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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246548Generated: October 30, 2026

Iodine → 6-Fluoro-1-iodoimidazo[1,5-A]pyridine

https://huagongshe.com/reaction/246548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Fluoroimidazo[1,5-A]pyridineHCID 71744003—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Fluoro-1-iodoimidazo[1,5-A]pyridineHCID 71279825—

Reaction Steps

To a solution of sodium bicarbonate (1.3 g, 15.4 mmol) in water (3.66 mL) was added 6-fluoroimidazo[1,5-a]pyridine (see Example 32, 560 mg, 4.11 mmol) in EtOH (7.31 mL) followed by iodine (1.46 g, 5.76 mmol) at room temperature. After 16 h another 800 mg of iodine was added. After a further 16 h the reaction mixture was quenched with sodium thiosulfate and diluted with ethyl acetate. The organic phase was washed with water and brine then dried (MgSO4), filtered and concentrated in vacuo. Purification by chromatography (silica, ethyl acetate/hexane gradient). The product contained minor impurities and was used without further purification. MS (M+H)+=262.9; 1H NMR (CDCl3) δ: 8.14 (s, 1H), 7.90 (m, 1H), 7.35 (m, 1H), 6.77 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-bcabaadfc7a94575bd9fab0e9ad7a1ee
Source noteuspto-grants-2014_02