Reacción #558544
ord-b575a31ab1414004aa794f449f81bb19
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Concentraciónconcentrated in vacuo
- 2Otroazeotroped with toluene
- 3TemperaturaHeating
- 4TemperaturaAfter cooling to room temperature
- 5Otroto destroy excess trimethylaluminum
- 6OtroThe reaction mixture was partitioned between CHCl3 and H2O
- 7ExtracciónThe aqueous layer was extracted with CHCl3 (2×50 mL)
- 8LavadoThe combined organic layers were washed with brine
- 9Secadodried over MgSO4
- 10Concentraciónconcentrated in vacuo
- 11workup.ADDITIONammonium chloride was added (400 mg)
- 12TemperaturaThe reaction was heated at 65° C. for 3 h
- 13Concentraciónthe reaction was concentrated in vacuo
Procedimiento
A solution of 2-iodoadenosine (1 g, 2.5 mmol) and ammonium sulfate (0.033 g, 0.25 mmol) in hexamethyldisilazane (20 mL) was heated overnight at 80° C. The reaction was cooled to room temperature, concentrated in vacuo, and azeotroped with toluene. The residue was taken up in THF (10 mL) and Pd(PPh3)4 (0.144 g, 0.125 mmol) was added. The reaction mixture was heated at 68° C. for 10 minutes before the addition of trimethylaluminum (2.0M in hexanes, 5.0 mL, 5.0 mmol). Heating was continued for 3.5 h. After cooling to room temperature, MeOH was added to destroy excess trimethylaluminum. The reaction mixture was partitioned between CHCl3 and H2O. The aqueous layer was extracted with CHCl3 (2×50 mL). The combined organic layers were washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was taken up in MeOH:H2O (4:1) (25 mL) and ammonium chloride was added (400 mg). The reaction was heated at 65° C. for 3 h. When judged complete by TLC, the reaction was concentrated in vacuo and was subjected to silica gel column chromatography running 2% MeOH:DCM with 0.1% NH4OH to afford 2-methyl adenosine.