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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31756생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물EthylenediamineHCID 3301—
반응물6-Chloro-3-nitropyridin-2-ylamineHCID 2724035—
용매AcetonitrileHCID 6342—
생성물2,6-Diamino-N2-(2-aminoethyl)-5-nitropyridineHCID 2214238099%

반응 조건

온도77.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425557B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-19c2c10d27ee45ba98061d97c15efb86
출처 메모uspto-grants-2008_09