참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Cyclohexane, (bromomethyl)- | HCID 137636 | — |
| 반응물 | 5-(4-Methoxyphenyl)pyridin-2(1H)-one | HCID 20081497 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1-(cyclohexylmethyl)-5-(4-methoxyphenyl)pyridin-2(1H)-one | HCID 58966919 | 31.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08399493B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-f1a033baa6394e649dbefcb8b87bcc82 |
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| 출처 메모 | uspto-grants-2013_03 |
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