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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247138Generated: November 1, 2026

Iodine → 2-amino-N-(5-chloropyridin-2-yl)-5-iodobenzamide

https://huagongshe.com/reaction/1247138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-amino-N-(5-chloropyridin-2-yl)benzamideHCID 21906381—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
Product2-amino-N-(5-chloropyridin-2-yl)-5-iodobenzamideHCID 2190637732.1%

Reaction Steps

To an ice cold stirring suspension of N-(5-chloropyridin-2-yl)-2-aminobenzamide (1.01 g, 4.09 mmol) in ethanol (80 mL) was added a mixture of iodine (1.04 g, 4.10 mmol) and silver sulfate (1.29 g, 4.09 mmol). The mixture was stirred at room temperature for 3 d and filtered. The filtrate was concentrated, partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic phase was dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude product was purified by chromatography over silica gel, eluting with a step gradient of 5–10% ethyl acetate in dichloromethane. The chromatography product was slurried in isopropanol and filtered to give 0.49 g (32%) of an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129245B2
Source datasetuspto-grants-2006_10
ORD IDord-964dbbf9d765483b91741d676f88b888
Source noteuspto-grants-2006_10