without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741315B2uspto-grants-2010_06