HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-4'-methylacetophenone → Methyl 2-(4-methylphenyl)imidazo[1,2-a]pyridine-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-4'-methylacetophenone | HCID 69272 | — |
| Reactant | Methyl 6-aminonicotinate | HCID 737487 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 2-(4-methylphenyl)imidazo[1,2-a]pyridine-6-carboxylate | HCID 16088231 | 85.4% |
Reaction Steps
2-Bromo-4′-methylacetophenone 2 (14.5 g, 65.1 mmol) was added to a hot solution of methyl 2-aminopyridine-5-carboxylate 1 (9.0 g, 61.1 mmol) in ethanol (280 ml). The solution was then heated at reflux for 6 h, cooled to room temperature and the white solid filtered and washed with ethanol to give methyl 2-(4-tolyl)-imidazo[1,2-a]pyridine-6-carboxylate 3 (13.9 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673652B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-07e84fe958d141a1bd7ef71b27958dfa |
| Source note | uspto-grants-2014_03 |