Reacción #1869166

Ecuación de reacción

2-chloro-1-[6-(2,5-dimethylpyrrol-1-yl)pyridin-3-yl]ethanone

Water

sodium borohydride

→

2-(2,5-Dimethylpyrrol-1-yl)-5-oxiranylpyridine

Rendimiento 98.0%

Disolventes

tetrahydrofuran

1,4-dioxane

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGthe resulting solution stirred for 45 minutes at room temperature
2. 2
   OtroWhen all the 2-chloro-1-[6-(2,5-dimethylpyrrol-1-yl)pyridin-3-yl]ethanone was consumed the reaction mixture
3. 3
   Temperaturawas cooled to 19° C.
4. 4
   workup.ADDITIONtreated with concentrated HCl (36% w/w) (1.08 L) over 40 minutes
5. 5
   TemperaturaThe mixture was cooled to 11° C.
6. 6
   workup.ADDITIONNaOH (32% w/w) (1.64 L) was added over 45 minutes
7. 7
   Temperaturamaintaining the temperature below 25° C
8. 8
   OtroWhen all the chloroalcohol intermediate was consumed
9. 9
   workup.ADDITIONDCM (5.0 L) and water (5.0 L) were added
10. 10
    workup.STIRRINGthe mixture was stirred
11. 11
    Otroto separate
12. 12
    ExtracciónThe aqueous phase was extracted with DCM (2.50 L)
13. 13
    Lavadothe combined organic phases were washed with water (2×1.0 L)
14. 14
    Concentraciónconcentrated in vacuo

Procedimiento

Water (1.08 Kg) was added dropwise to a suspension of sodium borohydride (0.17 Kg, 4.36 mol) in 1,4-dioxane (6.49 L) at 16° C. and the resulting solution stirred at room temperature. A solution of 2-chloro-1-[6-(2,5-dimethylpyrrol-1-yl)pyridin-3-yl]ethanone (1.08 Kg, 4.35 mol) in tetrahydrofuran (2.16 L) was added over 1 hour and the resulting solution stirred for 45 minutes at room temperature. When all the 2-chloro-1-[6-(2,5-dimethylpyrrol-1-yl)pyridin-3-yl]ethanone was consumed the reaction mixture was cooled to 19° C. and treated with concentrated HCl (36% w/w) (1.08 L) over 40 minutes. The mixture was cooled to 11° C. and NaOH (32% w/w) (1.64 L) was added over 45 minutes maintaining the temperature below 25° C. The mixture was then allowed to granulate at room temperature overnight. When all the chloroalcohol intermediate was consumed, DCM (5.0 L) and water (5.0 L) were added and the mixture was stirred before allowing the phases to separate. The aqueous phase was extracted with DCM (2.50 L) and the combined organic phases were washed with water (2×1.0 L) and concentrated in vacuo. Yield 98% (0.92 Kg) δH (CDCl3, 300 MHz) 2.10 (6H, s), 2.90 (1H, dd), 3.25 (1H, dd), 4.00 (1H, dd), 5.90 (2H, s), 7.20 (1H, d), 7.70 (1H, dd), 8.40 (1H, d) ppm. MS m/z 215 (MH+).

Fuente