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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31756Erstellt: 24. Oktober 2026

Ethylenediamine → 2,6-Diamino-N2-(2-aminoethyl)-5-nitropyridine

https://huagongshe.com/de/reaction/31756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylenediamineHCID 3301—
Edukt6-Chloro-3-nitropyridin-2-ylamineHCID 2724035—
LösungsmittelAcetonitrileHCID 6342—
Produkt2,6-Diamino-N2-(2-aminoethyl)-5-nitropyridineHCID 2214238099%

Reaktionsbedingungen

Temperatur77.5 °C

Reaktionsschritte

A mixture of 2-amino-6-chloro-3-nitropyridine (0.52 M) in acetonitrile (70 ml), and ethylene diamine (40 ml) were stirred overnight (ca. 20 h) at 75-80° C. under argon. The ethylene diamine was removed under reduced pressure. The residual solution was basified with 1M sodium hydroxide solution (50 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 (2×75 ml). The organic layer was dried with sodium sulfate, filtered, and concentrated under reduced pressure. The crude yellow solid was triturated with ether (2×25 ml) and dried overnight in vacuo resulting in 2-(2-aminoethyl)amino-6-amino-5-nitropyridine in 99% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425557B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-19c2c10d27ee45ba98061d97c15efb86
Quellennotizuspto-grants-2008_09