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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258859생성일: 2026년 10월 26일

Potassium Iodide → 1-{4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl}-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/258859

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium CarbonateHCID 10340—
반응물p-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
반응물1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 13360889—
용매WaterHCID 962—
용매Methyl Isobutyl KetoneHCID 7909—
생성물1-{4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl}-1,3-dihydro-2H-benzimidazol-2-oneHCID 5415515830%

반응 단계

A mixture of 4 parts of 1-(4-chlorobutyl)-1,3-dihydro-2H-benzimidazol-2-one, 4 parts of (4-fluorophenyl) (4-piperidinyl) methanone hydrochloride, 10 parts of sodium carbonate, 0.2 parts of potassium iodide and 80 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. After cooling, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The solid residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 2 parts (30%) of 1-{4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl} -1,3-dihydro-2H-benzimidazol-2-one; mp. 176.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04035369
출처 데이터셋uspto-grants-1977_07
ORD IDord-fc9d249e84de44eebf843f8c59c1d2ba
출처 메모uspto-grants-1977_07