HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → HCID 178516370, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 178524700 | HCID 178524700 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178516370 | HCID 178516370 | 88.9% |
Reaction Steps
In a RBF fitted with a reflux condenser, 7-bromo-4-hydroxy-1,5-naphthyridine-3-carboxylic acid (1 g, 4 mmol) was added in portions over 10 minutes to stirred refluxing quinoline (50 mL), and the resulting mixture was refluxed for 1 h. The mixture was cooled and diluted with acetone. The precipitate was filtered, washed with water and dried to give 0.8 g of a grey-brown powder. The product was reprecipitated from aq. NaOH with glacial acetic acid to give a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776857B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-ae83a504a2634e90974b367c7895202f |
| Source note | uspto-grants-2010_08 |