Réaction #684972

ord-866169d0aa594cd2ad7e6027e71e9945

Équation de réaction

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
Rendement 7.2%
CCCCc1ccc(Cc2ncccc2OC)cc1
2-(4-Butylbenzyl)-3-methoxypyridine
Rendement 7.2%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagethe reaction mixture was washed with saturated brine
  2. 2
    Concentrationconcentrated under reduced pressure
  3. 3
    AutreThe residue was purified by silica gel column chromatography

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07897387B2uspto-grants-2011_03