HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 7-chloro-3-(3,5-dimethoxyphenyl)-1-methyl-1,6-naphthyridin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3,5-dimethoxyphenylacetate | HCID 592191 | — |
| Reactant | 6-Chloro-4-(methylamino)nicotinaldehyde | HCID 23434571 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-chloro-3-(3,5-dimethoxyphenyl)-1-methyl-1,6-naphthyridin-2(1H)-one | HCID 86713576 | 80.8% |
Reaction Conditions
| Temperature | 105 °C |
|---|
Reaction Steps
A mixture of 6-chloro-4-(methylamino)nicotinaldehyde (3.7 g, 21.7 mmol), methyl 2-(3,5-dimethoxyphenyl)acetate (4.5 g, 21.7 mmol) and potassium carbonate (9.0 g, 65.1 mmol) in N,N-dimethylformamide (30 mL) was heated at 105° C. for 5 h. LCMS showed the reaction was completed. The reaction was cooled to RT, quenched with water (200 mL), and filtered. The filtration cake was washed by petroleum ether (50 mL) and ethyl acetate (50 mL) to afford the title compound (5.8 g, 77%) as a yellow solid. MS (ES+) C18H19ClN2O3 requires: 346, 348. Found: 347, 349 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126951B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-aa4daaab84e0467a98b543073ec60f0d |
| Source note | uspto-grants-2015_09 |