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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452035Generated: October 25, 2026

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

https://huagongshe.com/reaction/1452035

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 numberUS05606061
Source datasetuspto-grants-1997_02
ORD IDord-7df57b28d5884f26b1638b10098d8457
Source noteuspto-grants-1997_02