HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyl Ether → Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Diethyl 2-((5-bromopyridin-3-ylamino)methylene)malonate | HCID 67318826 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate | HCID 13459134 | — |
Reaction Steps
In a RBF fitted with a reflux condenser a mixture of diethyl 2-((5-bromopyridin-3-ylamino)methylene)malonate (1 g, 3 mmol) and 1-phenoxybenzene (10 mL, 63 mmol) was heated to reflux for 1 h. The reaction mixture was allowed to cool to RT and CH3CN was added. The resulting solids were filtered and dried to provide the desired product as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981891B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-0aef46e3251f4e13a794bf0434f5c1f2 |
| Source note | uspto-grants-2011_07 |