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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 563138생성일: 2026년 10월 25일

3,5-Bis(trifluoromethyl)hydrocinnamic acid → N-[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-3-(3,5-bis-trifluoromethyl-phenyl)-N-(4-pentyl-benzyl)-propionamide

https://huagongshe.com/reaction/563138

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Bis(trifluoromethyl)hydrocinnamic acidHCID 1268098—
반응물1-(4-benzyl-piperazin-1-yl)-(S)-2-(4-pentyl-benzylamino)-3-phenyl-propan-1-oneHCID 59808255—
생성물N-[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-3-(3,5-bis-trifluoromethyl-phenyl)-N-(4-pentyl-benzyl)-propionamideHCID 1622642982%

반응 단계

Acylation of 1-(4-benzyl-piperazin-1-yl)-(S)-2-(4-pentyl-benzylamino)-3-phenyl-propan-1-one (43.5 mg, 0.09 mmol) according to the procedure described for the preparation of Example 1 with 3,5-bis-trifluoromethyl-hydrocinnamic acid (28.33 mg, 0.099 mmol) gave 55.5 mg (82%) of N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-3-(3,5-bis-trifluoromethyl-phenyl)-N-(4-pentyl-benzyl)-propionamide. LC-MS: tR=1.05 min; [M+H]+=752.45.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067419B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-b1f71e6e67aa4067a5292a7441af3c33
출처 메모uspto-grants-2011_11