Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007012Generated: October 29, 2026

1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 22503346, compound

https://huagongshe.com/reaction/1007012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
ReactantHCID 69180551HCID 69180551—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
ProductHCID 22503346HCID 2250334694.4%

Reaction Steps

3,4-Bis(acetoxymethyl)tributylstannylbenzene (1.91 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (1.00 g) were heated under reflux overnight in the presence of tetrakistriphenylphosphinepalladium(0) (0.14 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, and the resulting 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 extract 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 (1.36 g) of 1-(4-ethylpiperazin-1-yl)-3-[3,4-bis(acetoxymethyl)phenyl]isoquinoline as a brown viscous oil and the starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790844B2
Source datasetuspto-grants-2004_09
ORD IDord-42b8eabd844b47e68dcb4628bdecaed8
Source noteuspto-grants-2004_09