Dimethyl Sulfoxide → 5-bromo-1-ethyl-1H-pyrimidin-2-one

Temperatur

15 °C

With cooling with ice, potassium carbonate (13.2 g, 95.7 mmol) and ethyl iodide (2.84 mL, 35.6 mmol) were added to a dimethyl sulfoxide (130 mL) solution of 5-bromo-2-hydroxypyrimidine hydrobromide (7.0 g, 27.3 mmol), and stirred at 15° C. for 16 hours. Water was added to the reaction mixture, and extracted three times with ethyl acetate. The organic layer was washed with saturated brine, dried with anhydrous sodium sulfate and then concentrated under reduced pressure. The organic layer was washed with saturated brine, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified through silica gel column chromatography (C-300, hexane/ethyl acetate=1/1) to obtain the entitled compound (3.34 g, 60%) as a colorless solid.

1. extractionextracted three times with ethyl acetate
2. washThe organic layer was washed with saturated brine
3. dry with materialdried with anhydrous sodium sulfate
4. concentrationconcentrated under reduced pressure
5. washThe organic layer was washed with saturated brine
6. dry with materialdried with anhydrous sodium sulfate
7. concentrationconcentrated under reduced pressure
8. customThe residue was purified through silica gel column chromatography (C-300, hexane/ethyl acetate=1/1)

ORD-Eintrag

ord-a0b9003a24f14d40b79f5c9cd6e9718f

Quelldatensatz

uspto-grants-2012_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08158652B2