Sulfuric Acid → 2-Acetamido-5-nitropyridine

HRID 1241962Notes

Reaction equation

HRID 1241962 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][N:3]=1.OS(O)(=O)=O.[C:16](OC(=O)C)(=[O:18])[CH3:17]>>[N+:8]([C:5]1[CH:6]=[CH:7][C:2]([NH:1][C:16](=[O:18])[CH3:17])=[N:3][CH:4]=1)([O-:10])=[O:9]

Participants

4

Conditions

Temperature
130 °C

Procedure

To a hot solution of 2-amino-5-nitropyridine (1.4 g, 10 mmol) in acetic anhydride (5 mL) at 100° C. was added conc. H2SO4 (0.1 mL). The resulting mixture was heated at 130° C. for 2 h, cooled and partitioned between EtOAc (200 mL) and water (100 mL). The layers were separated and the aqueous layer was washed once with EtOAc (100 mL). The combined organic layers were washed with water (100 mL), saturated aqueous NaHCO3 (100 mL) and then brine (50 mL); dried over anhydrous MgSO4 and concentrated under reduced pressure to afford N-(5-nitropyridin-2-yl)acetamide (1.8 g, 98%), which was used without further purification. 1H-NMR-(CDCl3): δ 9.14 (1H, d), 8.50 (1H, dd), 8.40 (1H, d), 8.23 (1H, br s), 2.29 (3H, s).

Workup

  1. temperaturecooled
  2. custompartitioned between EtOAc (200 mL) and water (100 mL)
  3. customThe layers were separated
  4. washthe aqueous layer was washed once with EtOAc (100 mL)
  5. washThe combined organic layers were washed with water (100 mL), saturated aqueous NaHCO3 (100 mL)
  6. dry with materialdried over anhydrous MgSO4
  7. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-c1d3dd7b5aa24bebb693169b2912fc65
Source dataset
uspto-grants-2006_10
Patent number
US07115640B2

Reaction notes

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