HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3,6,8-Tribromoimidazo[1,2-a]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6,8-Dibromoimidazo[1,2-a]pyrazine | HCID 15025843 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,6,8-Tribromoimidazo[1,2-a]pyrazine | HCID 14207622 | — |
Reaction Steps
N-bromosuccinimide (1.81 g, 10.15 mmol) was added to a solution of 6,8-Dibromo-imidazo[1,2-a]pyrazine (2.0 g, 10.15 mmol) in dichloromethane (40 ml). The reaction was stirred at room temperature over night then diluted with dichloromethane (100 ml) and washed with saturated aqueous sodium hydrogen carbonate (2×50 ml) and brine (50 ml). The organic layer was dried (MgSO4), filtered and concentrated in vaccuo. The product, 3,6,8-Tribromo-imidazo[1,2-a]pyrazine was obtained as a pink solid (2.77 g), sufficiently pure to be used in subsequent reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362018B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-0fb4b0376bbf47478e875a3846773a01 |
| Source note | uspto-grants-2013_01 |