Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842034Generated: November 3, 2026

Iodine → 6-Bromo-2-iodopyridin-3-amine

https://huagongshe.com/reaction/1842034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant6-Bromopyridin-3-amineHCID 642811—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
Product6-Bromo-2-iodopyridin-3-amineHCID 5340117789.2%

Reaction Steps

5.0 g 5-Amino-2-bromopyridine were dissolved in 70 ml ethanol. 9.0 g silver sulfate and 7.33 g iodine were added. The reaction mixture was stirred at room temperature overnight. The solvent was removed in vacuo and the residue diluted with 500 ml ethyl acetate and filtered over a celite pad. The filtrate was washed with 200 ml saturated Na2S203 solution and water, dried over MgSO4 and then the solvent was removed in vacuo to obtain 7.7 g 6-Bromo-2-iodo-pyridin-3-ylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946212B2
Source datasetuspto-grants-2015_02
ORD IDord-0e25cf880a41421cb72b4c3519daac3d
Source noteuspto-grants-2015_02