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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31812Erstellt: 26. Oktober 2026

Ethylenediamine → 6-[(2-Aminoethyl)amino]pyridine-3-carbonitrile

https://huagongshe.com/reaction/31812

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylenediamineHCID 3301—
Edukt6-Chloro-3-pyridinecarbonitrileHCID 5152094—
LösungsmittelAcetonitrileHCID 6342—
Produkt6-[(2-Aminoethyl)amino]pyridine-3-carbonitrileHCID 1136940578%

Reaktionsbedingungen

Temperatur77.5 °C

Reaktionsschritte

A mixture of 2-chloro-5-cyanopyridine (0.60 M) in acetonitrile (120 ml) and ethylene diamine (85 ml) were stirred overnight (ca. 16 h) at 75-80° C. under argon. The ethylene diamine was removed under reduced pressure and then dried in vacuo for 2-3 h. The residual solution was basified with 1 M sodium hydroxide solution (˜100 ml). The aqueous solution was saturated with sodium chloride and extracted with a solution of 95% ethyl acetate and 5% methanol (3×150 ml) and with a solution of 95% acetonitrile and 5% methanol (3×150 ml). The organic extracts were combined and extracted with a saturated sodium chloride solution (2×70 ml). The organic layer was dried with sodium sulfate, filtered, and concentrated under reduced pressure. The crude white to tan solid was triturated with ether (2×50 ml) and dried overnight in vacuo resulting in 78% yield of 6-[(2-aminoethyl)amino]pyridine-3-carbonitrile.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425557B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-75ea0628dfc5434fb8ce103e8be9f53e
Quellennotizuspto-grants-2008_09