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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271139Erstellt: 24. Oktober 2026

1-Methylpiperazine → 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline

https://huagongshe.com/de/reaction/271139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylpiperazineHCID 53167—
Edukt8-Iodo-3-(phenylsulfonyl)quinolineHCID 11406774—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(cyclopenta-2,4-dien-1-yl(phenyl)phosphane);iron(2+)HCID 133083342—
Produkt8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinolineHCID 9929162—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

8-Iodo-3-phenylsulfonyl-quinoline (D6) (190 mg, 0.48 mmol), N-methyl-piperazine (48 mg, 0.48 mmol), sodium tertbutoxide (65 mg, 0.68 mmol), di-palladium tetrakis-(dibenzylidine acetone) [Pd2(dba)3] (88 mg, 0.1 mmol) and 1,1′-diphenylphosphino ferrocene (161 mg, 0.3 mmol) were suspended in degassed dry dioxan (2 ml). The mixture was stirred under argon at 40° C. for 16 hours. The solvent was removed and the residue subjected to flash chromatography on silica gel (eluting with dichloromethane—methanol aq. ammonia) to give the title compound (E1), identical spectroscopically to that prepared by the earlier methods.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452888B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-c336f4147dc6407d896f11bf4a407ad4
Quellennotizuspto-grants-2008_11