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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814560Generated: November 1, 2026

Ethyl Acetate → HCID 22503440, compound

https://huagongshe.com/reaction/1814560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
ReactantHCID 22503492HCID 22503492—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
ProductHCID 22503440HCID 22503440—

Reaction Steps

2-(3-Fluoro-4-tributylstannylphenyl)ethyl acetate (2.77 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (1.19 g) were heated under reflux overnight in the presence of tetrakistriphenylphosphinepalladium(0) (0.17 g) in xylene in nitrogen atmosphere. After cooling, the reaction solution was diluted with ethyl acetate and filtered. The filtrate was extracted with 2N hydrochloric acid. The aqueous layer was washed with ethyl acetate, adjusted to pH 10 with a 8N aqueous solution of sodium hydroxide, and then extracted with ethyl acetate. The organic layer was washed with a 10% aqueous solution of sodium carbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give a mixture (1.44 g) of 1-(4-ethylpiperazin-1-yl)-3-[3-fluoro-4-(2-acetoxyethyl)phenyl]isoquinoline as a brown viscous oil and the starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-aef42da6c78347c0aecf83e3c5f74c69
Source noteuspto-grants-2005_04