Bromine → 5-Bromo-2-(methylsulfanyl)pyrimidin-4(3H)-one

A solution of 2-methylsulfanyl-3H-pyrimidin-4-one (36 g, 0.25 mol) in glacial acetic acid (500 mL) was cooled to 0° C. in an ice bath and treated with Br2 (15.6 mL, 0.3 mol). The reaction mixture changed in color from yellow to brown within 0.5 hours, and was allowed to warm to room temperature where it stirred overnight. When all the starting material had been consumed (as indicated by TLC and HPLC UV detection at λ=254 nm), the reaction mixture was slowly poured into a mixture of ice/H2O (2 liters). The resulting white precipitate was collected by vacuum filtration and washed with H2O (200 mL) and Et2O (2×250 mL). The off-white solid was then suspended in anhydrous toluene (250 mL) and concentrated to dryness under reduced pressure in a 60° C. H2O bath. 5-Bromo-2-methylsulfanyl-3H-pyrimidin-4-one was obtained as a white solid (30.4 g, 55% yield).

1. custombrown within 0.5 hours
2. customWhen all the starting material had been consumed (as indicated by TLC and HPLC UV detection at λ=254 nm)
3. additionthe reaction mixture was slowly poured into a mixture of ice/H2O (2 liters)
4. filtrationThe resulting white precipitate was collected by vacuum filtration
5. washwashed with H2O (200 mL) and Et2O (2×250 mL)
6. concentrationconcentrated to dryness under reduced pressure in a 60° C

ORD record

ord-c7cc2127ed264ce9a8ff43fb1032f74c

Source dataset

uspto-grants-2007_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07217794B2