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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380198Generated: October 31, 2026

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

https://huagongshe.com/reaction/1380198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(3-(4-Chlorophenyl)propyl)piperazineHCID 162873—
Reactant1-(3-Chloropropyl)-3-n-hexylureaHCID 13606732—
SolventDiethyl EtherHCID 3283—
Product1-{3-[4-[3-(4-Chlorophenyl)propyl]piperazin-1-yl]-propyl}-3-n-hexylurea dihydrochlorideHCID 1360672564.5%

Reaction Steps

A mixture of 1-(3-chloropropyl)-3-n-hexylurea (2.21 g; 10 mmole), 1-[3-(4-chlorophenyl)propyl]piperazine (2.39 g; 10 mmole), triethylamine (1.01 g; 10 mmole) and alcohol (25 ml) was refluxed for 18 hours. The cooled reaction mixture was diluted with ether and washed with water, dried (sodium sulfate) and concentrated in vacuo. The resulting yellow viscous oil was purified on a silica gel column (methylene chloride/methanol; 93:7) and precipitated with ethereal hydrochloric acid to provide the title compound (1.6 g; 38% yield) as colorless crystals, m.p. 213°-216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579947
Source datasetuspto-grants-1986_04
ORD IDord-f311854efdbd49e0a98586968b38e346
Source noteuspto-grants-1986_04