Methyl 2-aminopyridine-4-carboxylate → (2-Aminopyridin-4-yl)methanol

HRID 985412

反応式

HRID 985412 の反応式
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) δ 7.79 (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

  1. customdried round bottom flask under nitrogen gas
  2. additionLAH (39.4 mL, 1M in THF) was added slowly
  3. temperatureto warm to 0° C.
  4. customwas quenched by the addition of 15 mL of 1M NaOH (aq)
  5. filtrationThe solution was filtered
  6. washthe solid was washed with THF
  7. concentrationThe filtrate was concentrated
  8. customto afford the pure product

出典と根拠

ORDレコード
ord-7b8b21ff012f4c7daf9cfec6b556f0bb
出典データセット
uspto-grants-2005_03
特許番号
US06872724B2

関連ノート

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