HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-bromo-6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidine | HCID 67470335 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-bromo-6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidine | HCID 67470294 | 60% |
Reaction Steps
To a slurry of 6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidine (1.0 g) in acetone (50 mL) was added N-bromosuccinimide (1.0 g). The reaction was stirred at rt for 2 h, until complete conversion was observed by LC-MS. The reaction mixture was diluted with EtOAc (150 mL) and the solid was collected via filtration and washed with EtOAc yielding 820 mg of desired (60% yield). LCMS calculated for C12H7BrFN3 292.1, found 292.23: [M+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815858B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-29caa8f3ac254f088cbeb43a78df9de0 |
| Source note | uspto-grants-2014_08 |