Reacción #1702076
ord-35d9f80dfc074e46bceecf40ee635e71
Ecuación de reacción
sodium bicarbonate
5-cyclopropyl-8-methoxy-2,3,5,6-tetrahydrobenzo[b][1,5]diazocin-4(1H)-one
magnesium trifluoromethanesulfonate
2-(phenoxymethyl)oxirane
→
desired compound
Rendimiento 65.0%
5-cyclopropyl-1-(2-hydroxy-3-phenoxypropyl)-8-methoxy-2,3,5,6-tetrahydrobenzo[b][1,5]diazocin-4(1H)-one
Rendimiento 65.0%
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
75°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1TemperaturaAfter cooling to room temperature
- 2Extracciónthe mixture was extracted with dichloromethane
- 3FiltraciónThe organic phases were filtered through a pad of sodium sulfate
- 4Otrothe filtrate evaporated
Procedimiento
To a mixture of 5-cyclopropyl-8-methoxy-2,3,5,6-tetrahydrobenzo[b][1,5]diazocin-4(1H)-one (50.0 mg, 0.203 mmol) from Example 1 and magnesium trifluoromethanesulfonate (32.7 mg, 0.102 mmol) in acetonitrile (1.5 ml) was added 2-(phenoxymethyl)oxirane (30.5 mg, 0.203 mmol) and the resulting mixture was stirred at 75° C. for 100 hours. After cooling to room temperature was added sodium bicarbonate (saturated aqueous) and the mixture was extracted with dichloromethane. The organic phases were filtered through a pad of sodium sulfate and the filtrate evaporated. Preparative thin layer chromatography (EtOAc/MeOH: 95/5) of the obtained residue, gave the desired compound as a brown oil (52 mg, 65%).