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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400572Generated: October 25, 2026

Iodine → 5-Iodo-2-methylpyridin-4-amine

https://huagongshe.com/reaction/400572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant4-Amino-2-methylpyridineHCID 728670—
SolventWaterHCID 962—
Product5-Iodo-2-methylpyridin-4-amineHCID 5344009711%
Product3-Iodo-2-methylpyridin-4-amineHCID 534852535%

Reaction Steps

A solution of KI (1.96 g, 11.9 mmol) and I2 (1.87 g, 7.36 mmol) in 10 mL of water was added to a refluxing solution of the 2-methylpyridin-4-ylamine (1.00 g, 9.25 mmol) and sodium carbonate (683 mg, 6.44 mmol) in 5 mL of water. The mixture was heated at reflux for 2 hours, cooled to room temperature, and treated with 20 mL of ethyl acetate (EtOAc). Phases were separated and the aqueous layer was extracted with three 20 mL portions of ethyl acetate. The combined organic layers were washed with a saturated aqueous sodium thiosulfate (Na2S2O3) solution, dried over magnesium sulfate, and concentrated in vacuo. Flash chromatography (30% ethyl acetate in hexanes to 100% ethyl acetate, gradient) of the resulting residue yielded 4-amino-3-iodo-6-methylpyridine (first eluting: 226 mg, 11% yield) and 4-amino-3-iodo-2-methylpyridine (second eluting: 116 mg; 5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-1849fb6f36114f8fb9bcbb9b71dc9f02
Source noteuspto-grants-2014_06