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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1291398Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1291398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt4-(4-Chlorobenzoyl)benzyl bromideHCID 9839651—
Edukt3-Isopropyl-7H-pyrrolo[2,3-d]pyrimidin-4(3H)-oneHCID 18919040—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt7-[4-(4-Chlorobenzoyl)benzyl]-3-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-4-oneHCID 1891886688,8%

Reaktionsschritte

Under argon gas, 3-isopropyl-7H-pyrrolo[2,3-d]-pyrimidin-4-one (89 mg) was dissolved in anhydrous DME (2 ml) and, under ice-cooling and stirring, 60% sodium hydride-oil (22 mg) was added. The mixture was stirred for 30 minutes, after which a solution of 4-(4-chlorobenzoyl)benzyl bromide (201 mg) in anhydrous DME (1 ml) was added. Then, the mixture was stirred at room temperature for 2 hours. The solvent was 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, 12 g; hexane: ethyl acetate =4:1-3:2) to provide the title compound as colorless powder (181 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05753664
Quelldatensatzuspto-grants-1998_05
ORD IDord-a1aa45ffbd484eaaa858da39786848ea
Quellennotizuspto-grants-1998_05