反応式
[N+:1]([C:4]1[C:5]([NH2:10])=[N:6][CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[I:11](O)(=O)(=O)=O.II>C(O)(=O)C.O.S(=O)(=O)(O)O>[I:11][C:8]1[CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[C:5]([NH2:10])=[N:6][CH:7]=1参加物
反応条件
- 温度
- 90 °C
実験手順
To a solution of 3-nitropyridin-2-amine (1.2 g, 8.63 mmol) in acetic acid (5 ml), water (1 ml) and sulfuric acid (0.2 ml) was added periodic acid (0.4 g, 1.72 mmol, 0.2 eq.) and the mixture was stirred at 90° C. for 15 min. Iodine (0.87 g, 3.45 mmol, 0.4 eq.) was added portionwise and the mixture was heated at 90° C. for 1 h. The mixture was quenched by the addition of water and extracted with ethylacetate (3×150 ml). The combined organic layer was washed with water, aqueous sodium thiosulfate, brine and dried over sodium sulphate. The solvent was distilled off to give the product in 57% yield (1.3 g). 1H NMR (300 MHz, DMSO-d6): δ 8.58 (d, 1H), 8.54 (d, 1H) 8.04 (br s, 2H); LC-MS (ESI); Calculated mass: 265.01: Observed mass: 265.9 [M+H]+ (rt: 1.36 min).
後処理
- temperaturethe mixture was heated at 90° C. for 1 h
- customThe mixture was quenched by the addition of water
- extractionextracted with ethylacetate (3×150 ml)
- washThe combined organic layer was washed with water, aqueous sodium thiosulfate, brine
- dry with materialdried over sodium sulphate
- distillationThe solvent was distilled off
- customto give the product in 57% yield (1.3 g)
- custom265.9 [M+H]+ (rt: 1.36 min)
出典と根拠
- ORDレコード
- ord-f38c30b13fc04fbdbd1db143828f51c7
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447091B2
関連ノート
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