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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46917생성일: 2026년 10월 25일

Toluene → 3-acetyl-5-chloro-1-{1-[3-(3-acetyl-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl]-4-piperidinyl}-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/46917

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물DomperidoneHCID 3151—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium CarbonateHCID 10340—
용매WaterHCID 962—
생성물3-acetyl-5-chloro-1-{1-[3-(3-acetyl-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl]-4-piperidinyl}-1,3-dihydro-2H-benzimidazol-2-oneHCID 20385608—

반응 단계

A mixture of 5 parts of 5-chloro-1-{1-[3-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl]-4-piperidinyl}-1,3-dihydro-2H-benzimidazol-2-one, 10 parts of acetic acid anhydride and 90 parts of methylbenzene is stirred and refluxed overnight. The reaction mixture is cooled, water is added and the whole is alkalized with a diluted sodium carbonate solution. The layers are separated and the organic phase is dried, filtered and evaporated. The residue is crystallized from methylbenzene. The product is filtered off and recrystallized from methylbenzene, yielding 4.5 parts of 3-acetyl-5-chloro-1-{1-[3-(3-acetyl-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-propyl]-4-piperidinyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 185.3° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175129
출처 데이터셋uspto-grants-1979_11
ORD IDord-dd1d91501ef243b4bcb45f1720a90f29
출처 메모uspto-grants-1979_11