Hydrochloric Acid → 2-Chloro-4-methoxypyridin-3-amine
Reaction equation
[NH2:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9].OO.C(=O)(O)[O-].[Na+].[ClH:17]>>[NH2:1][C:2]1[C:3]([Cl:17])=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9]Participants
5
Procedure
To a solution of 6.4 g (51 mmol) of 3-amino-4methoxypryidine in 30mL of 37 percent aqueous hydrochloric acid was slowly added 7.8 g of 30 percent aqueous hydrogen peroxide at room temperature with stirring. After 30 min this solution was slowly poured into 300 mL of saturated aqueous sodium bicarbonate and the resulting mixture was extracted with ether (3×200 mL). The ethereal extracts were combined, dried over magnesium sulfate, and filtered. The filtrate was concentrated by evaporation under reduced pressure to obtain a light brown solid. This solid was purified by column chromatography (17:83 acetone:hexane) to obtain 6.54 g (81 percent of theory) of the title compound as colorless needles melting at 86°-87° C.
Workup
- customat room temperature
- extractionthe resulting mixture was extracted with ether (3×200 mL)
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated by evaporation under reduced pressure
- customto obtain a light brown solid
- customThis solid was purified by column chromatography (17:83 acetone:hexane)
Sources & evidence
- ORD record
- ord-064d6a2749d749b29d013e5e5fe5e18c
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05602075
Reaction notes
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