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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1869263생성일: 2026년 10월 25일

Acetic Acid → 2-(4-Methoxyquinolin-6-yl)-1-(6-methylpyridin-2-yl)ethanone

https://huagongshe.com/reaction/1869263

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-Acetyl-6-methylpyridineHCID 138872—
반응물6-Chloro-4-methoxyquinolineHCID 22288654—
반응물Potassium tert-butoxideHCID 23665647—
촉매palladium(II) acetateHCID 167845—
촉매2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
용매WaterHCID 962—
생성물2-(4-Methoxyquinolin-6-yl)-1-(6-methylpyridin-2-yl)ethanoneHCID 2228865556%

반응 조건

온도70 °C

반응 단계

To a 20 mL threaded pressure tube was added 6-Chloro-4-methoxy-quinoline (298 mg, 1.54 mmol), palladium (II) acetate (7 mg, 0.03 mmol), 2-Dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (a.k.a. AMPHOS, 24 mg, 0.06 mmol), and potassium tert-butoxide (1 M in THF, 3.7 mmol). This mixture was stirred and 1-(6-Methyl-pyridin-2-yl)-ethanone was added. The pressure tube was then sealed and heated to 70° C. The reaction mixture was stirred at 70° C. for 18 hours. LC-MS showed product. The reaction mixture was then cooled and poured into a solution of 600 μL of glacial acetic acid in 30 mL of water. Title compound was extracted with 3×30 mL of chloroform. The organic layers were combined, dried over sodium sulfate, filtered, and concentrated via rotary evaporator. The residue was purified by flash column chromatography (silica gel) using a 1% Methanol/Chloroform solvent system affording 255 mg of desired product (56% yield). HPLC=4.39 min, LC-MS=293 (M+H, mw=292.34).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07638537B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-c99b2267647e420f8fe6a02324bd9ed2
출처 메모uspto-grants-2009_12