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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244452Generated: October 30, 2026

N-bromobutanimide → 7-Bromo-1,5-dihydro-4H-pyrrolo[3,2-D]pyrimidin-4-one

https://huagongshe.com/reaction/244452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant9-DeazahypoxanthineHCID 135488881—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-Bromo-1,5-dihydro-4H-pyrrolo[3,2-D]pyrimidin-4-oneHCID 135743711—

Reaction Steps

A mixture of 3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one (200 mg, 1.5 mmol, 1 equiv.) and N-bromosuccinimide (320 mg, 1.8 mmol, 1.2 equiv.) in 10 mL of DMF was stirred for 18 hours at room temperature. The reaction was diluted with water and resulting solid was collected by filtration, dried, suspended in MeOH, and filtered. The filtrate was concentrated in vacuo to provide 7-bromo-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one as a beige solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658637B2
Source datasetuspto-grants-2014_02
ORD IDord-a550ae5e2aa142108b291cbe43087a57
Source noteuspto-grants-2014_02