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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380188Generated: October 25, 2026

Dichloromethane → 1-{3-[4-(4-Chlorobenzyl)piperazin-1-yl]propyl}-3-(4-fluorophenyl)urea dihydrochloride monohydrate

https://huagongshe.com/reaction/1380188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant4-Fluorophenyl isocyanateHCID 70955—
Reactant1-(3-Aminopropyl)-4-(4-chlorobenzyl)piperazine trihydrochlorideHCID 20205739—
SolventTetrahydrofuranHCID 8028—
Product1-{3-[4-(4-Chlorobenzyl)piperazin-1-yl]propyl}-3-(4-fluorophenyl)urea dihydrochloride monohydrateHCID 2020576076%

Reaction Steps

The procedure described in Example 3 was followed, using 1-(3-aminopropyl)-4-(4-chlorobenzyl)piperazine trihydrochloride (3.77 g; 10 mmole), methylene chloride (50 ml), tetrahydrofuran (10 ml), triethylamine (4.2 ml; 30 mmole) and 4-fluorophenyl isocyanate (1.37 g; 10 mmole). Recrystallization from methanol/methylene chloride provided the title compound (3.75 g; 76% yield) as colorless crystals, m.p. 225°-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579947
Source datasetuspto-grants-1986_04
ORD IDord-c0c7d6b6aa0c4e87ad22d1477142284b
Source noteuspto-grants-1986_04