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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245853Generated: October 31, 2026

Iodine → (6-Fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol

https://huagongshe.com/reaction/245853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium BicarbonateHCID 516892—
Reactant(6-Fluoro-imidazo[1,5-a]pyridin-3-yl)-methanolHCID 86677906—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(6-Fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanolHCID 7128057050%

Reaction Steps

In a round-bottomed flask, (6-fluoro-imidazo[1,5-a]pyridin-3-yl)-methanol (225 mg, 1.15 mmol) was dissolved in ethanol (2 ml) and water (1 ml). Sodium bicarbonate (341 mg, 4.06 mmol) was added followed by iodine (383 mg, 1.51 mmol). The dark brown suspension was stirred at room temperature for 3 h then quenched with 10% Na2S2O3-solution and extracted with EtOAc (2×). The organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated. The residue was absorbed on silica gel and chromatographed with EtOAc/hexanes (gradient 0-40% EtOAc) to provide 157 mg (50%, 2 steps) of (6-fluoro-1-iodo-imidazo[1,5-a]pyridin-3-yl)-methanol as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-7ec3c0ae825d4f8b96b650a10b4c9233
Source noteuspto-grants-2014_02