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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1948201생성일: 2026년 10월 25일

Potassium Carbonate → 1-(cyclohexylmethyl)-5-(4-methoxyphenyl)pyridin-2(1H)-one

https://huagongshe.com/reaction/1948201

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Cyclohexane, (bromomethyl)-HCID 137636—
반응물5-(4-Methoxyphenyl)pyridin-2(1H)-oneHCID 20081497—
용매AcetonitrileHCID 6342—
생성물1-(cyclohexylmethyl)-5-(4-methoxyphenyl)pyridin-2(1H)-oneHCID 5896691931.4%

반응 단계

According to Scheme 5 Step 2: To a solution of 5-(4-methoxyphenyl)pyridin-2(1H)-one (1 eq, 0.35 mmol, 70 mg, Example 7 Step 1) in acetonitrile (2 mL) were added K2CO3 (10 eq, 3.50 mmol, 0.48 g) and (bromomethyl)cyclohexane (10 eq, 3.50 mmol, 0.49 mL). The reaction was microwaved for 10 minutes at 180° C. The reaction was allowed to cool. The reaction was then filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography over silica gel (AIT Flashsmart prepacked column 15 g SiO2) using CH2Cl2/AcOEt (80/20, Rf=0.3). The product was further purified by reverse phase C18 column using water/acetonitrile 60/40 to afford 1-(cyclohexylmethyl)-5-(4-methoxyphenyl)pyridin-2(1H)-one (0.11 mmol, 32 mg, 31%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399493B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-f1a033baa6394e649dbefcb8b87bcc82
출처 메모uspto-grants-2013_03