Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630169Generated: October 29, 2026

2-methylimidazo[1,2-a]pyridine-3-carbaldehyde → (2-methylimidazo[1,2-a]pyridin-3-yl)methanol

https://huagongshe.com/reaction/630169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-methylimidazo[1,2-a]pyridine-3-carbaldehydeHCID 2759859—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(2-methylimidazo[1,2-a]pyridin-3-yl)methanolHCID 706053959%

Reaction Steps

To a solution of sodium borohydride (531 mg, 14.0 mmol) in methanol (30 mL) was added a solution of 2-methylimidazo[1,2-a]pyridine-3-carbaldehyde (1.5 g, 9.4 mmol) in methanol (5 mL) at 0° C. The mixture was stirred for 2 hours at room temperature. The solvent was evaporated, water was added, and the mixture was extracted 3 times with ethyl acetate. The organic phase was washed with brine and dried over sodium sulfate. After evaporation of the solvent, {2-methylimidazo[1,2-a]pyridin-3-yl}methanol was obtained (914 mg, 59% yield) and used in the next step without further purification; 1H NMR (400 MHz, DMSO-d6): δ 2.31 (s, 3H), 4.74 (d, J=5.4 Hz, 2H), 5.06 (t, J=5.4 Hz, 1H), 6.86 (dt, J=6.8 Hz, J=1.3 Hz, 1H), 7.16-7.21 (m, 1H), 7.42 (td, J=9.0 Hz, J=1.2 Hz, 1H), 8.28 (td, J=6.8 Hz, J=1.2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315521B2
Source datasetuspto-grants-2016_04
ORD IDord-34962909ff524d07ad1bd1e563a3e00c
Source noteuspto-grants-2016_04