HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Methyl 2-(4,6-dimethoxypyrimidin-2-yloxy)-6-methylnicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-4,6-dimethoxypyrimidine | HCID 5152323 | — |
| Reactant | HCID 178497913 | HCID 178497913 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-(4,6-dimethoxypyrimidin-2-yloxy)-6-methylnicotinate | HCID 20095253 | 8% |
Reaction Steps
5.0 g (0.03 mol) of methyl 2-hydroxy-6-methylnicotinate, 5.0 g (0.03 mol) of potassium carbonate, 5.7 g (0.03 mol) of 2-chloro-4,6-dimethoxypyrimidine and 50 ml of N,N-dimethylformamide were weighed, and were reacted at 100° C. for 4 hours. The reaction mixture was then poured into water, and was extracted with 100 ml of ethyl acetate. The organic layer was then washed with water and a saturated sodium chloride aqueous solution. After drying with anhydrous sodium sulfate, the solvent was distilled off, and the residue was purified by silica gel column chromatography to obtain 0.73 g of the aimed product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05385880 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-9798b391204444be9315ebb2b3fecfb5 |
| Source note | uspto-grants-1995_01 |