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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007014Generated: October 28, 2026

1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 178462710, compound

https://huagongshe.com/reaction/1007014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
ReactantHCID 178448214HCID 178448214—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
ProductHCID 178462710HCID 17846271087.1%

Reaction Steps

Trans-4-(tributylstannylphenyl)cyclohexyl acetate(0.56 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (0.46 g) -were heated under reflux in the presence of tetrakistriphenylphosphinepalladium(0) (0.06 g) in xylene in nitrogen atmosphere overnight. 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. Then, it was adjusted to pH 10 by a 8N aqueous solution of sodium hydroxide, extracted with ethyl acetate, washed with a 10% aqueous solution of sodium carbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give a mixture (0.44 g) of 1-(4-ethylpiperazin-1-yl)-3-[4-(trans-4-acetoxycyclohexyl)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-c9c8c65be7864034be8acb2c7b20c05e
Source noteuspto-grants-2004_09