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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1415332생성일: 2026년 10월 27일

Acrylonitrile → 1-(3-Aminopropyl)-4-[2-(1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]-3-pentylamino)ethyl]piperidine

https://huagongshe.com/reaction/1415332

반응식

참여 물질

역할이름HCID투입량
반응물AcrylonitrileHCID 7855—
반응물4-PiperidineethanamineHCID 1512602—
반응물1,5-Di-(3,3-dimethylnorborn-2-yl)-3-pentanoneHCID 21332846—
생성물1-(3-Aminopropyl)-4-[2-(1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]-3-pentylamino)ethyl]piperidineHCID 21483969—

반응 단계

As an alternative to obtaining a mixture of Schiff bases VI and VI(a) or VI(b), the reaction can be conducted stepwise. For example, 4-(2-aminoethyl)piperidine may be converted to a Schiff base with 1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]pentan-3-one, catalytically reduced, the ring nitrogen selectively cyanoethylated with acrylonitrile, followed by catalytic hydrogenation to furnish 1-(3-aminopropyl)-4-[2-(1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]-3-pentylamino)ethyl]piperidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04003934
출처 데이터셋uspto-grants-1977_01
ORD IDord-71023bb448a74992ad683619ac9ef9d1
출처 메모uspto-grants-1977_01