2-Aminonicotinic acid → (2-Aminopyridin-3-yl)methanol

To a solution of 2-aminonicotinic acid (20.5 g, 148.1 mmole) in THF was added lithium aluminum hydride (300 mL, 1.0 M in THF) over 30 minutes. The reaction solution was heated to reflux for 18 hrs and then was cooled to room temperature. The reaction was quenched by the sequential dropwise addition of H2O (11.5 mL), 15% NaOH (11.5 mL), and H2O (34.5 mL). The mixture was stirred for 15 min, then was filtered through Celite®, and the filter pad was washed thoroughly with THF followed by 5% CH3OH/CHCl3. The filtrate was concentrated to give the title compound (15.24 g, 83%) as a waxy light yellow solid: MS (ES) m/e 125 (M+H)+.

1. temperatureThe reaction solution was heated
2. temperatureto reflux for 18 hrs
3. customThe reaction was quenched by the sequential dropwise addition of H2O (11.5 mL), 15% NaOH (11.5 mL), and H2O (34.5 mL)
4. filtrationwas filtered through Celite®
5. washthe filter pad was washed thoroughly with THF
6. concentrationThe filtrate was concentrated

ORD record

ord-1f6a6e34ae894d8a84518da5057ce2f8

Source dataset

uspto-grants-2009_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07524843B2