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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2381676Erstellt: 26. Oktober 2026

Water → 1-(4-(4-(4-(methylthio)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone

https://huagongshe.com/reaction/2381676

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktChlorotrimethylsilaneHCID 6397—
Edukt1-[4-(4-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 736269—
Edukt2-chloro-4-(methylthio)-7H-pyrrolo[2,3-d]pyrimidineHCID 57990275—
Lösungsmittel1-ButanolHCID 263—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(4-(4-(4-(methylthio)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanoneHCID 6902313748,7%

Reaktionsbedingungen

Temperatur116 °C

Reaktionsschritte

A mixture of 2-chloro-4-(methylthio)-7H-pyrrolo[2,3-d]pyrimidine (484 mg, 2.43 mmol), 1-(4-(4-aminophenyl)piperazin-1-yl)ethanone (645 mg, 2.95 mmol) and trimethylsilyl chloride (0.500 mL, 3.95 mmol) in nBuOH (10 mL) was heated at 116° C. for 48 h. After cooling down, H2O and EtOAc were added. The organic phase was separated, washed with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo to give 1-(4-(4-(4-(methylthio)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone as a solid (453 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08258144B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-9ab068c6bbaa4934b1646ed25d2749af
Quellennotizuspto-grants-2012_09