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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380200Generated: October 31, 2026

Triethylamine → 1-{3-[4-(3-Trifluoromethyl-4-chlorobenzyl)piperazin-1-yl]propyl}-3-n-hexylurea dihydrochloride

https://huagongshe.com/reaction/1380200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-4-(chloromethyl)-2-(trifluoromethyl)benzeneHCID 13094262—
Reactant1-(3-Piperazinylpropyl)-3-n-hexylureaHCID 57143247—
SolventEthanolHCID 702—
Product1-{3-[4-(3-Trifluoromethyl-4-chlorobenzyl)piperazin-1-yl]propyl}-3-n-hexylurea dihydrochlorideHCID 13606727115.7%

Reaction Steps

A mixture of 1-(3-piperazinylpropyl)-3-n-hexylurea (2.7 g; 10 mmole), 3-trifluoromethyl-4-chlorobenzyl chloride (2.29 g; 10 mmole), triethylamine (1.01 g; 10 mmole) and ethanol (30 ml) was refluxed for 3 hours. The solvent was evaporated in vacuo, and water was added to the residue. The product was extracted with ether, and the extract was dried (sodium sulfate) and concentrated. Precipitation of the oily residue with ethereal hydrochloric acid, followed by recrystallization from alcohol, provided the title compound (3.1 g; 58% yield) as colorless crystals, m.p. 216°-219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579947
Source datasetuspto-grants-1986_04
ORD IDord-56a0a072e0ef45ae8de7ebd0a2ffb280
Source noteuspto-grants-1986_04