Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 563133생성일: 2026년 10월 24일
Water → N-[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(4-trifluoromethyl-phenyl)-acrylamide
https://huagongshe.com/ko/reaction/563133
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 4-(Trifluoromethyl)cinnamic acid | HCID 688070 | — |
| 반응물 | 1-(4-benzyl-piperazin-1-yl)-(S)-2-(4-pentyl-benzylamino)-3-phenyl-propan-1-one | HCID 59808255 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Diisopropylethylamine | HCID 81531 | — |
| 생성물 | N-[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(4-trifluoromethyl-phenyl)-acrylamide | HCID 67005150 | 58.8% |
반응 단계
In an inert atmosphere, trans-4-trifluoromethyl-cinnamic acid (21.4 mg, 0.099 mmol) was dissolved in 2 mL dichloromethane followed by the addition of 1-chloro-N,N-2-trimethylpropenyl amine (16.4 μl, 0.122 mmol). Stirring was continued at rt for 1 h. This solution was then added to a solution of 1-(4-benzyl-piperazin-1-yl)-(S)-2-(4-pentyl-benzylamino)-3-phenyl-propan-1-one (43.5 mg, 0.09 mmol) in dichloromethane (1 mL) and Hünig's base (39 μl). The resulting mixture was stirred for 1 h at rt, followed by the addition of water (3 mL). The layers were separated. The aq. layer was extracted with dichloromethane (2×2 mL) and the combined organic layers were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by prep. TLC (silicagel, heptane/EtOAc=1/1) to give 36.1 mg (58%) of N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(4-trifluoromethyl-phenyl)-acrylamide. LC-MS: tR=1.02 min; [M+H]+=682.48.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08067419B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-98c6c7f654ca4cba9463d0ddf55e7b70 |
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| 출처 메모 | uspto-grants-2011_11 |
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