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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38104Generated: October 27, 2026

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

https://huagongshe.com/reaction/38104

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpyridineHCID 7963—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant3-Dibenzylamino-2,6-difluoro-benzoic acid benzyl esterHCID 58477118—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-pyridin-4-yl-ethanoneHCID 5847712050%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524707B2
Source datasetuspto-grants-2013_09
ORD IDord-433b124ba76c40c0a4ec4512096d975c
Source noteuspto-grants-2013_09