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HRID 469733作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物3-Chloro-2-fluoro-5-(trifluoromethyl)pyridineHCID 1268075—
反応物tert-Butyl 5-oxo-L-prolinateHCID 10888648—
溶媒Ammonium ChlorideHCID 25517—
生成物(S)-1-(3-chloro-5-trifluoromethyl-pyridin-2-yl)-5-oxo-pyrrolidine-2-carboxylic acid tert-butyl esterHCID 67455590—

反応手順

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]+.

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-43678106045c449a87c7dd4fb7cc0ff9
出典メモuspto-grants-2014_01