Ethanol → 2-Amino-6-bromo-3-methoxypyridine

HRID 1725671Notes

Reaction equation

HRID 1725671 reaction equation
[Br:1][C:2]1[N:7]=[C:6]([N+:8]([O-])=O)[C:5]([O:11][CH3:12])=[CH:4][CH:3]=1.C(O)C.[Cl-].[NH4+]>[Fe].O>[NH2:8][C:6]1[C:5]([O:11][CH3:12])=[CH:4][CH:3]=[C:2]([Br:1])[N:7]=1

Participants

6

Conditions

Temperature
72.5 °C

Procedure

To a heterogeneous solution of 6-bromo-3-methoxy-2-nitropyridine (32) (2.32 g, 10 mmol) in of ethanol:water (40 mL, each) were added iron powder (2.8 g, 50 mmol), followed by ammonium chloride (2.64 g, 50 mmol) at room temperature. The resulting heterogeneous mixture was then stirred at 70-75° C. for 15 minutes, filtered through celite (when hot), washed with ethanol (2×50 mL) and solvent was then removed under reduced pressure. The residue upon dilution with water afforded a solid, which was isolated by filtration to give 2-amino-6-bromo-3-methoxypyridine (33). LCMS: purity: 95%, MS (m/z): 203 (MH+).

Workup

  1. filtrationfiltered through celite (when hot)
  2. washwashed with ethanol (2×50 mL) and solvent
  3. customwas then removed under reduced pressure
  4. customThe residue upon dilution with water afforded a solid
  5. customwhich was isolated by filtration

Sources & evidence

ORD record
ord-33422c8e1cfc49d2a9d5fbb472b68d3a
Source dataset
uspto-grants-2009_02
Patent number
US07491732B2

Reaction notes

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