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HRID 469743作成日:2026年10月24日

Cesium carbonate → (S)-5-Oxo-1-(6-trifluoromethyl-pyridin-3-yl)-pyrrolidine-2-carboxylic acid tert-butyl ester

https://huagongshe.com/ja/reaction/469743

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Ethyl 2-oxocyclohexanecarboxylateHCID 95543—
反応物5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
反応物tert-Butyl 5-oxo-L-prolinateHCID 10888648—
触媒Copper bromide (CuBr2)HCID 24611—
溶媒Dimethyl SulfoxideHCID 679—
生成物(S)-5-Oxo-1-(6-trifluoromethyl-pyridin-3-yl)-pyrrolidine-2-carboxylic acid tert-butyl esterHCID 67456598—

反応条件

温度60 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629157B2
出典データセットuspto-grants-2014_01
ORD IDord-1ad5e847892741e98901bd738e33beba
出典メモuspto-grants-2014_01