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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46903생성일: 2026년 10월 24일

Methyl Isobutyl Ketone → 1-{3-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]propyl}-1,3-dihydro-5-methyl-3-(1-methylethenyl)-2H-benzimidazol-2-one

https://huagongshe.com/ko/reaction/46903

반응식

참여 물질

역할이름HCID투입량
반응물Methyl Isobutyl KetoneHCID 7909—
반응물Sodium CarbonateHCID 10340—
반응물1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 88638—
반응물1-(3-chloropropyl)-1,3-dihydro-5-methyl-3-(1-methylethenyl)-2H-benzimidazol-2-oneHCID 13105622—
용매WaterHCID 962—
생성물1-{3-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]propyl}-1,3-dihydro-5-methyl-3-(1-methylethenyl)-2H-benzimidazol-2-oneHCID 2038554467%

반응 단계

A mixture of 5.3 parts of 1-(3-chloropropyl)-1,3-dihydro-5-methyl-3-(1-methylethenyl)-2H-benzimidazol-2-one, 4.3 parts of 1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one, 6.4 parts of sodium carbonate and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. After cooling, water is added and the layers are separated. The 4-methyl-2-pentanone-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 6 parts (67%) of 1-{3-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]propyl}-1,3-dihydro-5-methyl-3-(1-methylethenyl)-2H-benzimidazol-2-one as an oily residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175129
출처 데이터셋uspto-grants-1979_11
ORD IDord-4c6c7c68ccbb49558b0fa64500c9b111
출처 메모uspto-grants-1979_11