関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 8-Hydroxyquinoline | HCID 1923 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 1-Chloro-4-iodobenzene | HCID 12510 | — |
| 反応物 | HCID 178425430 | HCID 178425430 | — |
| 触媒 | HCID 178419072 | HCID 178419072 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 1-(4-Chlorophenyl)-3-(2,5-dimethylpyrrol-1-yl)-1H-pyrazole | HCID 86680367 | 96.5% |
反応手順
Under argon atmosphere, to a solution of 3-(2,5-dimethylpyrrol-1-yl)-1H-pyrazole (3.06 g) prepared according to the same procedures as Preparation 4 in N-methylpyrrolidone (31 ml) were sequentially added cesium carbonate (12.37 g), 8-quinolinol (0.55 g), copper (I) oxide (0.27 g) and 1-chloro-4-iodobenzene (6.79 g) at room temperature, the mixture was stirred at 110° C. for 2 hours. This reaction mixture was cooled to room temperature, and then toluene (30 ml) was added thereto, the mixture was filtered through Celite, and further subjected to elution with toluene. The filtrate was sequentially washed with a 1N aqueous solution of sodium hydroxide, water, a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/0 to 9/1) to give the titled compound (4.98 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846746B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-7b4191a76f0643c9b6f8e47b5d240bc2 |
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| 出典メモ | uspto-grants-2014_09 |
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