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HRID 595792作成日:2026年10月27日

Ethyl Acetate → (+/-)-(3-Fluoro-4-((2,2,2-trifluoro-1-phenylethyl)carbamoyl)phenyl)boronic acid

https://huagongshe.com/reaction/595792

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物alpha-(Trifluoromethyl)benzenemethanamineHCID 89166—
反応物4-Carboxy-3-fluorophenylboronic acidHCID 2763201—
反応物N,N,3-trimethylbut-2-en-2-amineHCID 15569623—
溶媒DichloromethaneHCID 6344—
生成物(+/-)-(3-Fluoro-4-((2,2,2-trifluoro-1-phenylethyl)carbamoyl)phenyl)boronic acidHCID 123606597—

反応条件

温度0 °C

反応手順

A mixture of 4-borono-2-fluorobenzoic acid (54 mg, 0.294 mmol) in DCM (1468 μL) was cooled to 0° C. Then ghosez reagent N,N,3-trimethylbut-2-en-2-amine (65.8 μL, 0.587 mmol) was added and the whole mixture was stirred at rt for 20 min. The mixture was added into a mixture of TEA (246 μL, 1.762 mmol), 2,2,2-trifluoro-1-phenylethanamine (59.1 mg, 0.338 mmol) and DCM (1468 μL). The reaction was stirred at room temperature for 2 h. To the reaction mixture was added EtOAc, and washed with sat. sodium bicarbonate, water, and dried over Na2SO4. Filtered and concentrated to provide the crude product which was taken to the next step without further purification. LCMS (m/z): 342.2 (MH+), 0.84 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242996B2
出典データセットuspto-grants-2016_01
ORD IDord-49a1d99c282d4e52924273ca614f866f
出典メモuspto-grants-2016_01