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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

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-Chlorophenyl)-1-isopropylpiperidin-4-amineHCID 3017394—
반응물4-(2-Chloro-2-oxoethyl)phenyl ethyl carbonateHCID 20334074—
용매Methyl Isobutyl KetoneHCID 7909—
생성물{4-[2-{(4-Chlorophenyl)[1-(1-methylethyl)-4-piperidinyl]amino}-2-oxoethyl]phenyl} ethyl carbonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04151286
출처 데이터셋uspto-grants-1979_04
ORD IDord-7acd55a6920842008723b3c2389cad6e
출처 메모uspto-grants-1979_04