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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1786925Erstellt: 24. Oktober 2026

N-methyl-2-pyrrolidone → N-[4-(benzyloxy)-3-chlorophenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amine

https://huagongshe.com/de/reaction/1786925

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-methyl-2-pyrrolidoneHCID 13387—
Edukt4-Benzyloxy-3-chloroanilineHCID 1268285—
Edukt4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
LösungsmittelMethanolHCID 887—
ProduktN-[4-(benzyloxy)-3-chlorophenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amineHCID 5759727149,5%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (200 mg), 4-(benzyloxy)-3-chloroaniline (365 mg) and 1-methyl-2-pyrrolidone (3 mL) was stirred at 80° C. for 4 hrs. Methanol and activated carbon were added to the reaction mixture and the mixture was stirred. The activated carbon was filtered off, aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent, methanol:ethyl acetate=0:100→15:75) and recrystallized from ethanol-ethyl acetate to give the title compound (226 mg) as a pale-brown powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07507740B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-69cd76e25f794ae5ae52dfdfac3d9ec8
Quellennotizuspto-grants-2009_03