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 | Ethanol | HCID 702 | — |
| Product | Ethyl imidazo[1,2-a]pyridine-2-carboxylate | HCID 818807 | 62.8% |
Reaction Steps
A solution of 2-amino-pyridine (2 g, 21 mmol) and ethyl bromopyruvate (4.14 g, 21 mmol) in ethanol (31 mL) was stirred under reflux for 24 h. The solvent was evaporated, and the residue was dissolved in a minimum volume of water. The solution was neutralized (pH==8) with saturated NaHCO3. The aqueous layer was extracted with AcOEt and the organic layer was washed with saturated NaCl. The solvent was removed under pressure to afford 2.51 g of ethyl imidazo[1,2-a]pyridine-2-carboxylate (Yield: 62%) as an orange oil which can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101637B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-c361042467c649bc951765f1e2d39888 |
| Source note | uspto-grants-2012_01 |