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HRID 55988作成日:2026年10月26日

Water → N-[2-(3,5-dichloropyridin-2-yl)-2-(propoxyimino)ethyl]-2-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/55988

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
反応物2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-O-propyloximeHCID 118071509—
溶媒DichloromethaneHCID 6344—
生成物N-[2-(3,5-dichloropyridin-2-yl)-2-(propoxyimino)ethyl]-2-(trifluoromethyl)benzamideHCID 11807157287.2%

反応手順

In a solution of 151 mg of 2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-O-propyloxime and 86 mg of triethylamine in 4 ml of dichloromethane, 154 mg of 2-(trifluoromethyl)benzoyl chloride was added dropwise with stirring under cooling with ice, and after the addition, the mixture was stirred at room temperature for another 2 hours. After completion of the reaction, the reaction mixture was mixed with 10 ml of water and extracted with chloroform (30 ml×1), the resulting organic layer was washed with water (10 ml×1) and dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 2:8 to 3:7) as the eluent to obtain 218 mg of the desired product as a pale yellow resinous substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434684B2
出典データセットuspto-grants-2016_09
ORD IDord-c97955ef590e42a7aa823e60611fccb8
出典メモuspto-grants-2016_09