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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 563134생성일: 2026년 10월 25일

m-(Trifluoromethyl)cinnamic acid → N-[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(3-trifluoromethyl-phenyl)-acrylamide

https://huagongshe.com/reaction/563134

반응식

참여 물질

역할이름HCID투입량
반응물m-(Trifluoromethyl)cinnamic acidHCID 719451—
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]-N-(4-pentyl-benzyl)-3-(3-trifluoromethyl-phenyl)-acrylamideHCID 6700529969.9%

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 trans-3-trifluoromethyl-cinnamic acid (21.4 mg, 0.099 mmol) gave 42.9 mg (69%) of N—[(S)-1-benzyl-2-(4-benzyl-piperazin-1-yl)-2-oxo-ethyl]-N-(4-pentyl-benzyl)-3-(3-trifluoromethyl-phenyl)-acrylamide. LC-MS: tR=1.02 min; [M+H]+=682.48.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067419B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-54732595803e48a389fc5d5c3246b3fc
출처 메모uspto-grants-2011_11