反応式
[NH2:1][C:2]1[N:7]=[C:6]([C:8](O)=[O:9])[CH:5]=[CH:4][CH:3]=1.B.[OH-].[Na+].[Cl-].[Na+]>O1CCCC1>[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]([CH2:8][OH:9])[N:7]=1参加物
実験手順
A mixture of 6-aminopyridine-2-carboxylic acid (5.0 g.) and a 1.35M solution of borane in tetrahydrofuran (100 ml.) was stirred under argon at reflux for 48 hours. The mixture was cooled and treated with 2N NaOH (50 ml.) and the mixture stirred at room temperature for 18 hours. The aqueous phase was saturated with sodium chloride and the organic phase separated. The aqueous phase was extracted twice with ethyl acetate and the ethyl acetate extracts combined with the tetrahydrofuran solution and the whole evaporated to dryness. The residue was dissolved in ethyl acetate (100 ml.) and the solution washed with saturated aqueous sodium chloride solution (5 ml.) and then dried and evaporated to dryness to give crude 2-amino-6-hydroxymethylpyridine (2.3 g.) which was used without further purification.
後処理
- temperatureat reflux for 48 hours
- temperatureThe mixture was cooled
- customthe organic phase separated
- extractionThe aqueous phase was extracted twice with ethyl acetate
- customthe whole evaporated to dryness
- dissolutionThe residue was dissolved in ethyl acetate (100 ml.)
- washthe solution washed with saturated aqueous sodium chloride solution (5 ml.)
- customdried
- customevaporated to dryness
出典と根拠
- ORDレコード
- ord-a437de3dfd9a4f778480374e6eda580c
- 出典データセット
- uspto-grants-1986_08
- 特許番号
- US04604465
関連ノート
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