Reacción #60456

ord-32eb235c33e24e6992c480b63377a8b3

Disolventes

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was air-cooled to room temperature
  2. 2
    Filtraciónthe insoluble matters were filtered off
  3. 3
    workup.ADDITIONwater was added to the obtained filtrate and extraction
  4. 4
    LavadoThe separated organic layer was washed with water and brine in that order
  5. 5
    Secadodried over anhydrous sodium sulfate
  6. 6
    FiltraciónThe desiccant was filtered off
  7. 7
    Concentraciónthe filtrate was concentrated under reduced pressure
  8. 8
    OtroThe resultant residue was purified by silica gel column chromatography (ethyl acetate/hexane)

Procedimiento

A mixture of the 4-[4-bromo-2-(4,4-dimethylcyclohexyl)phenyl]piperazine-1-carboxylic acid t-butyl ester (700 mg, 1.55 mmol) produced in Example (3e), cis-2,6-dimethylmorpholine (268 mg, 2.33 mmol), sodium t-butoxide (372 mg, 3.88 mmol), palladium(II) acetate (35 mg, 0.155 mmol), tri-t-butylphosphonium tetrafluoroborate (135 mg, 0.465 mmol) and xylene (7 mL) was stirred for 2 hours at an external temperature of 100° C. under a nitrogen atmosphere. The reaction mixture was air-cooled to room temperature, and then the insoluble matters were filtered off, water was added to the obtained filtrate and extraction was performed with ethyl acetate. The separated organic layer was washed with water and brine in that order and then dried over anhydrous sodium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give 648 mg of the title compound as yellow crystals.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07425554B2uspto-grants-2008_09