HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 7-bromo-1H,2H,3H-pyrazolo(1,5-a)imidazole hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2,3-Dihydro-1H-imidazo(1,2-b)pyrazole | HCID 242471 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 7-bromo-1H,2H,3H-pyrazolo(1,5-a)imidazole hydrobromide | HCID 135539581 | 72% |
Reaction Steps
A 100-mL round-bottom flask was charged with 2,3-dihydro-1H-imidazo[1,2-b]pyrazole (1.7 g, 15.6 mmol) and acetic acid (5 mL). A solution of bromine (7.39 g, 46.2 mmol) in acetic acid (47 mL) was then added slowly. The resulting solution stirred for 3 h at room temperature. The reaction mixture was filtered and the filtrate was concentrated under vacuum to afford 7-bromo-2,3-dihydro-1H-imidazo[1,2-b]pyrazole hydrobromide (3.0 g, 72%) as a yellow solid. MS (ESI, pos. ion) m/z 188, 190 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388161B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-45c7491b04704cf98039878dd07ed3f3 |
| Source note | uspto-grants-2016_07 |