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

HRID 1355444

반응식

HRID 1355444 반응식
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

참가 물질

3

반응 조건

온도
-45 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-9b4b3fb202ef4fc1aaf222f06e44f3e4
출처 데이터셋
uspto-grants-2003_07
특허 번호
US06586423B2

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