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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1723443생성일: 2026년 10월 25일

4-Vinylpyridine → N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamine

https://huagongshe.com/reaction/1723443

반응식

참여 물질

역할이름HCID투입량
반응물4-VinylpyridineHCID 7502—
반응물N-(4-piperidinyl)-2-benzoxazolamineHCID 14575294—
용매1-ButanolHCID 263—
생성물N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamineHCID 1457587062%

반응 단계

A mixture of 3.2 parts of 4-(1-ethenyl)pyridine, 2.1 parts of N-(4-piperidinyl)-2-benzoxazolamine and 80 parts of 1-butanol was stirred and refluxed for 48 hours. The reaction mixture was evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) saturated with ammonia, as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane, yielding 2 parts (62%) of N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamine; mp. 146.9° C. (450).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04861785
출처 데이터셋uspto-grants-1989_08
ORD IDord-5838677f32fb46fd84bcf7fe3a74ba4f
출처 메모uspto-grants-1989_08