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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1843631생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylpyridineHCID 7963—
반응물Ammonium ChlorideHCID 25517—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물3-Dibenzylamino-2,6-difluoro-benzoic acid benzyl esterHCID 58477118—
용매TetrahydrofuranHCID 8028—
생성물1-(3-Dibenzylamino-2,6-difluoro-phenyl)-2-pyridin-4-yl-ethanoneHCID 5847712050%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08946250B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-2c1c7d9b5611406abc6880f3ce0b7553
출처 메모uspto-grants-2015_02