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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274235Generated: October 31, 2026

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

https://huagongshe.com/reaction/2274235

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 numberUS09126951B2
Source datasetuspto-grants-2015_09
ORD IDord-f6ead681766a42f38b2b6a4e69aec252
Source noteuspto-grants-2015_09