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HRID 507991作成日:2026年10月27日
Dimethylformamide → methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate
https://huagongshe.com/reaction/507991
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-Methyl-1,2,3,4-tetrahydroquinoline | HCID 96289 | — |
| 反応物 | Methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate | HCID 23157330 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate | HCID 23157488 | 75% |
反応手順
A mixture of methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate (0.70 g, 2.2 mmol), 2-methyl-1,2,3,4-tetrahydroquinoline (0.39 g, 2.6 mmol), potassium carbonate (0.60 g, 4.3 mmol) and N,N-dimethylformamide (14 mL) was stirred at 70° C. for 23 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-2/1) to give the title compound (0.63 g, yield 75%) as a pale-yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07786165B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-6312856ef23848778fe07efbc22e69ae |
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| 出典メモ | uspto-grants-2010_08 |
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