HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Methylquinoline → HCID 21892120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Methylquinoline | HCID 11927 | — |
| Reactant | 2-Bromo-1-(4-fluorophenyl)ethan-1-one | HCID 96749 | — |
| Reactant | HCID 21892141 | HCID 21892141 | — |
| Product | HCID 21892120 | HCID 21892120 | — |
Reaction Steps
1-[2-(4-Fluoro-phenyl)-2-oxo-ethyl]-7-methyl-quinolinium bromide: The title compound was prepared from 2-bromo-(4-fluoro-phenyl) ethanone (0.352 g, 2.46 mmol) and 7-methyl-quinoline (0.71 g, 3.27 mmol), by a method similar to that described for the preparation of Example 1a, and yielded 0.741 g (84%). 1H NMR (DMSO-d6): 9.42 (dd, J=16.2, 5.7 Hz, 2H), 8.44 (d, J=8.4 Hz, 1H), 8.35 (s, 1H), 8.24 (m, 3H), 7.92 (d, J=8.4 Hz, 1H), 7.56 (m, 2H), 6.95 (s, 2H), 2.60 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135480B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-d5e91233905241709d58e8039a92c8a2 |
| Source note | uspto-grants-2006_11 |