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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516837Generated: November 4, 2026

Water → 2-amino-3,5-dihydro-5-benzyl-4H-Pyrrolo[3,2-d]pyrimidin-4-one

https://huagongshe.com/reaction/1516837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
Reactant9-DeazaguanineHCID 135461003—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product2-amino-3,5-dihydro-5-benzyl-4H-Pyrrolo[3,2-d]pyrimidin-4-oneHCID 13598748588%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2-amino-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one (336.7 mg, 2.0 mmol) in CH2Cl2 (14.3 mL) was added benzyl bromide (0.26 mL, 2.2 mmol) and TBABr (644 mg, 2.0 mmol). The reaction mixture was cooled to 0° C., and to it was added 50% NaOH (1.7 mL). The resulting mixture was stirred for 2 h as it warmed from 0° C. to room temperature. Water was then added, and the solution was washed with CHCl3. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Purification by column chromatography, eluting with CH2Cl2/Acetone (5:1-1:1), afforded the product as a tan solid (423 mg, 82%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227601B2
Source datasetuspto-grants-2012_07
ORD IDord-ee04945824714ecba59c71c79af0fb6d
Source noteuspto-grants-2012_07