HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl (ethoxymethylene)malonate → Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | 2,6-Dimethyl-3-pyridylamine | HCID 76964 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylate | HCID 22397159 | 30% |
Reaction Steps
A mixture of 2,6-dimethyl-3-aminopyridine (0.85 g) and diethyl ethoxymethylenemalonate (1.53 g) is heated at 135° C. in xylene (30 mL) for 2 h allowing for removal of ethanol. After the solvent is removed, the mixture is suspended in diphenyl ether (15 mL). The mixture is then heated to reflux with removal of ethanol for 30 min. The reaction mixture is cooled to room temperature and hexanes (20 mL) is added. The resulting precipitate is filtered, washed with diethyl ether (2×10 mL) and dried to give 0.5 g (30%) of the title compound as a brown solid. Physical chracteristics: MS (ESI+) m/z 247 (M+H)+; 1H NMR (DMSO) δ8.67, 7.97, 4.38, 2.85, 2.67, 1.40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06903097B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-5a6afead07e946eebdff6669cdb69237 |
| Source note | uspto-grants-2005_06 |