HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-methylpyridine → 2-(4-Bromophenyl)-7-methylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-methylpyridine | HCID 1533 | — |
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Bromophenyl)-7-methylimidazo[1,2-a]pyridine | HCID 717644 | 56.8% |
Reaction Steps
A mixture of 2,4′-dibromoacetophenone (22.4 g) and 2-amino-4-picoline (8.68 g) in ethanol (80 mL) was heated at reflux temperature for 3 hours. The reaction mixture was cooled to ambient temperature and the crystalline solid isolated by filtration, washed with ethanol and dried in vacuo to give the title compound (13.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041828B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-92c5406e58da42a0beedbb38852dd4ef |
| Source note | uspto-grants-2006_05 |