HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 6-Chloro-1-methyl-4-oxo-1,4-dihydro[1,5]naphthyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 6-chloro-4-hydroxy[1,5]naphthyridine-3-carboxylate | HCID 178469542 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 6-Chloro-1-methyl-4-oxo-1,4-dihydro[1,5]naphthyridine-3-carboxylate | HCID 22397136 | 65% |
Reaction Steps
A mixture of ethyl 6-chloro-4-hydroxy[1,5]naphthyridine-3-carboxylate (Preparation 58, 694 mg), potassium carbonate (588 mg), and iodomethane (264 μL) in DMF (15 mL) is stirred at room temperature for 5 hours. The mixture is poured into water (50 mL), and the solution is extracted with CH2Cl2 (3×50 mL). The organic layers are dried (MgSO4) and concentrated. Trituration with ether (50 mL) affords 473 mg (65%) of the title compound as an off-white solid. Physical Characteristics. 1H NMR (DMSO-d6) δ8.70, 8.31, 7.90, 4.24, 3.92, 1.29; HRMS (FAB) m/z 267.0535 (C12H11ClN2O3+H). Anal. Found: C, 54.14; H, 4.24; N, 10.58.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06903097B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-2f89db75b04f478a8ef350bb3765390a |
| Source note | uspto-grants-2005_06 |