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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918640Generated: November 1, 2026

Iodine → 2-Amino-5-chloro-3-iodopyridine

https://huagongshe.com/reaction/1918640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-Amino-5-chloropyridineHCID 66174—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
Product2-Amino-5-chloro-3-iodopyridineHCID 1107601064%

Reaction Steps

Iodine (7.55 g; 29.73 mmol) was added to a mixture of 5-chloropyridin-2-amine (3.00 g; 22.87 mmol) and silver sulphate (9.36 g; 29.73 mmol) in ethanol (150 mL) and the mixture was stirred overnight at room temperature. The mixture was filtered over celite, washed with ethanol, and the filtrate concentrated under reduced pressure. The residue was dissolved in dichloromethane, and the solution was washed with a saturated aqueous solution of sodium thiosulphate. The organic layer was dried over magnesium sulphate, concentrated under reduced pressure and the crude material purified by flash chromatography on silica gel (eluent: 0 to 30% of ethyl acetate in heptane) to give 3.71 g (64%) of 5-chloro-3-iodopyridin-2-amine as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-280f88754a6b4079bcf3bdef7f5322bf
Source noteuspto-grants-2013_12