Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 513063Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/513063

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt5-Amino-2-chloropyridineHCID 79305—
KatalysatorSilver sulfateHCID 159865—
LösungsmittelEthanolHCID 702—
Produkt6-Chloro-2-iodopyridin-3-amineHCID 1840704386,4%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a solution of 6-chloro-pyridin-3-ylamine (10.0 g, 77.8 mmol) in EtOH (150 mL) was added Ag2SO4 (12.1 g, 38.9 mmol) and I2 (23.7 g, 93.4 mmol) at room temperature. The mixture was stirred at 20° C. overnight. The solvent was removed by evaporation under vacuum. Water (100 mL) and EtOAc (200 mL) were added to the residue. The organic layer was separated and the aqueous layer was extracted with EtOAc (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under vacuum to give the crude product, which was purified by column chromatography on silica gel (Petroleum ether/Ethyl acetate 7:1) to give 6-chloro-2-iodo-pyridin-3-ylamine (17.1 g, 86%). 1H NMR (DMSO, 300 MHz) δ 7.16 (d, J=8.4 Hz, 1H), 7.01 (d, J=8.4 Hz, 1H), 5.57 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09102672B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-df791a2e39074c7ca9e7896999ccfcac
Quellennotizuspto-grants-2015_08