Reacción #87402

Ecuación de reacción

5-(4-Bromo-2-methoxyphenyl)-3-methylpyridazine

sodium tert-butoxide

benzophenone imine

Sodium carbonate

NaOAc

ammonium

→

title compound

Rendimiento 93.0%

3-Methoxy-4-(6-methylpyridazin-4-yl)aniline

Rendimiento 93.0%

Disolventes

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe flask was purged with N2 three times
2. 2
   Temperaturacooled down
3. 3
   Filtraciónfiltered through a pad of diatomaceous earth
4. 4
   Lavadothe filter was washed with MTBE
5. 5
   ConcentraciónThe filtrate was concentrated
6. 6
   workup.DISSOLUTIONThe residue was dissolved in MeOH (60 mL)
7. 7
   workup.STIRRINGThe mixture was stirred at room temperature for 1 hour
8. 8
   workup.STIRRINGthe mixture was stirred at room temperature for 10 minutes
9. 9
   Concentraciónconcentrated under reduced pressure
10. 10
    LavadoThe organic phase was washed with water, brine
11. 11
    Secadodried over sodium sulfate
12. 12
    Otrothe solvent was removed under reduced pressure
13. 13
    OtroThe residue was purified by flash chromatography on silica gel
14. 14
    Lavadoeluting with 0% to 1% methanol in ethyl acetate

Procedimiento

5-(4-Bromo-2-methoxyphenyl)-3-methylpyridazine (1.72 g, 6.20 mmol), Pd2(dba)3 (57 mg, 0.062 mmol), BINAP (116 mg, 0.19 mmol), sodium tert-butoxide (833 mg, 8.68 mmol), benzophenone imine (1.25 mL, 7.44 mmol) and toluene (30 mL) were added into a sealed tube. The flask was purged with N2 three times. The reaction was stirred at 80° C. overnight and then cooled down, filtered through a pad of diatomaceous earth and the filter was washed with MTBE. The filtrate was concentrated. The residue was dissolved in MeOH (60 mL). NaOAc (1.22 g, 14.90 mmol) and ammonium hyxroxide hydrochloride (776 mg, 11.2 mmol) was added. The mixture was stirred at room temperature for 1 hour. Sodium carbonate (1.23 g, 11.60 mmol) was added, and the mixture was stirred at room temperature for 10 minutes and then concentrated under reduced pressure. The residue was taken up in dichloromethane. The organic phase was washed with water, brine, dried over sodium sulfate and the solvent was removed under reduced pressure. The residue was purified by flash chromatography on silica gel, eluting with 0% to 1% methanol in ethyl acetate to afford the title compound 1.24 g (93%) as a solid.

Fuente