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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248755Generated: October 25, 2026

1-(5-Isoquinolinylsulfonyl)piperazine → HCID 13116936, compound

https://huagongshe.com/reaction/1248755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Isoquinolinylsulfonyl)piperazineHCID 3545—
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
ReactantChloroform methanolHCID 21584188—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
ProductHCID 13116936HCID 1311693674.1%

Reaction Steps

In 100 ml of ethanol were added 2.77 g of 1-(5-isoquinolinesulfonyl)piperazine, i.e., Compound (35), 1.66 g of anhydrous potassium carbonate and 5.45 g of ethyl bromide, and the reaction was carried out at an external temperature of 70° C. for 24 hours. After the reaction solution was filtered, the filtrate was condensed and the residue was dissolved in 50 ml of chloroform, and the solution was extracted twice with a 2N aqueous hydrochloric acid solution. The aqueous hydrochloric acid layer was rendered alkaline, extracted twice with 50 ml of chloroform, and the chloroform layer extracted was washed with water and dried with anhydrous magnesium sulfate. After the chloroform was distilled therefrom, the residue obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: 2% methanol-chloroform) to give 2.26 g of 1-(5-isoquinolinesulfonyl)-4-ethylpiperazine, i.e., Compound (42) in a yield of 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525589
Source datasetuspto-grants-1985_06
ORD IDord-2257dfdddf1a41f7a102c66b0c1f0f49
Source noteuspto-grants-1985_06