참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 2-Acetyl-6-methylpyridine | HCID 138872 | — |
| 반응물 | 6-Chloro-4-methoxyquinoline | HCID 22288654 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 촉매 | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(4-Methoxyquinolin-6-yl)-1-(6-methylpyridin-2-yl)ethanone | HCID 22288655 | 56% |
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 (1M in TH, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06958354B2 |
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| 출처 데이터셋 | uspto-grants-2005_10 |
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| ORD ID | ord-be9f08471873469c8098d3f698331953 |
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| 출처 메모 | uspto-grants-2005_10 |
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