関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexamethylphosphoramide | HCID 12679 | — |
| 反応物 | 3-(Trimethylstannyl)pyridine | HCID 10868445 | — |
| 反応物 | Ethyl 7-bromo-1-ethyl-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 14851995 | — |
| 反応物 | Chloroform ethanol | HCID 21889567 | — |
| 触媒 | HCID 178418476 | HCID 178418476 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | Ethyl 1,4-dihydro-1-ethyl-7-(3-pyridinyl)4-oxo-3-quinolinecarboxylate | HCID 21790907 | 56.3% |
反応手順
A suspension of 10.0 g ethyl 7-bromo-1,4-dihydro-1-ethyl-4-oxo-3-quinolinecarboxylate (U.S. Pat. No. 3,753,993), 0.64 g dichlorobis(triphenylphosphine)palladium, 10.9 g 3-trimethylstannylpyridine and 6.5 ml hexamethylphosphoramide in 40 ml dioxane was heated at reflux under nitrogen for 48 hrs. The reaction mixture was filtered through neutral alumina, eluted with chloroform, washed with water, and dried over potassium carbonate. The solid product obtained by concentration in vacuo was subjected to chromatography (MPLC; 10:1 CHCl3/EtOH) to give 5.6 g of ethyl 1,4-dihydro-1-ethyl-7-(3-pyridinyl)4-oxo-3-quinolinecarboxylate, which was hydrolyzed by refluxing with 150 ml 3N hydrochloric acid for 1.5 hrs. The product which separated (3.9 g) was dried to give 1,4-dihydro-1-ethyl-7-(3-pyridinyl)-4-oxo-3-quinolinecarboxylic acid, m.p. 268-269° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04959363 |
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| 出典データセット | uspto-grants-1990_09 |
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| ORD ID | ord-79c42d546171496696d100287e0aafdc |
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| 出典メモ | uspto-grants-1990_09 |
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