Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408474Generated: October 30, 2026

N-bromobutanimide → 7-bromo-6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/2408474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidineHCID 67470335—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product7-bromo-6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidineHCID 6747029460%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815858B2
Source datasetuspto-grants-2014_08
ORD IDord-29caa8f3ac254f088cbeb43a78df9de0
Source noteuspto-grants-2014_08