Hydrazine → 1,2-dihydro-6-nitro-3H-indazol-3-one
반응식
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]참가 물질
4
실험 절차
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.
후처리
- temperatureunder reflux for 14 hrs
- customAfter removal of solvent
- customby evaporation
- washthe residue was washed with water
- filtrationThe precipitate product was filtered
- customdried on the vacuum pump
출처 및 근거
- ORD 기록
- ord-d064b788bb014970b2a85ae9f1b5d0b2
- 출처 데이터셋
- uspto-grants-2007_08
- 특허 번호
- US07262200B2
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