反応式
[F:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][N:3]=1.CC([O-])=O.[K+].[Br:14]Br>CC(O)=O>[Br:14][C:4]1[N:3]=[C:2]([F:1])[C:7]([NH2:8])=[CH:6][CH:5]=1参加物
5
実験手順
A mixture of 2-fluoropyridin-3-amine (44.6 mmol) and KOAc (44.6 mmol) in AcOH was stirred at room temperature for 1 h. The mixture was cooled to 0 C and Br2 (44.6 mmol) was added dropwise. The mixture was stirred at 0° C. for 15 min. The mixture was concentrated and the residue was dissolved in EtOAc/MeOH. The organic solution was washed (sat. NaHCO3, sat. Na2S2O3), dried (Na2SO4) and concentrated. The residue was purified by flash column chromatography (SiO2, 100:0 to 80:20 petroleum ether/EtOAc) to yield the desired product.
後処理
- additionwas added dropwise
- stirringThe mixture was stirred at 0° C. for 15 min
- concentrationThe mixture was concentrated
- dissolutionthe residue was dissolved in EtOAc/MeOH
- washThe organic solution was washed (sat. NaHCO3, sat. Na2S2O3)
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- customThe residue was purified by flash column chromatography (SiO2, 100:0 to 80:20 petroleum ether/EtOAc)
出典と根拠
- ORDレコード
- ord-ebefc4c650fd47febf3c6cbbab7a5010
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09440929B2
関連ノート
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