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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264209Erstellt: 24. Oktober 2026

Potassium Carbonate → 4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl acetate fumarate

https://huagongshe.com/de/reaction/264209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt1-Butanol, 4-bromo-, 1-acetateHCID 78491—
EduktFumaric AcidHCID 444972—
Edukt3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
LösungsmittelEthanolHCID 702—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl acetate fumarateHCID 21960104—

Reaktionsschritte

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (9.5 g, 41 mmol), K2CO3 (7.2 g, 51 mmol), and 4-bromobutyl acetate (10 g, 51 mmol) in acetonitrile (200 ml) was heated at reflux for 3.5 hours. At the end of the reaction, the solution was cooled and filtered. The inorganic salt was washed with DCM (50 ml). The organic solvent was removed. The residue was purified on a flash chromatography column (packed with Sorbsil C30 silica gel, 100 g, eluted with DCM, 1 liter, increasing methanol from 2 to 4%, 2.51). The material thus purified weighed 12.92 g (89%). A small sample (1.67 g) was dissolved in ethanol and treated with 1 equivalent of fumaric acid (580 mg) in ethanol to yield white crystals: 1.8 g, m.p.=142°-143° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646161
Quelldatensatzuspto-grants-1997_07
ORD IDord-44a220d228d64e819471821c362d14e0
Quellennotizuspto-grants-1997_07