HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Bromoisoquinoline → HCID 45381506, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Bromoisoquinoline | HCID 12257441 | — |
| Reactant | HCID 67544841 | HCID 67544841 | — |
| Product | HCID 45381506 | HCID 45381506 | — |
Reaction Steps
The reaction of 9-methyl-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (226 mg, 1.0 mmol; Example 2B) and 7-bromoisoquinoline (312 mg, 1.5 mmol; Frontier) was performed as described in Example 68 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.94-2.20 (m, 4H) 2.42 (s, 3H) 2.91-2.98 (m, 1H) 3.08-3.29 (m, 4H) 4.32 (s, 2H) 6.90-6.96 (m, 1H) 6.98-7.04 (m, 1H) 7.22 (s, 1H) 7.73 (dd, J=8, 2 Hz, 1H) 7.94 (d, J=6 Hz, 1H) 8.09 (d, J=2 Hz, 1H) 8.15 (d, J=9 Hz, 1H) 8.53 (d, J=6 Hz, 1H) 9.33 (s, 1H); MS (DCI/NH3) m/z 354 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09063126B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-9dc1bff11be34a43af1bd481faa1011d |
| Source note | uspto-grants-2015_06 |