HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(4-Fluorophenyl)pyrazolo[1,5-a]pyrimidine | HCID 69297261 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine | HCID 83747438 | 76.1% |
Reaction Steps
To a solution of 2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine (5.8 g, 0.027 mol) in chloroform (60 mL) is added, at 0° C., N-bromosuccinimide (4.8 g, 0.027 mol). The mixture is stirred at room temperature for 1 h 30. The reaction mixture is then poured into water and extracted with dichloromethane (3×100 mL). The organic layer is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure. The crude material is filtered through a short pad of silica. 6 g (75%) of 3-bromo-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine are obtained as a brown solid which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023844B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-283af891170a41819dfe6340dae04fa3 |
| Source note | uspto-grants-2015_05 |