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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216409Erstellt: 23. Oktober 2026

Bis(trifluoroacetoxy)iodobenzene → 4-(2,2-dimethylbutyl)-2-[1-hydroxy-2-oxo-2-(4-pyridin-2-ylphenyl)ethyl]-N,N-dimethyl-1H-imidazole-1-sulfonamide

https://huagongshe.com/de/reaction/216409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(trifluoroacetoxy)iodobenzeneHCID 102317—
Edukt4-(2,2-dimethylbutyl)-2-{hydroxy[2-(4-pyridin-2-ylphenyl)-1,3-dithian-2-yl]methyl}-N,N-dimethyl-1H-imidazole-1-sulfonamideHCID 86638515—
LösungsmittelAcetonitrile--water (1/1)HCID 18373917—
Produkt4-(2,2-dimethylbutyl)-2-[1-hydroxy-2-oxo-2-(4-pyridin-2-ylphenyl)ethyl]-N,N-dimethyl-1H-imidazole-1-sulfonamideHCID 68668285—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

[Bis(trifluoroacetoxy)iodo]benzene (184 mg, 0.48 mmol) was added to a 0° C. solution of 4-(2,2-dimethylbutyl)-2-{hydroxy[2-(4-pyridin-2-ylphenyl)-1,3-dithian-2-yl]methyl}-N,N-dimethyl-1H-imidazole-1-sulfonamide (110 mg, 0.20 mmol) in acetonitrile/water (3:1) (4 mL). After stirring at 0° C. until no further reaction (LCMS), the reaction mixture was quenched with saturated aqueous sodium thiosulfate/saturated aqueous sodium bicarbonate (1:1) and extracted with methylene chloride. The combined organic extracts were dried (magnesium sulfate) and concentrated in vacuo to afford 4-(2,2-dimethylbutyl)-2-[1-hydroxy-2-oxo-2-(4-pyridin-2-ylphenyl)ethyl]-N,N-dimethyl-1H-imidazole-1-sulfonamide which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193228B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-bf6df44a5f974b3592aaa97e974ac2d0
Quellennotizuspto-grants-2012_06