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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814586Generated: November 1, 2026

Water → 1-(4-Ethylpiperazin-1-yl)-3-phenacylisoquinoline

https://huagongshe.com/reaction/1814586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetophenoneHCID 7410—
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
ReactantHCID 178418922HCID 178418922—
CatalystMercuryHCID 23931—
SolventDimethyl SulfoxideHCID 679—
Product1-(4-Ethylpiperazin-1-yl)-3-phenacylisoquinolineHCID 2250345189.1%

Reaction Steps

A mixed solution of 1-(4-ethylpiperazin-1-yl)-3-bromoisoquinoline (1.00 g), acetophenone (1.50 g) and tert-butoxypotassium (1.40 g) in dimethyl sulfoxide (50 ml) was irradiated with light (450 W; mercury-vapor lamp) at room temperature for 5 hr. Water (200 ml) was added to the reaction solution, and the mixture was extracted with ethyl acetate. The resulting organic layer was washed with water and brine, and then extracted with a 2N aqueous solution of hydrochloric acid (100 ml). The resulting aqueous layer was basified with sodium carbonate and extracted with ethyl acetate. The ethyl acetate layer was washed with water and brine, and dried over magnesium sulfate. The solvent was removed, to give 1-(4-ethylpiperazin-1-yl)-3-phenacylisoquinoline (1.0 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-01d36832457944b4adbd74ffb3411222
Source noteuspto-grants-2005_04