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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006977Generated: October 30, 2026

1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 22503411, compound

https://huagongshe.com/reaction/1006977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
ReactantHCID 22503540HCID 22503540—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
ProductHCID 22503411HCID 2250341122.5%

Reaction Steps

N-(2-Benzyloxyethyl)-4-tributylstannylbenzamide (1.23 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (0.49 g) were heated under reflux in the presence of tetrakistriphenylphosphinepalladium(0) (0.13 g) in xylene in nitrogen atmosphere for 3 hr. After cooling, the reaction solution was filtered and concentrated. The resulting residue was purified by silica gel column chromatography (chloroform/methanol system). The resulting product was dissolved in ethyl acetate and 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 extract was washed with a 10% aqueous solution of sodium carbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give 1-(4-ethylpiperazin-1-yl)-3-{4-[N-(2-benzyloxyethyl)carbamoyl]phenyl}isoquinoline (0.17 g) as a pale brown viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790844B2
Source datasetuspto-grants-2004_09
ORD IDord-610755ac53dc40228b09f3a96e96eb95
Source noteuspto-grants-2004_09