Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248757Generated: October 31, 2026

1-(5-Isoquinolinylsulfonyl)piperazine → HCID 13116945, compound

https://huagongshe.com/reaction/1248757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Isoquinolinylsulfonyl)piperazineHCID 3545—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
ProductHCID 13116945HCID 1311694579%

Reaction Steps

In 150 ml of ethanol were added 2.77 g of 1-(5-isoquinolinesulfonyl)piperazine, i.e., Compound (35), 1.0 g of potassium hydroxide and 1.9 g of benzyl chloride, and the mixture was refluxed under heating for five hours. After the ethanol was removed from the reaction solution, 100 ml of chloroform was added to the resulting solution, and the solution obtained was washed with a buffer solution having a pH of 5.5 and extracted twice with 20 ml of 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 under reduced pressure, 5 ml of a 10N aqueous hydrochloric acid solution was added to the residue and the mixture was condensed to dryness. The crystalline residue thus obtained was recrystallized from ethanol to give 2.9 g of 1-(5-isoquinolinesulfonyl)-4-benzylpiperazine [i.e., Compound (56)] dihydrochloride in a yield of 66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525589
Source datasetuspto-grants-1985_06
ORD IDord-58ea52aa69d445779864ee86e92909c3
Source noteuspto-grants-1985_06