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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1248755Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1248755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(5-Isoquinolinylsulfonyl)piperazineHCID 3545—
EduktEthyl BromideHCID 6332—
EduktPotassium CarbonateHCID 11430—
EduktChloroform methanolHCID 21584188—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
ProduktHCID 13116936HCID 1311693674,1%

Reaktionsschritte

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%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04525589
Quelldatensatzuspto-grants-1985_06
ORD IDord-2257dfdddf1a41f7a102c66b0c1f0f49
Quellennotizuspto-grants-1985_06