HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → 2-(2-Bromophenyl)imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 2-Bromophenacyl Bromide | HCID 2737522 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Bromophenyl)imidazo[1,2-a]pyridine | HCID 2862388 | — |
Reaction Steps
A solution of 2-aminopyridine (1.63 g) and 2-bromo-1-(2-bromophenyl)-ethanone (4.8 g) in dry ethanol (40 mls) was heated under reflux for 1 hour. The mixture was concentrated in vacuo. The residue was treated with dilute sodium bicarbonate solution and extracted with ethyl acetate. The ethyl acetate was washed with water and brine then dried and evaporated. Flash chromatography produced the sub-title compound as a light grey oil. MS MW 272/274 bp 272.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04900751 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-5dac21755698435cbc12774be3fba360 |
| Source note | uspto-grants-1990_02 |