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HRID 1433748作成日:2026年10月27日

Trifluoroacetic acid → (2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramide

https://huagongshe.com/reaction/1433748

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Chlorine monoxideHCID 24646—
反応物4-Bromo-2-chloroanilineHCID 610169—
反応物(2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acidHCID 7021178—
溶媒PyridineHCID 1049—
生成物(2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramideHCID 6900970355.9%

反応条件

温度-20 °C

反応手順

4-Bromo-2-chloro-aniline (325 mg, 1.58 mmol) and (S,S)-2-tert-butoxycarbonylamino-3-phenyl-butyric acid (440 mg, 1.58 mmol) in pyridine (5 mL) were cooled to −30° C. Phosporus oxychloride (0.158 mL, 1.7 mmol) was added and stirred at −20° C. for 2 hours. The mixture was poured into ice water and extracted with ethyl acetate (3×). The combined organic extracts were washed with water, brine, dried over sodium sulfate and concentrated in vacuo. The residue was dissolved in dichloromethane (5 mL) at 0° C. and trifluoroacetic acid (3 mol) added. Stirring was continued for 2 hours at 0° C. The mixture was evaporated and the residue dissolved in ether. The ether solution was basified with saturated aqueous sodium bicarbonate and extracted with ether. The organic extracts were washed with brine, dried over sodium sulfate and evaporated to give (2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramide (325 mg, 55%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612212B2
出典データセットuspto-grants-2009_11
ORD IDord-0c55c916f03d40cbb741710fd867c04b
出典メモuspto-grants-2009_11