Hydrazine → 1,2-Dihydro-6-nitro-3H-indazol-3-one

HRID 855637Notes

Reaction equation

HRID 855637 reaction equation
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:5]=1F.[NH2:15][NH2:16]>C(O)C>[N+:10]([C:7]1[CH:6]=[C:5]2[C:4]([C:3](=[O:2])[NH:15][NH:16]2)=[CH:9][CH:8]=1)([O-:12])=[O:11]

Participants

4

Procedure

The crude material, 2-fluoro-4-nitro-benzoic acid methyl ester, from above was treated with hydrazine (1.6 mL, 51 mmol) in ethanol under reflux for 14 hrs. After removal of solvent by evaporation, the residue was washed with water. The precipitate product was filtered and dried on the vacuum pump to give the title compound which was used without further purification(4.0 g, 85% for two steps). MS (ES+): m/e=180.1 (M+H), 178.0 (M−H); LC/Method A/1.83 min.

Workup

  1. temperatureunder reflux for 14 hrs
  2. customAfter removal of solvent
  3. customby evaporation
  4. washthe residue was washed with water
  5. filtrationThe precipitate product was filtered
  6. customdried on the vacuum pump

Sources & evidence

ORD record
ord-d064b788bb014970b2a85ae9f1b5d0b2
Source dataset
uspto-grants-2007_08
Patent number
US07262200B2

Reaction notes

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