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HRID 17448Erstellt: 24. Oktober 2026

Ammonium Chloride → 2-Cyclopropyl-7-fluoro-6-(3-fluorophenyl)-5-methyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/de/reaction/17448

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt3-Fluorophenylboronic acidHCID 2733986—
Edukt6-Bromo-2-cyclopropyl-7-fluoro-5-methylbenzoxazole-4-carbonitrileHCID 51041427—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-Cyclopropyl-7-fluoro-6-(3-fluorophenyl)-5-methyl-1,3-benzoxazole-4-carbonitrileHCID 6858715672%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

6-Bromo-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile (I-77) (200 mg, 0.68 mmol), 3-fluorophenylboronic acid (380 mg, 2.71 mmol) and tripotassium phosphate (288 mg, 1.36 mmol) were dissolved in 1,4-dioxane (8 ml), then at room temperature, tetrakis(triphenylphosphine)palladium(0) (157 mg, 0.14 mmol) was added. The solution was stirred under nitrogen atmosphere at 95° C. for 17 hours. After cooling to room temperature, the reaction liquid was fractionated with ethyl acetate and aqueous saturated ammonium chloride solution. The aqueous layer was further extracted twice with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, hexane:ethyl acetate=8:1) to obtain the entitled compound (151 mg, 72%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737166B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4483e468c3ee43868833523ca3ced70d
Quellennotizuspto-grants-2010_06