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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391557Generated: October 30, 2026

Iodine → Methyl 6-amino-5-iodopyridine-3-carboxylate

https://huagongshe.com/reaction/391557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethyl 6-aminonicotinateHCID 737487—
ReactantChloroform methanolHCID 21584188—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
ProductMethyl 6-amino-5-iodopyridine-3-carboxylateHCID 1535091362.2%

Reaction Steps

To a solution of iodine (3.55 g, 14.0 mmol) in 100 mL absolute ethanol at room temperature was added silver sulfate (4.37 g, 14.0 mmol) and methyl 6-aminonicotinate (1.52 g, 10.0 mmol). After 42 hours the reaction was filtered to isolate a tan precipitate. The solid was heated with 20% MeOH/CHCl3 then cooled to room temperature, filtered, and rinsed with MeOH and CHCl3. The filtrate was evaporated, dissolved in hot MeOH, filtered to remove brownish impurities, and then crystallized from MeOH to give the title compound as a light tan solid (1.73 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383825B2
Source datasetuspto-grants-2013_02
ORD IDord-57750f342fa042cd87a05a8a05b0a5ec
Source noteuspto-grants-2013_02