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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 874957생성일: 2026년 10월 25일

4-Cyanobutanoic acid → 6-(4-(4-Cyanobutanoyl)-3-methylpiperazin-1-yl)nicotinonitrile

https://huagongshe.com/reaction/874957

반응식

참여 물질

역할이름HCID투입량
반응물4-Cyanobutanoic acidHCID 38239—
반응물6-(3-Methylpiperazin-1-yl)nicotinonitrileHCID 62479801—
생성물6-(4-(4-Cyanobutanoyl)-3-methylpiperazin-1-yl)nicotinonitrileHCID 6732546085%

반응 단계

This compound was synthesized from 6-(3-methylpiperazin-1-yl)nicotinonitrile and 4-cyanobutyric acid as described for example 37 step 3 (900 mg, yield 85%) and it was carried through without further purification. 1H NMR (300 MHz, CDCl3) δ 8.41-8.40 (dd, J=2.3 Hz, 0.5 Hz, 1H), 7.67-7.63 (dd, J=9.0 Hz, 2.2 Hz, 1H), 6.61-6.58 (d, J=9.0 Hz, 1H), 4.46-4.19 (m, 4H), 3.54-3.36 (m, 2H), 3.16-3.11 (m, 2H), 2.59-2.51 (m, 3H), 2.06-2.01 (m, 2H), 1.26 (m, 3H). MS (ESI) m/z: Calculated for C16H19N6O: 297.16. found: 298.0 (M+H)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08981084B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-837d4ce2a0724fd19f6ab1bcef5eed92
출처 메모uspto-grants-2015_03