Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Cyanobutanoic acid → 6-(4-(4-Cyanobutanoyl)-3-methylpiperazin-1-yl)nicotinonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Cyanobutanoic acid | HCID 38239 | — |
| 반응물 | 6-(3-Methylpiperazin-1-yl)nicotinonitrile | HCID 62479801 | — |
| 생성물 | 6-(4-(4-Cyanobutanoyl)-3-methylpiperazin-1-yl)nicotinonitrile | HCID 67325460 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08981084B2 |
| 출처 데이터셋 | uspto-grants-2015_03 |
| ORD ID | ord-837d4ce2a0724fd19f6ab1bcef5eed92 |
| 출처 메모 | uspto-grants-2015_03 |