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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31812생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/31812

반응식

참여 물질

역할이름HCID투입량
반응물EthylenediamineHCID 3301—
반응물6-Chloro-3-pyridinecarbonitrileHCID 5152094—
용매AcetonitrileHCID 6342—
생성물6-[(2-Aminoethyl)amino]pyridine-3-carbonitrileHCID 1136940578%

반응 조건

온도77.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425557B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-75ea0628dfc5434fb8ce103e8be9f53e
출처 메모uspto-grants-2008_09