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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916035Generated: November 1, 2026

N-Iodosuccinimide → 8-(Benzyloxy)-3-iodoimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1916035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant8-(Benzyloxy)imidazo[1,2-a]pyridineHCID 13432974—
SolventAcetonitrileHCID 6342—
Product8-(Benzyloxy)-3-iodoimidazo[1,2-a]pyridineHCID 57355243—

Reaction Steps

As shown in FIG. 6, N-iodosuccinimide (7.0 g, 31.2 mmol) was added to a solution of 8-benzyloxy-imidazo[1,2-α]pyridine (Example 19) 24 (7.0 g, 31.2 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 filtered and the cake washed with acetonitrile and water and dried under high vacuum to afford 8-benzyloxy-3-iodo-imidazo[1,2-α]pyridine 31 as colorless solid. 9.0 g, 83%, yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618079B2
Source datasetuspto-grants-2013_12
ORD IDord-84648b43d76f481d941e1350468789d4
Source noteuspto-grants-2013_12