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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 379396Erstellt: 23. Oktober 2026

2-Bromoethanol → N-(3,5-Bis-trifluoromethyl-benzyl)-6-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-N-methyl-4-o-tolyl-nicotinamide

https://huagongshe.com/de/reaction/379396

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromoethanolHCID 10898—
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
EduktN-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamideHCID 10280286—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-(3,5-Bis-trifluoromethyl-benzyl)-6-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-N-methyl-4-o-tolyl-nicotinamideHCID 993818878,7%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

A mixture of 100 mg (0.186 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamide (Example 53), 0.030 ml (0.42 mmol)2-bromo-ethanol and 46 mg (0.33 mmol) potassium carbonate in 2 ml acetonitrile was stirred at 45° C. for 70 h. After cooling to room temperature 10 ml 1 N sodium hydroxide solution were added. Extraction with 3 15-ml portions of ethyl acetate, drying with sodium sulfate and concentration gave 138 mg of the crude product. Flash column chromatography afforded 85 mg (78.6%) of the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06297375B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-911c5194d69542a1ab0ef605ba97880a
Quellennotizuspto-grants-2001_10