참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Cyanuric fluoride | HCID 12664 | — |
| 반응물 | (2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acid | HCID 7021178 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester | HCID 87517560 | — |
반응 단계
To a solution of (2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyric acid (838 mg, 3.0 mmol) in dichloromethane (10 mL) at −35° C. was added dry pyridine (255 μL, 3.15 mmol) and cyanuric fluoride (375 μL, 4.5 mmol) under an atmosphere of dry argon. The mixture was stirred for 1.5 hours while maintaining the temperature between −35 and −25° C. A small amount of ice was added to the reaction mixture and the mixture stirred vigorously for 15 minutes. The organic layer was decanted away from the aqueous solution and the aqueous layer extracted with dichloromethane (2×10 mL). The combined organic layers were washed with ice cold water (15 mL), dried over sodium sulfate, filtered and concentrated in vacuo to give (1-fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester which was used in the subsequent step without further purification.
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-0dfd7448cbba4e059c35e0105354547d |
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| 출처 메모 | uspto-grants-2009_11 |
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