HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Bromoquinoline → HCID 45381391, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Bromoquinoline | HCID 521259 | — |
| Reactant | HCID 67543761 | HCID 67543761 | — |
| Product | HCID 45381391 | HCID 45381391 | — |
Reaction Steps
The reaction of 9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (230 mg, 1.0 mmol; Example 161) 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 1.95-2.22 (m, 4H) 2.96-3.03 (m, 1H) 3.09-3.29 (m, 4H) 4.32 (s, 2H) 6.86 (td, J=9, 2 Hz, 1H) 7.07-7.17 (m, 2H) 7.58-7.67 (m, 2H) 7.97 (d, J=2 Hz, 1H) 8.18 (d, J=9 Hz, 1H) 8.50 (d, J=8 Hz, 1H) 8.95 (dd, J=4, 2 Hz, 1H); MS (DCI/NH3) m/z 358 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09063126B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-9a45701991a746ad8a4618af5d4bd2f8 |
| Source note | uspto-grants-2015_06 |