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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270836생성일: 2026년 10월 26일

(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acid → 4-{4-[2-(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperazin-1-yl}-benzonitrile

https://huagongshe.com/reaction/270836

반응식

참여 물질

역할이름HCID투입량
반응물(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acidHCID 1876853—
반응물4-(Piperazin-1-yl)benzonitrileHCID 2733995—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
생성물4-{4-[2-(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperazin-1-yl}-benzonitrileHCID 21071138—

반응 단계

Title compound was prepared following the HATU mediated coupling protocol P, wherein 1-(4-Cyanophenyl)-piperazine and (4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acid were used as the coupling components, to give the product as a solid: 1H NMR (CDCl3, 400 MHz) 7.44 (d, 2H), 6.77 (d, 2H), 4.90 (s, 2H), 3.67 (m, 4H), 3.29 (m, 4H), 2.22 (s, 3H) ppm; MS (ES) M+Na expected=434.0, found 434.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449576B1
출처 데이터셋uspto-grants-2008_11
ORD IDord-37fad470d94f446dba3a1f8f9a9e84ae
출처 메모uspto-grants-2008_11