HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31812Erstellt: 26. Oktober 2026
Ethylenediamine → 6-[(2-Aminoethyl)amino]pyridine-3-carbonitrile
https://huagongshe.com/reaction/31812
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethylenediamine | HCID 3301 | — |
| Edukt | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 6-[(2-Aminoethyl)amino]pyridine-3-carbonitrile | HCID 11369405 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07425557B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-75ea0628dfc5434fb8ce103e8be9f53e |
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| Quellennotiz | uspto-grants-2008_09 |
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