Reacción #2505901

Ecuación de reacción

benzyl bromoacetate

3-azido-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one

sodium hydride

→

3-azido-1-benzyloxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one

Disolventes

dimethylformamide

toluene

dimethylformamide

Condiciones de reacción

Tratamiento posterior

1. 1
   Lavadowashed with petroleum ether (3×150 ml)] in dry dimethylformamide (250 ml)
2. 2
   Temperaturathe temperature being maintained at 0°
3. 3
   Temperaturato warm to room temperature
4. 4
   workup.STIRRINGwhile stirring for an additional 18 hours
5. 5
   OtroThe dimethylformamide was removed under reduced pressure
6. 6
   Otrothe residue partitioned between water (500 ml) and dichloromethane (500 ml)
7. 7
   ExtracciónThe aqueous phase was extracted with additional dichloromethane (3×500 ml)
8. 8
   SecadoThe combined extracts were dried over sodium sulfate
9. 9
   Otrothe solvent was removed under reduced pressure
10. 10
    Otroto give the crude ester-azide as an oil
11. 11
    workup.ADDITIONsilica gel (48 g) was added
12. 12
    FiltraciónFiltration and removal of the solvent under reduced pressure

Procedimiento

A solution of 3-azido-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one (8.7 g, 0.043 mol), in dry dimethylformamide (75 ml) was added during 30 min to a stirred suspension of sodium hydride [from a 60% mineral oil dispersion (1.9 g) washed with petroleum ether (3×150 ml)] in dry dimethylformamide (250 ml) maintained at 0° C. under a nitrogen atmosphere. Stirring was continued for an additional 1.5 hours, then benzyl bromoacetate (10.8 g; 0.047 mol) in dry dimethylformamide (75 ml) was added during 45 minutes, the temperature being maintained at 0°. The reaction mixture is then allowed to warm to room temperature while stirring for an additional 18 hours. The dimethylformamide was removed under reduced pressure and the residue partitioned between water (500 ml) and dichloromethane (500 ml). The aqueous phase was extracted with additional dichloromethane (3×500 ml). The combined extracts were dried over sodium sulfate and the solvent was removed under reduced pressure to give the crude ester-azide as an oil. This material was dissolved in toluene (500 ml) and silica gel (48 g) was added. Filtration and removal of the solvent under reduced pressure gave 3-azido-1-benzyloxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, as an oil, used without further purification in the next synthetic step.

Fuente