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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440235Generated: October 26, 2026

Water → Imidazo[1,2-a]pyridin-6-ylmethanol

https://huagongshe.com/reaction/1440235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantImidazo[1,2-a]pyridine-6-carbaldehydeHCID 7164582—
ReactantDichloromethane methanolHCID 21226129—
SolventMethanolHCID 887—
ProductImidazo[1,2-a]pyridin-6-ylmethanolHCID 706053057%

Reaction Steps

0.90 g of the 6-imidazo[1,2-a]pyridinecarbaldehyde prepared in the Preparative Example 5 was dissolved in 20 ml of methanol. The obtained solution was stirred under cooling with ice, followed by the addition of 90 mg of sodium borohydride. The obtained mixture was stirred for 50 minutes, followed by the addition of water. The obtained mixture was extracted with chloroform. The organic phase was dried over anhydrous magnesium sulfate and distilled to remove the solvent. The obtained residue was purified by silica gel column chromatography [solvent: dichloromethane/methanol (30:1 to 10:1) to give 0.52 g of the title compound as a faintly orange-yellow solid (yield: 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498634
Source datasetuspto-grants-1996_03
ORD IDord-41af41c29e0942c9ae91c5ee99e256c0
Source noteuspto-grants-1996_03