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A 2-L flask fitted with a dry ice condenser and addition funnel was charged with dimethylsulfoxide (500 mL) and a 0.5 M solution of sulfuric acid in dimethylsulfoxide (400 mL), followed by the addition of 2-aminopyrimidine (20.0 g, 211 mmol). The reaction mixture was stirred vigorously for 5 minutes, and then a 1 M solution of iron(II) sulfate in water (60 mL) was added. Trifluoromethyl iodide (200 g, 1.02 moles) was added below the surface of the reaction mixture at room temperature. The reaction mixture was then cooled to 0° C., and 50% aqueous hydrogen peroxide (20 mL, 294 mmol) was added dropwise over one hour. The ice bath was then removed, and the reaction mixture was allowed to warm to room temperature over three hours. The reaction mixture was then carefully neutralized to pH 6.5 with aqueous sodium carbonate. The reaction mixture was then extracted with ethyl acetate (3×300 mL), and the combined organic extracts were dried over magnesium sulfate and concentrated under reduced pressure. The resulting oil was purified by chromatography on silica gel eluting with a hexane/ethyl acetate gradient to afford 4.51 g of the title compound as an off white solid. 1H NMR (CDCl3) δ 8.51 (s, 2H), 5.55 (br s, 2H).

1. customA 2-L flask fitted with a dry ice condenser and addition funnel
2. customThe ice bath was then removed
3. temperatureto warm to room temperature over three hours
4. extractionThe reaction mixture was then extracted with ethyl acetate (3×300 mL)
5. dry with materialthe combined organic extracts were dried over magnesium sulfate
6. concentrationconcentrated under reduced pressure
7. customThe resulting oil was purified by chromatography on silica gel eluting with a hexane/ethyl acetate gradient