Ammonia → 4-amino-6-isopropyl-3-nitro-1H-pyridin-2-one
反応式
Cl[C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[NH:5][C:4](=[O:11])[C:3]=1[N+:12]([O-:14])=[O:13].[NH3:15]>CO>[NH2:15][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[NH:5][C:4](=[O:11])[C:3]=1[N+:12]([O-:14])=[O:13]参加物
4
反応条件
- 温度
- 100 °C
実験手順
A mixture of 4-chloro-6-isopropyl-3-nitro-1H-pyridin-2-one (700 mg, 3.23 mmol) in 6-7 μL of 7 N NH3 in MeOH is stirred at 100° C. in a sealed tube for 1.5 h. After cooling, the reaction mixture is concentrated in vacuo. The residue is suspended in H2O, filtered, washed with H2O, and dried, yielding 4-amino-6-isopropyl-3-nitro-1H-pyridin-2-one. 1H NMR (DMSO-d6, 300 MHz) δ 10.96 (br s, 1H), 8.15 (br s, 2H), 5.70 (d, J=0.9 Hz, 1H), 2.58 (sept, J=6.9 Hz, 1H), 1.11 (d, J=6.9 Hz, 6H) ppm.
後処理
- temperatureAfter cooling
- concentrationthe reaction mixture is concentrated in vacuo
- filtrationfiltered
- washwashed with H2O
- customdried
出典と根拠
- ORDレコード
- ord-bbd5bbb5fbbf45dc84a9a12ef7509ac6
- 出典データセット
- uspto-grants-2010_01
- 特許番号
- US07642267B2
反応ノート
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