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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280853Generated: October 27, 2026

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

https://huagongshe.com/reaction/280853

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
Reactant3-(4-Benzhydryl-1-piperazinyl)-1-propanamineHCID 13767778—
SolventChloroformHCID 6212—
Product1-[3-(4-Methoxybenzoylamino)propyl]-4-benzhydrylpiperazineHCID 1336283449.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591590
Source datasetuspto-grants-1986_05
ORD IDord-45435e028d2149abb3c42f25079f2be1
Source noteuspto-grants-1986_05