Reacción #684972

ord-866169d0aa594cd2ad7e6027e71e9945

Ecuación de reacción

CCOC(C)=O
ethyl acetate
O=C([O-])[O-].[K+].[K+]
Potassium carbonate
CI
methyl iodide
CCCCc1ccc(Cc2ncccc2O)cc1
compound
CCCCc1ccc(Cc2ncccc2O)cc1
2-(4-Butylbenzyl)-3-pyridinol
CCCCc1ccc(Cc2ncccc2OC)cc1
title compound
Rendimiento 7.2%
CCCCc1ccc(Cc2ncccc2OC)cc1
2-(4-Butylbenzyl)-3-methoxypyridine
Rendimiento 7.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadothe reaction mixture was washed with saturated brine
  2. 2
    Concentraciónconcentrated under reduced pressure
  3. 3
    OtroThe residue was purified by silica gel column chromatography

Procedimiento

Potassium carbonate (33.0 mg, 0.239 mmol) and methyl iodide (14.9 μl, 0.239 mmol) were added to a solution of the compound of Example B230 (19.2 mg, 0.0796 mmol) in acetone (1 ml), and this reaction mixture was stirred at room temperature for 3 hours. After ethyl acetate was added, the reaction mixture was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (1.47 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07897387B2uspto-grants-2011_03