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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897975Generated: October 31, 2026

Iodine chloride → 4-Ethyl-5-iodopyridin-2-amine

https://huagongshe.com/reaction/1897975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
Reactant4-Ethylpyridin-2-amineHCID 118425—
ReactantPotassium AcetateHCID 517044—
SolventAcetic AcidHCID 176—
Product4-Ethyl-5-iodopyridin-2-amineHCID 5820057874%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-ethyl-2-aminopyridine (10.0 g, 81.9 mmol) and potassium acetate (8.00 g, 81.9 mmol) were dissolved in 100 mL of acetic acid and heated to 80° C. with continuous stirring. In a separate flask, iodomonochloride (13.2 g, 81.9 mmol) was dissolved in 30 mL of acetic acid and added to the above reaction mixture drop wise. Once the addition was completed, the reaction mixture was heated for an additional 4 h. Progress of the reaction was monitored by gas chromatography and HPLC. When the reaction was completed, the reaction mixture was cooled to room temperature and quenched with an aqueous solution of saturated sodium bisulfite (10 mL). Acetic acid was removed under vacuum and the residue was dissolved in ethyl acetate and neutralized with saturated NaHCO3. The organic layer was separated from the aqueous layer and the solvent was removed under vacuum. The crude was purified by silica gel column chromatography eluting with 25% ethyl acetate/hexanes. 15 g of desired product was obtained (74% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519384B2
Source datasetuspto-grants-2013_08
ORD IDord-a418b6dc4a5c40e49e0fdb6f14dec7e9
Source noteuspto-grants-2013_08