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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787787Generated: October 30, 2026

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

https://huagongshe.com/reaction/1787787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-(3-bromobenzyl)-9-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-oneHCID 57600160—
SolventTetrahydrofuranHCID 8028—
Product7-bromo-9-pentyl-3-(3-bromobenzyl)-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-oneHCID 2506279160.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

To the solution of 3-(3-bromobenzyl)-9-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one (210 mg, 0.50 mmol) in tetrahydrofuran (20 mL) was added N-bromosuccinimide (140 mg, 0.00076 mol). The mixture was stirred at 70° C. for 1 hour. The reaction mixture was concentrated and the residue was purified by preparative LCMS to yield the desired product (0.15 g, 60%). 1HNMR (300 MHz, d6-DMSO): δ 7.16 (d, J=8.3 Hz, 2H), 6.81 (d, J=8.3 Hz, 2H), 4.46 (s, 3H), 4.20 (t, J=7.2 Hz, 2H), 3.67 (s, 2H), 1.79 (m, 2H), 1.28 (m, 4H), 0.83 (m, 3H). LCMS calculated for C18H19Br2N6O(M+H): 493; found: 493, 495 and 497.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511050B2
Source datasetuspto-grants-2009_03
ORD IDord-fa37744ffd204ae0bda5eb08decedb0f
Source noteuspto-grants-2009_03