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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 419610Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 1-[2-Chloro-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine

https://huagongshe.com/de/reaction/419610

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktPotassium CarbonateHCID 11430—
Edukt1-Chloro-2-fluoro-4-methoxy-5-nitrobenzeneHCID 53403289—
Edukt1-[2-(Methylsulfonyl)ethyl]piperazine hydrochlorideHCID 66649667—
LösungsmittelWaterHCID 962—
Produkt1-[2-Chloro-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazineHCID 5945263491,3%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To 1-chloro-2-fluoro-4-(methyloxy)-5-nitrobenzene (Example 104, Step B) (0.822 g, 4.0 mmol), 4-[2-(methylsulfonyl)ethyl]piperazine hydrochloride (Example 148, Step B) (0.915 g, 4.0 mmol), and K2CO3 (1.7 g, 12 mmol) was added DMSO (8 mL). The reaction was heated to 100° C. for two days. The reaction was determined to be complete by TLC. The reaction mixture was diluted with H2O and extracted with DCM and EtOAc sequentially for two iterations. The organic was dried (MgSO4), filtered, and rotovapped down. Purification by flash chromatography provided the title compound of Step A (1.38 g, 91%). MS (M+H, ES+) 378.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093239B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-86d4005b11134c4792f37dc014c8d999
Quellennotizuspto-grants-2012_01