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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130423Erstellt: 24. Oktober 2026

p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]benzenesulfonamide

https://huagongshe.com/reaction/130423

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Bromobenzenesulfonyl chlorideHCID 7396—
Edukt5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroanilineHCID 59007078—
LösungsmittelPyridine methylene chlorideHCID 21875418—
Produkt4-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]benzenesulfonamideHCID 59007090—

Reaktionsschritte

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-chloroaniline (D34) (108 mg, 0.45 mmol) in pyridine:dichloromethane (1:1, 4 ml) was treated with 4-bromobenzenesulfonyl chloride (138 mg, 0.54 mmol). The solution was stirred at room temperature for 2 hours, quenched with methanol and concentrated in vacuo. The residue was applied to a SCX cartridge (Varian bond-elute, 5 g) and washed with methanol and 2M ammonia in methanol. The combined basic fractions were concentrated in vacuo and the resulting residue was purified by column chromatography (FlashMaster) (dichloromethane to 5% methanol:dichloromethane) to afford some pure product. The impure fractions were purified further by MDAP, and combined with the above pure product to afford the title product (D35). MS (ES+) m/e 458/460/462 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381728B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-f07f4d9910774fc9810990896b77eba6
Quellennotizuspto-grants-2008_06