Reaktion #60456

Reaktionsgleichung

4-[4-bromo-2-(4,4-dimethylcyclohexyl)phenyl]piperazine-1-carboxylic acid t-butyl ester

cis-2,6-dimethylmorpholine

sodium t-butoxide

tri-t-butylphosphonium tetrafluoroborate

→

title compound

Ausbeute 86.1%

cis-4-[2-(4,4-Dimethylcyclohexyl)-4-(2,6-dimethylmorpholin-4-yl)phenyl]piperazine-1-carboxylic acid t-butyl ester

Ausbeute 86.1%

Lösungsmittel

xylene

Reaktionsbedingungen

Aufarbeitung

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

Vorschrift

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.

Quelle