HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 67530603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(2,4-dimethoxybenzylamino)acetate | HCID 19895532 | — |
| Reactant | HCID 67530800 | HCID 67530800 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67530603 | HCID 67530603 | 51.5% |
Reaction Steps
4-Bromomethyl-3-ethyl-isoxazole-5-carboxylic acid ethyl ester (1.03 g, 3.93 mmol) was dissolved in 40 mL of acetonitrile. N-(2,4-dimethoxybenzyl)glycine ethyl ester (1.09 g, 4.32 mmol), potassium carbonate (1.63 g, 11.8 mmol) and potassium iodide (0.98 g, 5.90 mmol) were added, and the mixture was stirred at room temperature for 16 h. The solvent was removed in vacuo and the residue was partitioned between CH2Cl2 and water. The aqueous layer was extracted with additional CH2Cl2 and the combined organic layer was dried over MgSO4 and concentrated. The crude oil was purified by flash chromatography (0-30% EtOAc/hexanes) to give 0.88 g of the title compound. MS: (+) m/z 435.53 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08269008B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-13de6047a7464157939151fb7596b032 |
| Source note | uspto-grants-2012_09 |