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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291397Generated: October 25, 2026

Sodium hydride → 7-[4-(4-Chlorobenzoyl)benzyl]-3-propyl-7H-pyrrolo-[2,3-d]pyrimidin-4-one

https://huagongshe.com/reaction/1291397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(4-Chlorobenzoyl)benzyl bromideHCID 9839651—
Reactant3-propyl-7H-pyrrolo[2,3-d]pyrimidin-4-oneHCID 18918872—
Solvent1,2-DimethoxyethaneHCID 8071—
Product7-[4-(4-Chlorobenzoyl)benzyl]-3-propyl-7H-pyrrolo-[2,3-d]pyrimidin-4-oneHCID 1891918488.9%

Reaction Steps

Under argon gas, 3-propyl-7H-pyrrolo[2,3-d]pyrimidin-4-one (249 mg) was dissolved in anhydrous DME (6 ml) and, under ice-cooling and stirring, 60% sodium hydride-oil (62 mg) was added. The mixture was stirred for 30 minutes, after which a solution of 4-(4-chlorobenzoyl)benzyl bromide (564 mg) in anhydrous DME (2 ml) was added. The mixture was further stirred at room temperature for 2 hours. The solvent was then distilled off under reduced pressure and the residue was dissolved in ethyl acetate, washed with saturated aqueous NaCl solution, and dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure and the residue was purified by flash column chromatography (silica gel, 21 g; hexane: ethyl acetate =4:1-3:2) to provide the title compound as colorless powder (507 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-288e65d9ae444ff9999673be74ab677b
Source noteuspto-grants-1998_05