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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469743생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Ethyl 2-oxocyclohexanecarboxylateHCID 95543—
반응물5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
반응물tert-Butyl 5-oxo-L-prolinateHCID 10888648—
촉매Copper bromide (CuBr2)HCID 24611—
용매Dimethyl SulfoxideHCID 679—
생성물(S)-5-Oxo-1-(6-trifluoromethyl-pyridin-3-yl)-pyrrolidine-2-carboxylic acid tert-butyl esterHCID 67456598—

반응 조건

온도60 °C

반응 단계

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]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629157B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-1ad5e847892741e98901bd738e33beba
출처 메모uspto-grants-2014_01