5-Pyrimidinamine, 2-(methylthio)- (9CI) → HCID 58026140, compound

Temperature

0 °C

A stirred solution of 2.0 g (14.2 mmol) of 2-methylsulfanylpyrimidin-5-ylamine in 50 mL of dichloromethane and 10 mL of methanol was cooled in an ice bath. 6.08 g (15.6 mmol) of benzyltrimethylammonium tribromide was added in portions over a period of 10 minutes. The mixture was stirred at 0° C. for 15 minutes and then at room temperature for 3 minutes. The mixture was quenched with saturated aqueous sodium bicarbonate solution until the pH was 8. The organic layer separated and was removed. The aqueous layer was extracted with two 200 mL portions of ethyl acetate. The organic layers were combined, washed with water and brine, dried over sodium sulfate, and concentrated in vacuo. The crude mixture was absorbed onto silica gel and chromatographed on silica gel using ethyl acetate-hexanes to afford 150 mg (5%) 4-bromo-2-methylsulfanylpyrimidin-5-ylamine.

1. waitat room temperature for 3 minutes
2. customThe mixture was quenched with saturated aqueous sodium bicarbonate solution until the pH was 8
3. customThe organic layer separated
4. customwas removed
5. extractionThe aqueous layer was extracted with two 200 mL portions of ethyl acetate
6. washwashed with water and brine
7. dry with materialdried over sodium sulfate
8. concentrationconcentrated in vacuo
9. customThe crude mixture was absorbed onto silica gel
10. customchromatographed on silica gel

ORD record

ord-c477c3b8e17a4012859d14fbd79614a4

Source dataset

uspto-grants-2012_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08268859B2