HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → Ethyl imidazo[1,2-a]pyridine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl imidazo[1,2-a]pyridine-2-carboxylate | HCID 818807 | 60.3% |
Reaction Steps
A solution of 2-aminopyridine (5.0 g, 53.2 mmol) in THF (150 mL) was treated with ethyl bromopyruvate (10.32 g, 57.0 mmol) at room temperature followed by heating the mixture at reflux for 16 h. The resulting white precipitate was collected by Filtration and washed with THF (10 mL). Recrystallization of the solids from boiling EtOH (20 mL) gave ethyl imidazo[1,2-a]pyridine-2-carboxylate (6.10 g, 60% yield). ESI MS: m/z 191 [M+1]+. See, e.g., J. Med. Chem., 2003, 46, 3914-29.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249162B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-87fb08b070ce4000aa0c90363e3cacba |
| Source note | uspto-grants-2016_02 |