6-Amino-3-chloropyridazine → 3-Amino-4-bromo-6-chloropyridazine

3-Amino-6-chloro pyridazine (7.87 g) was dissolved in methanol (115 ml). Sodium bicarbonate (10.2 g) was added and then bromine (3.1 ml) was added dropwise, and the mixture was stirred at room temperature for 16 hours. The reaction solution was filtered and then diluted with water (500 ml), and the aqueous layer was extracted with ethyl acetate three times. The organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (developed with ethyl acetate-hexane) to give the title compound (5.2 g) as a brown solid.

1. filtrationThe reaction solution was filtered
2. additiondiluted with water (500 ml)
3. extractionthe aqueous layer was extracted with ethyl acetate three times
4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
5. customThe solvent was evaporated under reduced pressure
6. customThe resulting residue was purified by silica gel column chromatography (developed with ethyl acetate-hexane)

ORD record

ord-3df3524dd04844c296dc0688d99f8889

Source dataset

uspto-grants-2014_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08785438B2