HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 1-Benzoyl-3-cyano-4-methyl-pyrrolo[1,2-a]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 3-Methylquinoline | HCID 11926 | — |
| Reactant | HCID 21892121 | HCID 21892121 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Benzoyl-3-cyano-4-methyl-pyrrolo[1,2-a]quinoline | HCID 10425501 | — |
Reaction Steps
3-Methyl-1-phenacyl-quinolinium bromide: The title compound was prepared from 2-bromo-1-phenyl-ethanone (481 mg, 2.405 mmol), 3-methyl-quinoline (296 mg, 2.08 mmol) and acetonitrile (5 mL), similar to Example 1a, and yielded 640 mg (89%) as an off white solid: 1H NMR (CDCl3) 0.38 (d, J=1.8 Hz, 1H), 8.74 (s, 1H), 8.31 (m, 1H), 8.28 (m, 1H), 8.17 (dd, J=1.5, 8.4 Hz, 1H), 8.01 (m, 1H), 7.94–7.87 (m, 2H), 7.71 (m, 1H), 7.57 (t, J=7.8 Hz, 2H), 7.49 (s, 2H), 2.81 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135480B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-75840e5472614453991df0df02d35f8d |
| Source note | uspto-grants-2006_11 |