Reacción #162612

Ecuación de reacción

2,4,6-trichloropyrimidine

3-oxa-8-azabicyclo[3.2.1]octane hydrochloride

Triethylamine

→

title compound

Rendimiento 75.3%

8-(2,6-Dichloropyrimidin-4-yl)-3-oxa-8-azabicyclo[3.2.1]octane

Rendimiento 75.3%

Disolventes

EtOH

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroIn a 250 mL round-bottomed flask was placed
2. 2
   Temperaturato slowly warm to room temperature
3. 3
   Concentraciónwas then concentrated under reduced pressure
4. 4
   workup.DISSOLUTIONThe residue was dissolved in ethyl acetate
5. 5
   Lavadowashed
6. 6
   SecadoThe organic phase was dried over MgSO4
7. 7
   Filtraciónfiltered
8. 8
   Concentraciónconcentrated
9. 9
   workup.ADDITIONThe crude product was added to a silica gel column
10. 10
    Lavadowas eluted with ethyl acetate in hexanes (5-20%)

Procedimiento

In a 250 mL round-bottomed flask was placed 2,4,6-trichloropyrimidine (8, 0.575 mL, 5 mmol) in EtOH (20 mL) to give a colorless solution. 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride (33, 748 mg, 5.00 mmol) was added and the solution was cooled to 0° C. Triethylamine (2.091 mL, 15 mmol) was added slowly and the mixture was allowed to slowly warm to room temperature. The mixture was stirred at room temperature for one hour and was then concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with sat NaHCO3. The organic phase was dried over MgSO4, filtered and concentrated. The crude product was added to a silica gel column and was eluted with ethyl acetate in hexanes (5-20%) to give the title compound (980 mg, 75%) as a white solid.

Fuente