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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1987224Erstellt: 26. Oktober 2026

Dimethyl Sulfoxide → N-(4-(((4,4-Difluorocyclohexyl)methyl)amino)-3-nitrophenyl)ethanesulfonamide

https://huagongshe.com/reaction/1987224

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktEthanolamineHCID 700—
EduktN-(4-fluoro-3-nitrophenyl)ethanesulfonamideHCID 3286362—
Edukt1-(4,4-Difluorocyclohexyl)methanamineHCID 15604494—
LösungsmittelWaterHCID 962—
ProduktN-(4-(((4,4-Difluorocyclohexyl)methyl)amino)-3-nitrophenyl)ethanesulfonamideHCID 1151637363,8%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

N-(4-Fluoro-3-nitrophenyl)ethanesulfonamide (26 g, 0.107 mol), [(4,4-difluorocyclohexyl)methyl]amine (approx. 15 g), DIPFA (20 mL) and DMSO (100 mL) were mixed together and heated to 65° C. overnight. Ethanolamine (5 g) was added and the reaction mixture was stirred until complete disappearance of N-(4-fluoro-3-nitrophenyl)ethanesulfonamide (approx. 4-5 hrs.). The room temperature cooled down reaction mixture was poured in cold water (900 mL). The product was extracted with DCM (5×200 mL). The combined organic phases were washed with HCl 2N (3×200 mL) and dried over anhydrous Na2SO4. The solvent was removed and the crude product was purified on silica gel by flash chromatography (this material can be re-crystallized using a mixture of EtOAc and hexane) to provide the title product (24.2 g) as orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07550495B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-98c8825b80c04d309453a53714842663
Quellennotizuspto-grants-2009_06