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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 875014생성일: 2026년 10월 25일

3-Fluoro-4-piperazin-1-yl-benzonitrile → 3-Fluoro-4-(4-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoyl)piperazin-1-yl)benzonitrile

https://huagongshe.com/reaction/875014

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluoro-4-piperazin-1-yl-benzonitrileHCID 596113—
반응물3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acidHCID 25180854—
생성물3-Fluoro-4-(4-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoyl)piperazin-1-yl)benzonitrileHCID 5332792438%

반응 단계

This compound was synthesized from 3-fluoro-4-(piperazin-1-yl)benzonitrile and 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described for example 37 step 3 (100 mg, yield 38%). 1H NMR (400 MHz, DMSO-d6) δ 8.17-8.15 (dt, J=6.6 Hz, 1.7 Hz, 1H), 8.09 (s, 1H), 7.75-7.72 (m, 3H), 7.61-7.58 (dd, J=8.5 Hz, 1.5 Hz, 1H), 7.17-7.13 (t, J=8.7 Hz, 1H), 3.81 (m, 2H), 3.52 (m, 2H), 3.19 (m, 4H). MS (ESI) m/z: Calculated for C21H15F4N5O2: 445.12. found: 446.2 (M+H)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08981084B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-171168492c674416adfe78fffc1f8c11
출처 메모uspto-grants-2015_03