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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38104Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/38104

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
PatentnummerUS08524707B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-433b124ba76c40c0a4ec4512096d975c
Quellennotizuspto-grants-2013_09