참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Chlorine monoxide | HCID 24646 | — |
| 반응물 | 4-Bromo-2-chloroaniline | HCID 610169 | — |
| 반응물 | (2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acid | HCID 7021178 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | (2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramide | HCID 69009703 | 55.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07612212B2 |
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| 출처 데이터셋 | uspto-grants-2009_11 |
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| ORD ID | ord-0c55c916f03d40cbb741710fd867c04b |
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| 출처 메모 | uspto-grants-2009_11 |
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