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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437667생성일: 2026년 10월 25일

Benzene → N-[2-{4-[3-(2-cyanoethyl)-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl]-1-piperidinyl}ethyl]-4-fluorobenzamide

https://huagongshe.com/reaction/437667

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물TriethylamineHCID 8471—
반응물1-(4-Fluorobenzoyl)aziridineHCID 84853—
반응물2,3-dihydro-2-oxo-3-(4-piperidinyl)-1H-benzimidazole-1-propanenitrile hydrochlorideHCID 21428923—
용매MethanolHCID 887—
생성물N-[2-{4-[3-(2-cyanoethyl)-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl]-1-piperidinyl}ethyl]-4-fluorobenzamideHCID 21428991—

반응 단계

A mixture of 1.68 parts of 1-(4-fluorobenzoyl)aziridine, 3.07 parts of 2,3-dihydro-2-oxo-3-(4-piperidinyl)-1H-benzimidazole-1-propanenitrile hydrochloride, 1.65 parts of N,N-diethylethanamine, 10.8 parts of benzene and 1.6 parts of methanol is stirred and refluxed for 1.50 hours. The reaction mixture is cooled and poured onto water. The product is extracted with trichloromethane. The extract is dried, filtered and evaporated. The residue is crystallized from 2-propanol. The product is filtered off and recrystallized from 2-propanol, yielding 1part of N-[2-{4-[3-(2-cyanoethyl)-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl]-1-piperidinyl}ethyl]-4-fluorobenzamide; mp. 172.2° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04031226
출처 데이터셋uspto-grants-1977_06
ORD IDord-d430f8b65d8c48dfbff9d02feace18b1
출처 메모uspto-grants-1977_06