Hydrochloric Acid → 2-Chloro-4-methoxypyridin-3-amine

HRID 2396690Notes

Reaction equation

HRID 2396690 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-4-methoxypyridine in 30 mL 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

  1. customat room temperature
  2. extractionthe resulting mixture was extracted with ether (3×200 mL)
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated by evaporation under reduced pressure
  6. customto obtain a light brown solid
  7. customThis solid was purified by column chromatography (17:83 acetone:hexane)

Sources & evidence

ORD record
ord-d184a987b0e74558b7de13abba5109fb
Source dataset
uspto-grants-1996_02
Patent number
US05494887

Reaction notes

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