HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromopyruvate → 2,8-Diethyl imidazo[1,2-a]pyridine-2,8-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | Ethyl 2-aminopyridine-3-carboxylate | HCID 12433260 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2,8-Diethyl imidazo[1,2-a]pyridine-2,8-dicarboxylate | HCID 18983852 | 26.7% |
Reaction Steps
A mixture of ethyl bromopyruvate (2.3 g, 10.2 m mol and ethyl 2-aminonicotinate (1.7 g, 10 m mol) in methyl ethyl ketone (17 ml) was refluxed for 5 hours. After completion of the reaction, the mixture was cooled to room temperature and distilled under reduced pressure to remove the solvent. The residue to which saturated sodium hydrogen carbonate aqueous solution (50 ml) was added was extracted with chloroform (100 ml×3). The extract was washed with water, dried over MgSO4 and concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (eluent: ethyl acetate) to give the object compound (0.7 g, yield 26.7%) as crystals. m.p. 97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05498774 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-117e9f0b65764745badc6d7273b6fe6c |
| Source note | uspto-grants-1996_03 |