Reacción #575933

ord-d5ae1a691cd04f22a826f262e8510c2d

Ecuación de reacción

[Na+].[OH-]
sodium hydroxide
Cl
hydrochloric acid
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1C=O
5-chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehyde
[BH4-].[Na+]
sodium borohydride
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CO
title compound
Rendimiento 98.7%
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CO
2-(4-Chloro-2-hydroxymethyl-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanone
Rendimiento 98.7%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe methanol removed by evaporation
  2. 2
    ExtracciónThe resulting aqueous suspension was extracted with ethyl acetate
  3. 3
    LavadoThe organic layer was washed with brine
  4. 4
    Secadodried over magnesium sulfate
  5. 5
    Filtraciónfiltered
  6. 6
    Otroevaporated

Procedimiento

To a solution of 5-chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehyde (0.99 g, 2.36 mmol) in dry methanol (25 mL) was added sodium borohydride (0.19 g, 4.92 mmol). After 1 hour the reaction was acidified to pH 2 by the addition of 1N hydrochloric acid. After 5 minutes the reaction was neutralized with 1N sodium hydroxide and the methanol removed by evaporation. The resulting aqueous suspension was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered and evaporated to give the title compound (0.98 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06974817B2uspto-grants-2005_12