Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Hydroxyquinoline → HCID 25142638, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Hydroxyquinoline | HCID 6038 | — |
| 반응물 | 1-(3-Aminopropyl)-4-(2-methoxyphenyl)piperazine | HCID 10467259 | — |
| 반응물 | 2-Oxo-1,2,3,4-tetrahydroquinoline-7-carboxylic acid | HCID 13243001 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | HCID 25142638 | HCID 25142638 | — |
반응 단계
N-(3-(4-(2-methoxyphenyl)piperazin-1-yl)propyl)-2-oxo-1,2,3,4-tetrahydroquinoline-7-carboxamide (35) (Scheme 6) was prepared from 3-(4-(2-methoxyphenyl)piperazin-1-yl)propan-1-amine (34) and 2-oxo-1,2,3,4-tetrahydroquinoline-7-carboxylic acid (22) according to the protocol described for the compound 23 (Scheme 4, Example 35). Colorless oil (0.1 g, 20%). 1H NMR (400 MHz, CDCl3): δ 1.67 (quintet, J=6.4 Hz, 2H); 1.73-1.78 (m, 2H); 2.62 (t, J=8.0 Hz, 2H); 2.70 (broad s, 4H); 3.05-3.08 (m, 5H); 3.47-3.49 (m, 2H); 3.85 (s, 3H); 4.21 (t, J=5.6 Hz, 2H); 6.86 (d, J=7.6 Hz, 1H); 6.92-6.95 (m, 2H); 6.98-7.03 (m, 1H); 7.35 (d, J=1.2 Hz, 1H); 7.52 (dd, J=6.0, 3.6 Hz, 1H); 7.70 (dd, J=6.0, 3.6 Hz, 1H). MS (ESI): m/z=404.5 (M+−H2O).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08247420B2 |
| 출처 데이터셋 | uspto-grants-2012_08 |
| ORD ID | ord-1ce2d898def140dc88b6b625f3d13c74 |
| 출처 메모 | uspto-grants-2012_08 |