HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Bromoacetophenone → 2-(4-Bromophenyl)imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Bromophenyl)imidazo[1,2-a]pyridine | HCID 623416 | 85% |
Reaction Steps
Dissolving 15 g (54 mmol) of 4-bromoacetophenone and 5.2 g (55 mmol) of 2-aminopyridine into 100 milliliter of ethanol, adding 7.0 g of sodium hydroxide, the resultant suspension was refluxed under heating for 6 hours. After completion of the reaction, resultant crystals were separated with filtration, washed with water and ethanol, thereby obtaining 12.5 g of 2-(4-bromo-phenyl)-imidazo [1,2-a] pyridine (yield: 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07867629B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-51c6f98e38224fa1b37f06b79058030e |
| Source note | uspto-grants-2011_01 |