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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251203Generated: November 3, 2026

Water → 1-(4-Ethylpiperazin-1-yl)3-[4-(1,3-dioxolan-2-ylmethyloxy)phenyl]isoquinoline

https://huagongshe.com/reaction/1251203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
Reactant1-(1-Ethylpiperazin-4-yl)-3-(4-hydroxyphenyl)isoquinolineHCID 135719042—
SolventDimethylformamideHCID 6228—
Product1-(4-Ethylpiperazin-1-yl)3-[4-(1,3-dioxolan-2-ylmethyloxy)phenyl]isoquinolineHCID 22503602—

Reaction Conditions

Temperature90 °C

Reaction Steps

The resulting 1-(4-ethylpiperazin-1-yl)-3-(4-hydroxyphenyl)isoquinoline (0.53 g) was dissolved in N,N-dimethylformamide (5 ml), to which were added potassium carbonate (0.24 g) and 2-bromomethyl-1,3-dioxolane (250 ml), and the mixture was stirred at 90° C. overnight. Water was added to the reaction solution, and then the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol system), to give 0.47 g of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-82a0382509d94ab98c0b9e1ca7143d1e
Source noteuspto-grants-2002_01