Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
7-Bromoquinoline → HCID 45381278, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 7-Bromoquinoline | HCID 521259 | — |
| 반응물 | HCID 67545626 | HCID 67545626 | — |
| 생성물 | HCID 45381278 | HCID 45381278 | — |
반응 단계
The reaction of 3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (212 mg, 1.0 mmol; Example 187A) and 7-bromoquinoline (312 mg, 1.5 mmol; Ark Pharm) was performed as described in Example 68 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.96-2.23 (m, 4H) 2.99-3.05 (m, 1H) 3.10-3.30 (m, 4H) 4.37 (s, 2H) 7.07-7.21 (m, 3H) 7.40-7.49 (m, 1H) 7.59-7.69 (m, 2H) 7.97 (d, J=2 Hz, 1H) 8.17 (d, J=9 Hz, 1H) 8.50 (d, J=7 Hz, 1H) 8.95 (dd, J=4, 2 Hz, 1H); MS (DCI/NH3) m/z 340 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09063126B2 |
| 출처 데이터셋 | uspto-grants-2015_06 |
| ORD ID | ord-6c6b55a067394ac1838e0be9252faeba |
| 출처 메모 | uspto-grants-2015_06 |