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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916038Generated: October 31, 2026

N-Iodosuccinimide → 2-Ethyl-3-iodoimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1916038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Ethylimidazo[1,2-a]pyridineHCID 21831991—
SolventAcetonitrileHCID 6342—
Product2-Ethyl-3-iodoimidazo[1,2-a]pyridineHCID 130054803—

Reaction Steps

As shown in FIG. 8, N-iodosuccinimide (8.37 g, 57.25 mmol) was added to a solution of 2-ethyl-imidazo[1,2-α]pyridine 70 (Example 27) (12.88 g, 57.25 mmol) in dry acetonitrile (100 mL) at 0° C. The reaction was warmed to room temperature and then stirred for 12 hours. The mixture was then concentrated and purified on silica gel (CombiFlash, Heptane/EtOAc elution) to afford 2-ethyl-3-iodo-imidazo[1,2-α]pyridine 72, as photosensitive yellow crystals with a yield of 5.6 g, 35%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618079B2
Source datasetuspto-grants-2013_12
ORD IDord-577970f1637c4aceaadce2642be712d7
Source noteuspto-grants-2013_12