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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404073Generated: October 30, 2026

N-Iodosuccinimide → 3-Iodo-imidazo[1,2-a]pyridine-8-carbonitrile

https://huagongshe.com/reaction/2404073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantImidazo[1,2-a]pyridine-8-carbonitrileHCID 15098893—
SolventDichloromethaneHCID 6344—
Product3-Iodo-imidazo[1,2-a]pyridine-8-carbonitrileHCID 7175726480%

Reaction Steps

To a stirred solution of imidazo[1,2-a]pyridine-8-carbonitrile (1.2 g, 8.38 mmol) in dichloromethane (10 mL) was added N-iodosuccinimide (1.89 g, 8.38 mmol). LCMS monitored the reaction until the starting material consumed completely. The reaction mixture was diluted with dichloromethane and water. The separated organic layer was dried sodium sulfate, filtered and concentrated to give 3-iodoimidazo[1,2-a]pyridine-8-carbonitrile (1.8 g, 6.69 mmol, 80% yield) as a brown solid. MS (ES+) C8H81N3 requires: 269. found: 270 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802697B2
Source datasetuspto-grants-2014_08
ORD IDord-1be97dbdfdfc4a988eb3b3be2dac7368
Source noteuspto-grants-2014_08