HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 3-Carboethoxy-8-(2-ethyl-6-methylbenzyloxy)-2-methylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Ethyl-6-methylbenzyl chloride | HCID 12148918 | — |
| Reactant | Ethyl 8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxylate | HCID 21717316 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Carboethoxy-8-(2-ethyl-6-methylbenzyloxy)-2-methylimidazo[1,2-a]pyridine | HCID 21717356 | 68% |
Reaction Steps
A stirred mixture of 3-carboethoxy-8-hydroxy-2-methylimidazo[1,2-a]pyridine (0.92 g, 4.2 mmol), (0.7 g, 4.2 mmol) 2-ethyl-6-methylbenzylchloride (0.7 g, 4.2 mmol), sodium carbonate (1.0 g, 9.4 mmol) and a catalytic amount of potassium iodide in acetonitrile (40 ml) was refluxed for 4 h. After filtration and evaporation of the solvent under reduced pressure the residue was purified by column chromatography on silica gel using methylene chloride:ethylacetate as eluent to give 1.0 g, (68%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265415B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-331a24fd443f4862a9a0f3a0d33ff252 |
| Source note | uspto-grants-2001_07 |