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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437622생성일: 2026년 10월 25일

1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one → ethyl 2-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]ethylcarbamate

https://huagongshe.com/reaction/437622

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 88638—
반응물ethyl N-(2-bromoethyl)carbamateHCID 286694—
반응물Sodium BicarbonateHCID 516892—
용매EthanolHCID 702—
생성물ethyl 2-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]ethylcarbamateHCID 21428897—

반응 단계

A mixture of 12.94 parts of ethyl (2-bromoethyl)carbamate, 13.51 parts of 1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one, 10.1 parts of sodium hydrogen carbonate and 160 parts of ethanol is stirred and refluxed overnight. The reaction mixture is cooled, filtered over hyflo and the filtrate is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane, 10% of methanol and one drop of ammonium hydroxide, as eluent. The pure fractions are collected and the eluent is evaporated, yielding 4.4 parts of ethyl 2-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]ethylcarbamate as a residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04031226
출처 데이터셋uspto-grants-1977_06
ORD IDord-73c8c05ebae646fc8d699fc2200a374d
출처 메모uspto-grants-1977_06