反応式
C[O:2][C:3](=O)[C:4]1[CH:9]=[CH:8][N:7]=[C:6]([NH2:10])[CH:5]=1>C1COCC1>[NH2:10][C:6]1[CH:5]=[C:4]([CH2:3][OH:2])[CH:9]=[CH:8][N:7]=1参加物
3
反応条件
- 温度
- -45 °C
実験手順
2-Amino-isonicotinic acid methyl ester (6.0 g, 39.4 mmol) was dissolved in 80 mL anhydrous THF in a flame dried round bottom flask under nitrogen gas. The solution was cooled to −45° C. and LAH (39.4 mL, 1M in THF) was added slowly. The reaction was allowed to warm to 0° C. and was quenched by the addition of 15 mL of 1M NaOH (aq). The solution was filtered and the solid was washed with THF. The filtrate was concentrated to afford the pure product. 1H NMR (DMSO-d6) δ7.79 (d, 1H, J=5.2 Hz), 6.41 (s, 1H), 6.38 (d, 1H, J=5.9 Hz), 5.79 (bs, 2H), 5.19 (t, 2H, J=5.7), 4.35 (d, 2H, J=5.6 Hz).
後処理
- customdried round bottom flask under nitrogen gas
- additionLAH (39.4 mL, 1M in THF) was added slowly
- temperatureto warm to 0° C.
- customwas quenched by the addition of 15 mL of 1M NaOH (aq)
- filtrationThe solution was filtered
- washthe solid was washed with THF
- concentrationThe filtrate was concentrated
- customto afford the pure product
出典と根拠
- ORDレコード
- ord-9b4b3fb202ef4fc1aaf222f06e44f3e4
- 出典データセット
- uspto-grants-2003_07
- 特許番号
- US06586423B2
関連ノート
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