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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 724729Erstellt: 24. Oktober 2026

Acetonitrile → 4-(4-Fluorophenyl)-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1,2,3,6-tetrahydropyridine

https://huagongshe.com/de/reaction/724729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktTriethylamineHCID 8471—
Edukt4-(4-Fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochlorideHCID 197747—
Edukt2,3-dimethyl-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1H-imidazol-3-ium trifluoromethanesulfonateHCID 10872832—
LösungsmittelWaterHCID 962—
Produkt4-(4-Fluorophenyl)-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1,2,3,6-tetrahydropyridineHCID 2187868552%

Reaktionsschritte

A solution of 4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine hydrochloride (150 mg, 700 μmol), 2,3-dimethyl-1-[(2-methyl-1H-imidazol-1-yl)sulfonyl]-1H-imidazol-3-ium trifluoromethanesulfonate (410 mg, 1.05 mmol), acetonitrile (5 mL) and triethylamine (98 μL, 700 μmol) was stirred at 25° C. for 24 h. The reaction was diluted with water and extracted with ethyl acetate three times, dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by preparative LCMS to yield the desired product (117 mg, 52%). MF=C15H16FN3O2S; LCMS found for C15H17FN3O2S(M+H)+: m/z=322.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07141596B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-43b866aa4e534fa891134f373c1754f0
Quellennotizuspto-grants-2006_11