HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2-[3-(2-Methyl-2-nitropropyl)imidazo[1,2-a]pyridin-7-yloxy]-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetamide | HCID 6580 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178441236 | HCID 178441236 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2-[3-(2-Methyl-2-nitropropyl)imidazo[1,2-a]pyridin-7-yloxy]-acetamide | HCID 22038569 | 34.3% |
Reaction Steps
3-(2-Methyl-2-nitropropyl)imidazo[1,2-a]pyridin-7-ol (1.5 g, 6.38 mmol), chloroacetamide (1.19 g, 12.73 mmol), potassium carbonate (6.4 mmol) and a small amount of potassium iodide in 2-butanone (30 ml) is heated at reflux overnight. The solids are removed by filtration and the filtrate is concentrated under reduced pressure. The residue is chromatographed on silica gel with dichloromethane/methanol 3:1 to 1:1 to give 640 mg of 2-[3-(2-methyl-2-nitropropyl)imidazo[1,2-a]pyridin-7-yloxy]-acetamide (34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205407B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-1d287d2700084bc5896f302435ac8b9f |
| Source note | uspto-grants-2007_04 |