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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054270Generated: October 31, 2026

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

https://huagongshe.com/reaction/1054270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHexaneHCID 8058—
Reactant6-Bromopyridin-3-amineHCID 642811—
CatalystSilver sulfateHCID 159865—
SolventEthanolHCID 702—
Product6-Bromo-2-iodopyridin-3-amineHCID 5340117765%

Reaction Steps

To a stirred solution of 6-bromo-pyridin-3-ylamine (10.2 g, 0.0580 mol) and Ag2SO4 (18.1 g, 0.0580 mol) in EtOH (150 mL) was added I2 (7.59 g, 0.0580 mol) and the reaction was allowed to stir overnight. At this time hexane (200 mL) was added and the resultant mixture was filtered through Celite. The solvent was removed in vacuo, dissolved in CHCl3 (200 mL), washed with aqueous saturated Na2S2O3 (100 mL), water (1×100 mL), and dried (Na2SO4). The solvent was concentrated in vacuo and the residue was dissolved in hot EtOAc (100 mL), filtered and treated with hexanes (100 mL). Filtration gave 11.2 g (65%) of 6-bromo-2-iodo-pyridin-3-ylamine as a white crystalline material. 1H-NMR (CDCl3; 400 MHz): δ 7.10 (d, 1H, J=8.2 Hz), 6.74 (d, 1H, J=8.2 Hz), 4.06 (br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394289B2
Source datasetuspto-grants-2016_07
ORD IDord-fd0c5ca986ea4eb584a63892f7ebde11
Source noteuspto-grants-2016_07