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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64873Erstellt: 23. Oktober 2026

Oxalic Acid → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(4-fluorophenyl)piperazine oxalate

https://huagongshe.com/de/reaction/64873

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalic AcidHCID 971—
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt1-(4-Fluorophenyl)piperazineHCID 75260—
Edukt3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(4-fluorophenyl)piperazine oxalateHCID 13520733—

Reaktionsschritte

A mixture of 5.0 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 4.0 g of 1-(4-fluorophenyl)piperazine, 10 g of potassium carbonate and a few crystals potassium iodide in 70 ml of dimethylformamide was stirred at 80° C. for 4.5 hr. The mixture was cooled, filtered and concentrated to an oil, which was stirred with water and extracted with ethyl acetate-ether. The organic extracts were washed with water (2×), saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture was filtered and concentrated. The residue was purified by column chromatography (silica gel, tetrahydrofuran) to give an oil. The oil was converted to 4.5 g (45%) of product by treatment with oxalic acid. Two recrystallizations from ethyl acetate/methanol gave the analytical sample, mo 186°-187° C. (dec).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04610988
Quelldatensatzuspto-grants-1986_09
ORD IDord-ab3f0d82e4be403ea50296641c73b690
Quellennotizuspto-grants-1986_09