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

HRID 1813985Notes

Reaction equation

HRID 1813985 reaction equation
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

Participants

3

Conditions

Temperature
-45 °C

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-6aec99d129a647279ae151ed48334613
Source dataset
uspto-grants-2005_04
Patent number
US06875767B2

Reaction notes

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