HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxybromide → 2-Bromobenzo[4,5]imidazo[1,2-a]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | HCID 178516346 | HCID 178516346 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromobenzo[4,5]imidazo[1,2-a]pyrimidine | HCID 58362356 | 100% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Phosphorus oxybromide (25 g, 87 mmol) was added to a suspension of benzo[4,5]imidazo[1,2-a]pyrimidin-2-ol (5.2 g, 28.1 mmol) in DCE (Ratio: 1.000, Volume: 93 ml) and DMF (Ratio: 0.01, Volume: 0.927 ml). Heated the reaction mixture to 100° C. for 3 hours. Cooled the reaction to room temperature and concentrated. Diluted with ice water and quenched to pH ˜8 with concentrated ammonium hydroxide. The resulting residue was filtered and washed with water followed by ethyl ether. Dried under vacuum to afford crude 2-bromobenzo[4,5]imidazo[1,2-a]pyrimidine (6.97 g, 28.1 mmol, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691187B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-14df6210e34a49649043685d60def443 |
| Source note | uspto-grants-2014_04 |