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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246546Generated: October 30, 2026

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

https://huagongshe.com/reaction/246546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Chloroimidazo[1,5-A]pyridineHCID 71743998—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Chloro-1-iodoimidazo[1,5-A]pyridineHCID 7127965436%

Reaction Steps

To a solution of 6-chloroimidazo[1,5-a]pyridine (417 mg, 2.73 mmol) in EtOH (5 mL) and water (2.4 mL) was added sodium bicarbonate (861 mg, 10.2 mmol) and iodine (832 mg, 3.28 mmol) and the mixture stirred at room temperature under N2. After 16 h the reaction mixture was quenched with sodium thiosulfate, then extracted into ethyl acetate. The organic layer was washed with water and brine, dried (MgSO4), filtered, and concentrated. Purification of the filtrate by chromatography (silica, 20-60% ethyl acetate/hexanes) gave 6-chloro-1-iodoimidazo[1,5-a]pyridine (271 mg, 973 μmol, 36%) as a brown solid. MS (M+H)+=278.8; 1H NMR (CDCl3) δ: 8.10 (s, 1H), 8.0 (m, 1H), 7.30 (d, J=9.5 Hz, 1H), 6.76 (9.5 m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-bc47ca8f25864824ae7f6f5cf1c79dfb
Source noteuspto-grants-2014_02