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

HRID 1450152Notes

Reaction equation

HRID 1450152 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

  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-064d6a2749d749b29d013e5e5fe5e18c
Source dataset
uspto-grants-1997_02
Patent number
US05602075

Reaction notes

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