HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl bromide → 1-(2-benzyloxy-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-5-yl)-2-bromo-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 2-(Benzyloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine | HCID 86706492 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-benzyloxy-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-5-yl)-2-bromo-ethanone | HCID 86706496 | — |
Reaction Steps
A solution of 2-(benzyloxy)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine (0.02 g, 0.087 mmol) in a DCM (1 mL) was treated with bromoacetyl bromide (7.6 μL, 17.6 mg, 0.087 mmol) at 0° C. The solvents were evaporated in vacuo to yield 1-(2-benzyloxy-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-5-yl)-2-bromo-ethanone as a white solid, that was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029366B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-8177760a94774f5fa09f57182d8e0aaf |
| Source note | uspto-grants-2015_05 |