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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253566Generated: November 2, 2026

N-Iodosuccinimide → 3-Iodo-5-methoxy-7-phenylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1253566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant5-Methoxy-7-phenylimidazo[1,2-a]pyridineHCID 67206968—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product3-Iodo-5-methoxy-7-phenylimidazo[1,2-a]pyridineHCID 58404858—

Reaction Steps

To a solution of 5-methoxy-7-phenylimidazo[1,2-a]pyridine (397 mg, 1.77 mmol) in acetonitrile (30 ml) was added N-iodosuccinimide (478 mg, 2.12 mmol). After 1 h the reaction mixture was diluted with ethyl acetate, washed with 1N aqueous sodium hydroxide and water, then dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate/isohexane gradient) to give 3-iodo-5-methoxy-7-phenylimidazo[1,2-a]pyridine. 1H NMR (600 MHz, DMSO-d6) δ 7.86 (d, 1H); 7.83 (d, 1H); 7.52-7.53 (m, 1H); 7.48-7.45 (m, 2H); 7.38-7.40 (m, 1H); 7.33-7.35 (m, 1H); 6.61 (d, 1H); 4.10 (s, 3H). LRMS (ESI) calculated for C14H12IN2O [M+H]+, 351.0 found 350.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455477B2
Source datasetuspto-grants-2013_06
ORD IDord-51905adbd323499b890921247fbaaaa6
Source noteuspto-grants-2013_06