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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814549Generated: October 29, 2026

HCID 22503150, compound → HCID 22503351, compound

https://huagongshe.com/reaction/1814549

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 numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-2d131a5c64ed4ce487cf2e6712616302
Source noteuspto-grants-2005_04