Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26772생성일: 2026년 10월 25일
N-(4-Chlorophenyl)-1-isopropylpiperidin-4-amine → {4-[2-{(4-Chlorophenyl)[1-(1-methylethyl)-4-piperidinyl]amino}-2-oxoethyl]phenyl} ethyl carbonate
https://huagongshe.com/reaction/26772
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-(4-Chlorophenyl)-1-isopropylpiperidin-4-amine | HCID 3017394 | — |
| 반응물 | 4-(2-Chloro-2-oxoethyl)phenyl ethyl carbonate | HCID 20334074 | — |
| 용매 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 생성물 | {4-[2-{(4-Chlorophenyl)[1-(1-methylethyl)-4-piperidinyl]amino}-2-oxoethyl]phenyl} ethyl carbonate | HCID 54328184 | — |
반응 단계
To a stirred mixture of 7.5 parts of N-(4-chlorophenyl)-1-(1-methylethyl)-4-piperidinamine and 80 parts of 4-methyl-2-pentanone are added dropwise 9 parts of [4-(2-chloro-2-oxoethyl)-phenyl] ethyl carbonate. Upon completion, the whole is heated to reflux and stirring is continued for one hour at reflux temperature. After cooling, the precipitated product is filtered off and stirred for 30 minutes in a mixture of alkaline water and trichloromethane. The layers are separated. The organic phase is dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated yielding 5.5 parts of {4-[2-{(4-chlorophenyl)-[1-(1-methylethyl)-4-piperidinyl]amino }-2-oxoethyl]phenyl} ethyl carbonate as an oily residue.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04151286 |
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| 출처 데이터셋 | uspto-grants-1979_04 |
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| ORD ID | ord-7acd55a6920842008723b3c2389cad6e |
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| 출처 메모 | uspto-grants-1979_04 |
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