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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787767Generated: October 29, 2026

N-bromobutanimide → 7-bromo-9-pentyl-3-phenyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one

https://huagongshe.com/reaction/1787767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant9-pentyl-3-phenyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-oneHCID 57600206—
SolventTetrahydrofuranHCID 8028—
Product7-bromo-9-pentyl-3-phenyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-oneHCID 2506197923.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 9-pentyl-3-phenyl-6,9-dihydro-5h-[1,2,4]triazolo[4,3-a]purin-5-one (30 mg, 0.093 mmol) in THF (30 mL) was added N-bromosuccinimide (19.9 mg, 0.112 mmol). The mixture was stirred at 70° C. for 3 hours. The reaction mixture was concentrated in vacuo and the crude residue was purified using preparative LCMS to yield the desired product (8.7 mg, 23.3% yield). LCMS calculated for C17H18BrN6O(M+H): 401.1; found 401.1, 403.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511050B2
Source datasetuspto-grants-2009_03
ORD IDord-43868b42f769417590b8eda8ca745004
Source noteuspto-grants-2009_03