HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 8-Acetoxy-3-bromo-2-methylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 8-Acetoxy-2-methylimidazo[1,2-a]pyridine | HCID 18321926 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 8-Acetoxy-3-bromo-2-methylimidazo[1,2-a]pyridine | HCID 18321874 | 86.9% |
Reaction Steps
To a solution of 8-acetoxy-2-methylimidazo[1,2-a]pyridine (100 mg) in ethanol (1 ml) was added N-bromosuccinimide (103 mg) under ice-cooling, and the mixture was stirred for 30 minutes at the same temperature. The mixture was diluted with ethyl acetate and washed with saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin layer chromatography (ethyl acetate) to give 8-acetoxy-3-bromo-2-methylimidazo[1,2-a]pyridine (123 mg) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06344462B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-6c44e0d5f89245489229f382bc9e3118 |
| Source note | uspto-grants-2002_02 |