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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524091Generated: November 1, 2026

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

https://huagongshe.com/reaction/524091

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+) C8H8IN3 requires: 269. found: 270 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340514B2
Source datasetuspto-grants-2016_05
ORD IDord-62033dadc19e4724b8a6d82ac76bf6b3
Source noteuspto-grants-2016_05