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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1433748생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1433748

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Chlorine monoxideHCID 24646—
반응물4-Bromo-2-chloroanilineHCID 610169—
반응물(2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acidHCID 7021178—
용매PyridineHCID 1049—
생성물(2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramideHCID 6900970355.9%

반응 조건

온도-20 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612212B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-0c55c916f03d40cbb741710fd867c04b
출처 메모uspto-grants-2009_11