HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyridinamine, 5-iodo- → 2-Ethyl-6-iodo-3-methylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyridinamine, 5-iodo- | HCID 88579 | — |
| Reactant | 2-Bromo-3-pentanone | HCID 545092 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Ethyl-6-iodo-3-methylimidazo[1,2-a]pyridine | HCID 23158252 | 30.8% |
Reaction Steps
To a stirred mixture of 2-bromopentan-3-one (2.0 g), 2-amino-5-iodopyridine (1.0 g) and EtOH (50 ml) was heated at reflux for 16 h. The reaction mixture was cooled and concentrated in vacuo. The residue was diluted with water (100 ml), and extracted with DCM. The DCM layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/EtOAc) to give the title compound (400 mg) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365540B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-b3768ba3442b4f679e7065f6d0567b05 |
| Source note | uspto-grants-2016_06 |