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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1372131Erstellt: 26. Oktober 2026

7-Nitroindazole → 1-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-[7-nitro-indazol-1-yl]-ethanone

https://huagongshe.com/reaction/1372131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt7-NitroindazoleHCID 1893—
EduktPotassium CarbonateHCID 11430—
Edukt1-(Chloroacetyl)-4-(4-fluorophenyl)piperazineHCID 1848511—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[4-(4-Fluoro-phenyl)-piperazin-1-yl]-2-[7-nitro-indazol-1-yl]-ethanoneHCID 21071011—

Reaktionsschritte

2-Chloro-1-[4-(4-fluoro-phenyl)-piperazin-1-yl]-ethanone (0.834 g, 3.3 mmol) was taken in dry DMF (15 mL) and dry potassium carbonate (1.6 g, 11.6 mmol) was added to it and the reaction mixture stirred at room temperature for 1 h under nitrogen. 7-Nitro-1H-indazole (0.5 g, 2.9 mmol) in DMF (2 mL) was then added to the mixture through a syringe. The reaction was then heated at 70° C. for 14 h, cooled and then quenched with water and extracted with ethyl acetate. Drying of the organic layer with Na2SO4 followed by concentration afforded material that was purified on neutral alumina column (pet ether/ethyl acetate). The resulting solid was recrystallized from DCM/pet ether to obtain pure product as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157464B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-1cd1bd052fb6497594fc50203ce25e3b
Quellennotizuspto-grants-2007_01