HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-butoxy-N-quinolin-3-yl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminoquinoline | HCID 11375 | — |
| Reactant | 4-Butoxybenzoyl chloride | HCID 118561 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-butoxy-N-quinolin-3-yl-benzamide | HCID 10471252 | 84% |
Reaction Steps
4-Butoxy-benzoyl chloride (0.21 mL, 1.11 mmol), Et3N (0.16 mL, 1.15 mL) and 3-aminoquinoline (0.153 g, 1.06 mmol) were stirred together in 10 mL acetonitrile in a round bottom flask for 4 hours. The reaction mixture was then evaporated in vacuo and the residue was triturated with 5 mL acetonitrile. The resulting solid was collected by filtration, rinsed with acetonitrile and dried to yield the title product as a cream-colored powder (0.284 g, 0.89 mmol). 1H NMR (CDCl3): δ 8.91 (s, 2H), 8.20 (s, 1H), 8.08 (d, 1H), 7.94 (d, 2H), 7.84 (d, 1H), 7.67 (t, 1H), 7.57 (t, 1H), 7.01 (d, 2H), 4.05 (t, 2H), 1.83 (p, 2H), 1.52 (h, 2H), 1.01 (t, 3H); MS: m/z 321.0 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394828B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-d937c47bcad34df1b7d255e8c71a6229 |
| Source note | uspto-grants-2013_03 |