HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Ethynyl-2-methylpyridine → HCID 45381859, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Ethynyl-2-methylpyridine | HCID 638197 | — |
| Reactant | HCID 67545385 | HCID 67545385 | — |
| Product | HCID 45381859 | HCID 45381859 | — |
Reaction Steps
The coupling of 9-(trifluoromethoxy)-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole (140 mg, 0.473 mmol; Example 175) and 5-ethynyl-2-methylpyridine (111 mg, 0.945 mmol; prepared as described in International Publication No. WO2005090333) was performed according to the procedure described in Example 20 to afford the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 1.66-1.80 (m, 2H), 1.84-1.98 (m, 2H), 2.40 (s, 3H), 2.95-3.23 (m, 5H), 4.24 (s, 2H), 6.83 (d, J=8 Hz, 1H), 6.92-6.99 (m, 2H), 7.06-7.16 (m, 3H), 7.28 (s, 1H), 7.85 (s, 1H); MS (DCI/NH3) m/z 414 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09063126B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-2f91df7f28994dfabb4027f992ec7a44 |
| Source note | uspto-grants-2015_06 |