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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814556Generated: October 31, 2026

1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 22503385, compound

https://huagongshe.com/reaction/1814556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
ReactantHCID 22503653HCID 22503653—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
ProductHCID 22503385HCID 2250338546.7%

Reaction Steps

N-Methyl-N-(2-benzyloxyethyl)-4-tributylstannylbenzamide (1.93 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (0.93 g) were heated under reflux overnight in the presence of tetrakistriphenylphosphinepalladium(0) (0.13 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 and adjusted to pH 10 by a 8N aqueous solution of sodium hydroxide, which was then extracted with ethyl acetate, washed with a 10% aqueous solution of sodium carbonate and brine, and then dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol system), to give 1-(4-ethylpiperazin-1-yl)-3-{4-[N-(2-benzyloxyethyl)-N-methylcarbamoyl]phenyl}isoquinoline (0.69 g) as a pale yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-8c2c02cc7f1f48e6a54dcdb6f36cbece
Source noteuspto-grants-2005_04