Hydrochloric Acid → 3-Bromo-2-methoxypyridin-4-amine
Reaction equation
[Na].[NH2:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5](Cl)[C:4]=1[Br:10].Cl.[CH3:12][OH:13]>>[NH2:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([O:13][CH3:12])[C:4]=1[Br:10]Participants
5
Conditions
- Temperature
- 0 °C
Procedure
Methanol (350 mL) was charged in a two-neck round bottom flask equipped with a guard tube and septum and cooled to 0° C. Sodium metal (23 g) was added to it slowly in pieces. After all sodium metal had dissolved, 4-amino-3-bromo-2-chloro pyridine (23 g, 178 mmol) was added and the solution was heated at 180° C. in a pressure vessel for 5-6 h. The reaction mixture was then cooled to 0° C. and adjusted to pH 8 by addition of conc. HCl. Solvent was removed under reduced pressure and the residue was suspended in ethyl acetate. Undissolved impurities were removed by filtration and the filtrate was concentrated under reduced pressure to obtain pure product.
Workup
- customequipped with a guard tube
- temperaturethe solution was heated at 180° C. in a pressure vessel for 5-6 h
- temperatureThe reaction mixture was then cooled to 0° C.
- customSolvent was removed under reduced pressure
- customwere removed by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- customto obtain pure product
Sources & evidence
- ORD record
- ord-0adb654795fa4864b1e4c80fb0add3f2
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08198448B2
Reaction notes
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