Reacción #68646

ord-2a7c7b4c25c94c59a4daa243e01bfd0c

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroReaction mixture
  2. 2
    Filtraciónfiltered
  3. 3
    ConcentraciónFiltrate concentrated under reduced pressure
  4. 4
    Otropurified by ISCO silica gel chromatography (10-30% EtOAc/Hexanes)

Procedimiento

A round bottom flask under nitrogen environment was charged with 8-chloro-1,5-naphthyridin-3-ol (1.05 g, 5.8 mmol), 22.8 g of PS-Triphenylphosphine (loading: 2.2 mmol/g), 2-methoxyethanol (2.2 mL, 27.9 mmol), and THF (29.1 ml, 5814 mmol)/DCM (58.1 mL). Mixture cooled to 0° C. and to this was added DEAD (1.84 mL) dropwise via syringe. Reaction mixture allowed to stir at room temperature for 16 hours. Diluted with 50 mL of 10% MeOH/dichloromethane and resin bound reagent filtered. Filtrate concentrated under reduced pressure and purified by ISCO silica gel chromatography (10-30% EtOAc/Hexanes) to afford 8-chloro-3-(2-methoxyethoxy)-1,5-naphthyridine (770 mg, 55% yield) as white solid. MS [M+H]=238.9. Calc'd for C11H11ClN2O2=238.67.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524900B2uspto-grants-2013_09