反応式
[NH2:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[CH:6][CH:7]=1.[CH3:9][N:10]1CCCC1=O>>[NH2:1][C:2]1[C:3]([C:9]#[N:10])=[N:4][CH:5]=[CH:6][CH:7]=1参加物
3
反応条件
- 温度
- 185 °C
実験手順
A mixture of 3-Amino-2-chloro-pyridine (5 g) and cuprous cyanide (5 g) in 10 mL of N-Methylpyrrolidone was heated with stirring at 185° C. for 2 h under an atmosphere of nitrogen. The reaction mixture was concentrated in vacuo and concentrated ammonium hydroxide and 10% methanol/methylene chloride were added. The mixture was shaken and filtered, the organic layer separated and the aqueous layer extracted two times with methanol/methylene chloride. The combined organic extracts were dried over magnesium sulfate and the solvent removed in vacuo. The residue was recrystallized from ethyl acetate/hexane to afford 3-Amino-2-cyanopyridine as a tan solid
後処理
- temperaturewas heated
- concentrationThe reaction mixture was concentrated in vacuo and concentrated ammonium hydroxide and 10% methanol/methylene chloride
- additionwere added
- stirringThe mixture was shaken
- filtrationfiltered
- customthe organic layer separated
- extractionthe aqueous layer extracted two times with methanol/methylene chloride
- dry with materialThe combined organic extracts were dried over magnesium sulfate
- customthe solvent removed in vacuo
- customThe residue was recrystallized from ethyl acetate/hexane
出典と根拠
- ORDレコード
- ord-fbffb0a1d8894513b8ee9de8211916be
- 出典データセット
- uspto-grants-1993_05
- 特許番号
- US05212310
関連ノート
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