돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469733생성일: 2026년 10월 23일

Dimethylformamide → (S)-1-(3-chloro-5-trifluoromethyl-pyridin-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/469733

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물3-Chloro-2-fluoro-5-(trifluoromethyl)pyridineHCID 1268075—
반응물tert-Butyl 5-oxo-L-prolinateHCID 10888648—
용매Ammonium ChlorideHCID 25517—
생성물(S)-1-(3-chloro-5-trifluoromethyl-pyridin-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid tert-butyl esterHCID 67455590—

반응 단계

To a stirred solution of (S)-5-oxo-pyrrolidine-2-carboxylic acid tert-butyl ester (740 mg, 4 mmol) in N,N-dimethylformamide (5 mL) sodium hydride (180 mg of 60% dispersion in mineral oil, 4.5 mmol) is added at room temperature. After 10 minutes, 3-chloro-2-fluoro-5-trifluoromethylpyridine (1 mL, 8 mmol) is added and the suspension stirred at room temperature. After 3 h the reaction mixture is treated with saturated ammonium chloride solution (150 mL), extracted with dichloromethane (2×100 mL). Combined extracts washed with brine (2×50 mL), water, dried over anhydrous Na2SO4 and solvent removed in vacuo. The crude is purified by chromatography over silica gel eluting with hexanes/ethyl acetate to give the title compound, ESI m/z 365 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629157B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-43678106045c449a87c7dd4fb7cc0ff9
출처 메모uspto-grants-2014_01