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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280853생성일: 2026년 10월 25일

p-Anisoyl chloride → 1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazine

https://huagongshe.com/reaction/280853

반응식

참여 물질

역할이름HCID투입량
반응물p-Anisoyl chlorideHCID 7477—
반응물TriethylamineHCID 8471—
반응물3-(4-Benzhydryl-1-piperazinyl)-1-propanamineHCID 13767778—
용매ChloroformHCID 6212—
생성물1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazineHCID 1336283449.8%

반응 단계

To a solution of 1-(3-aminopropyl)-4-benzhydrylpiperazine (1.55 g) and triethylamine (0.7 ml) in chloroform (15 ml) was dropwise added p-methoxybenzoyl chloride (0.85 g) at ambient temperature with stirring, which was continued for 20 minutes. The reaction mixture was washed successively with aqueous sodium bicarbonate and water. The organic layer was separated, dried and evaporated in vacuo. The resultant oily product was subjected to column chromatography on silica gel eluting with ethyl acetate. The fractions containing the desired compound were combined and evaporated in vacuo. The residue was crystallized from a mixture of ethyl acetate and hexane to give 1-[3-(4-methoxybenzoylamino)propyl]-4-benzhydrylpiperazine (1.1 g) as white crystals. mp: 126°-128° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04591590
출처 데이터셋uspto-grants-1986_05
ORD IDord-45435e028d2149abb3c42f25079f2be1
출처 메모uspto-grants-1986_05