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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1516822Erstellt: 25. Oktober 2026

3,5-Dimethyl-4-hydroxybenzonitrile → 4-(2-amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile

https://huagongshe.com/reaction/1516822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-Dimethyl-4-hydroxybenzonitrileHCID 20176—
EduktSodium hydrideHCID 24758—
Edukt7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amineHCID 10587340—
Lösungsmittel1-Methyl-2(1H)-pyridinoneHCID 12755—
Produkt4-(2-amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrileHCID 5769357583%

Reaktionsschritte

To a solution of 4-hydroxy-3,5-dimethylbenzonitrile (1.62 mg, 11.0 mmol) in 1-methyl-2-pyridone (5 mL) in a sealed tube was added NaH (441 mg, 11.0 mmol). The reaction mixture was stirred at room temperature for 15 min and a solution of 7-benzyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine (950 mg, 3.67 mmol) in 1-methyl-2-pyridone (5 mL) was added to the mixture. The mixture was heated at 150° C. for 16 h and cooled to room temperature. The reaction was poured into ice water and extracted with EtOAc (2×50 mL). The combined organic solution was washed with H2O (50 mL) and brine (50 mL), dried with Na2SO4, and concentrated to dryness. Silica gel chromatography (Hexanes:EtOAc=75:25) yielded 1.12 mg (83%) of 4-(2-amino-7-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-yloxy)-3,5-dimethyl-benzonitrile.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08227601B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-d1f8828889b14cc59b26ef2bafa8f023
Quellennotizuspto-grants-2012_07