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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251232Generated: November 2, 2026

HCID 22503150, compound → HCID 22503351, compound

https://huagongshe.com/reaction/1251232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22503150HCID 22503150—
ReactantHCID 22503529HCID 22503529—
CatalystHCID 178418397HCID 178418397—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
ProductHCID 22503351HCID 2250335141.4%

Reaction Steps

N-Ethyl-4-tributylstannylbenzenesulfonamide (1.42 g) and 3-bromo-1-(4-formylpiperazin-1-yl)isoquinoline (0.82 g) were heated under reflux in the presence of tetrakistriphenylphosphinepalladium(0) (0.12 g) in xylene in nitrogen atmosphere overnight. After cooling, the reaction solution was diluted with ethyl acetate and filtered. The filtrate was extracted with 5N 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, and the resulting residue was purified by silica gel column chromatography (toluene/acetone system), to give 1-(4-formylpiperazin-1-yl)-3-[4-(N-ethylsulfamoyl)phenyl]isoquinoline (0.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-5d378b94ae8049e8b0f7de3e75dc297a
Source noteuspto-grants-2002_01