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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705072Generated: October 30, 2026

N-Iodosuccinimide → 2-Chloro-6-fluoro-3-iodoimidazo[1,2-A]pyridine

https://huagongshe.com/reaction/705072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Chloro-6-fluoroimidazo[1,2-A]pyridineHCID 55267864—
SolventAcetonitrileHCID 6342—
Product2-Chloro-6-fluoro-3-iodoimidazo[1,2-A]pyridineHCID 71743344—

Reaction Steps

To a solution of the title compound from Example 2 Step B (1.0 g, 5.86 mmol) in acetonitrile (29.3 mL) was added N-iodosuccinimide (1.583 g, 7.04 mmol). The resulting mixture was stirred at room temperature for 2 hours, then concentrated under reduced pressure. The resulting residue was diluted with dichloromethane, washed with saturated aqueous sodium chloride solution, dried over MgSO4, filtered, and concentrated under reduced pressure. Purification by flash chromatography on silica gel (10-30% ethyl acetate in hexanes) provided the title compound: LCMS m/z 296.70 [M+H]+, 298.65 [M+2+H]+; 1H NMR (500 MHz, CDCl3) δ 8.03 (t, J=2.8 Hz, 1H), 7.56-7.51 (m, 1H), 7.22-7.18 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173873B2
Source datasetuspto-grants-2015_11
ORD IDord-0875119397c24a428376bd3bfae1ea14
Source noteuspto-grants-2015_11