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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1166316Erstellt: 25. Oktober 2026

2-Chloro-4'-fluoroacetophenone → 2-(4-chlorophenyl)-4-(4-fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole

https://huagongshe.com/reaction/1166316

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-4'-fluoroacetophenoneHCID 120248—
EduktSodium BicarbonateHCID 516892—
Edukt4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—
LösungsmittelIsopropanolHCID 3776—
Produkt2-(4-chlorophenyl)-4-(4-fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazoleHCID 1013731336,3%

Reaktionsbedingungen

Temperatur82.5 °C

Reaktionsschritte

To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (400 mg, 1.29 mmol) and sodium bicarbonate (216 mg, 2.59 mmol) in isopropanol (25 mL), 2-chloro-4′-fluoroacetophenone (670 mg, 3.87 mmol) was added. After heating the reaction mixture at 80-85° C. for 48 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with aqueous sodium bicarbonate and water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product (800 mg) was purified by chromatography (silica gel, hexane/ethyl acetate, 1/1) to give 2-(4-chlorophenyl)-4-(4-fluorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole (200 mg, 36%) as a pale yellow solid: mp (DSC) 180° C. Anal. Calc'd. for C22H16N2SO2FCl: C, 61.90, H, 3.78, N, 6.56, S, 7.51. Found: C, 61.92, H, 3.74, N, 6.43, S, 7.62.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06613789B2
Quelldatensatzuspto-grants-2003_09
ORD IDord-722abbd61d584315843a27cb084c1222
Quellennotizuspto-grants-2003_09