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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1843631Erstellt: 24. Oktober 2026

4-Methylpyridine → 1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-pyridin-4-yl-ethanone

https://huagongshe.com/de/reaction/1843631

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylpyridineHCID 7963—
EduktAmmonium ChlorideHCID 25517—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt3-Dibenzylamino-2,6-difluoro-benzoic acid benzyl esterHCID 58477118—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-pyridin-4-yl-ethanoneHCID 5847712050%

Reaktionsschritte

To 4-methyl-pyridine (806 μL, 8.33 mmol) in anhydrous tetrahydrofuran (35 mL) was added at 0° C. sodium hexamethyldisilazide 1 M in tetrahydrofuran (16.66 mL, 16.66 mmol) and the reaction was stirred for 20 minutes. 3-Dibenzylamino-2,6-difluoro-benzoic acid benzyl ester (3.691 g, 8.33 mmol) was dissolved in tetrahydrofuran (5 mL) and added dropwise to the solution with 4-methyl-pyridine, the reaction was stirred at 0° C. for one hour. The reaction was poured into saturated ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtrate and concentrated under reduced pressure. The crude was purified by silica gel column chromatography eluting with ethyl acetate 30% in hexane to give the title compound (1.775 g, 50%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08946250B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-2c1c7d9b5611406abc6880f3ce0b7553
Quellennotizuspto-grants-2015_02