HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (R)-methyl-3-(5-methoxypyridin-2-ylamino)-2-(oxirane-2-ylmethoxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (R)-(-)-Glycidyl-4-nitrobenzenesulfonate | HCID 14292098 | — |
| Reactant | Methyl-2-hydroxy-3-(5-methoxypyridin-2-ylamino)benzoate | HCID 67410207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-methyl-3-(5-methoxypyridin-2-ylamino)-2-(oxirane-2-ylmethoxy)benzoate | HCID 86761414 | 87.1% |
Reaction Steps
To a solution of methyl-2-hydroxy-3-(5-methoxypyridin-2-ylamino)benzoate 0.91 g (3.3 mmol) of step 4 in dimethylformamide 10 mL were (R)-glycidyl nosylate 1.0 g (4 mmol) and K2CO3 0.5 g (3.6 mmol), followed by stirring at room temperature for 12 hrs. The reaction mixture was concentrated in a vacuum, diluted with ethylacetate, and washed with distilled water and a saturated NaCl solution. After drying over magnesium sulfate and vacuum concentration, purification by column chromatography (developing solvent: ethylacetate/hexane=1/2) afforded 0.95 g of the title compound (yield 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026235B1 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-49aa13cd709f41898320ef564f6129ec |
| Source note | uspto-grants-2011_09 |