関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Ethyl 2-oxocyclohexanecarboxylate | HCID 95543 | — |
| 反応物 | 5-Bromo-2-(trifluoromethyl)pyridine | HCID 2761197 | — |
| 反応物 | tert-Butyl 5-oxo-L-prolinate | HCID 10888648 | — |
| 触媒 | Copper bromide (CuBr2) | HCID 24611 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | (S)-5-Oxo-1-(6-trifluoromethyl-pyridin-3-yl)-pyrrolidine-2-carboxylic acid tert-butyl ester | HCID 67456598 | — |
反応手順
A solution of cesium carbonate (1.539 g; 4.725 mmol), copper bromide (0.032 g; 0.225 mmol) and ethyl-2-oxocyclohexanecarboxylate (0.072; 0.45 mmol) in anhydrous dimethyl sulfoxide (1.25 mL) is degassed with argon and stirred 30 minutes. To this solution is added (S)-5-oxo-pyrrolidine-2-carboxylic acid tert-butyl ester (0.5 g; 2.699 mmol) and 5-bromo-2-trifluoromethylpyridine (0.508 g; 2.25 mmol) in 1 mL anhydrous dimethyl sulfoxide. The mixture is heated in a sealed tube to 60° C. in an oil bath and stirred overnight. The reaction mixture is cooled to room temperature, filtered through Celite® and washed with ethyl acetate. The combined organics are washed with brine, dried over sodium sulfate and concentrated under reduced pressure. ESI m/z 331 [M+H]+
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08629157B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-1ad5e847892741e98901bd738e33beba |
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| 出典メモ | uspto-grants-2014_01 |
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