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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766712Generated: November 1, 2026

N-Iodosuccinimide → 3-[1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-5-iodopyridin-2-amine

https://huagongshe.com/reaction/1766712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant3-(1-(2,6-Dichloro-3-fluorophenyl)ethoxy)pyridin-2-amineHCID 21111396—
SolventAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
Product3-[1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-5-iodopyridin-2-amineHCID 2111139550.1%

Reaction Steps

To a solution of 3-[1-(2,6-Dichloro-3-fluoro-phenyl)-ethoxy]-pyridin-2-ylamine (10.0 g, 33.2 mmol) in acetonitrile (600 mL) and acetic acid (120 mL) was added N-iodosuccinimide (11.2 g, 49.8 mmol). The mixture was stirred at room temperature for 4 hr and the reaction was quenched with Na2S2O5 solution. After evaporation, the residue was partitioned between ethyl acetate and water. The organic layer was washed with 2N NaOH solution, brine, and dried over Na2SO4. The crude product was purified on a silica gel column to provide 3-[1-(2,6-dichloro-3-fluoro-phenyl)-ethoxy]-5-iodo-pyridin-2-ylamine (7.1 g, 50% yield). MS m/z 427 [M+1]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230098B2
Source datasetuspto-grants-2007_06
ORD IDord-6fd82f459286474f92d7c7d1a70d7afb
Source noteuspto-grants-2007_06