Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Vinylpyridine → N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Vinylpyridine | HCID 7502 | — |
| 반응물 | N-(4-piperidinyl)-2-benzoxazolamine | HCID 14575294 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamine | HCID 14575870 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04861785 |
| 출처 데이터셋 | uspto-grants-1989_08 |
| ORD ID | ord-5838677f32fb46fd84bcf7fe3a74ba4f |
| 출처 메모 | uspto-grants-1989_08 |