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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130430Erstellt: 25. Oktober 2026

5-Bromothiophene-2-sulfonyl chloride → 5-Bromo-N-{5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]phenyl]-2-thiophenesulfonamide

https://huagongshe.com/reaction/130430

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
Edukt5-(cis-3,5-Dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]anilineHCID 59007092—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Bromo-N-{5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]phenyl]-2-thiophenesulfonamideHCID 59007096—

Reaktionsschritte

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]aniline (D39) (300 mg, 0.96 mmol) in dichloromethane (5 ml) and pyridine (5 ml) was added 5-bromo-2-thiophenesulfonyl chloride (505 mg, 1.93 mmol) and the mixture stirred at room temperature for 4 hours. The mixture was then reduced in vacuo and the residue purified by SCX (eluting with methanol then ammonia 2M in methanol). The appropriate fractions were combined and reduced and the residue purified by trituaration with methanol to afford the title compound (D42). MS (ES+) m/e 536/538 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381728B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-4ecedd6316164cc78f6a55d979f81622
Quellennotizuspto-grants-2008_06