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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55645Erstellt: 23. Oktober 2026

Potassium Carbonate → 1-(3-Dimethylaminopropyl)-4-(6-fluoro-1,2-benzisoxazol-yl)piperidine difumarate

https://huagongshe.com/de/reaction/55645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt3-(Dimethylamino)propyl chloride hydrochlorideHCID 94308—
EduktFumaric AcidHCID 444972—
Edukt3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-(3-Dimethylaminopropyl)-4-(6-fluoro-1,2-benzisoxazol-yl)piperidine difumarateHCID 6707110056,9%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.05 g, 13.8 mmol), 3-dimethylaminopropyl chloride hydrochloride (3.4 g, 21 mmol), K2CO3 (6.2 g, 45 mmol), tetrabutylammonium hydrogen sulfate (phase transfer catalyst, 1.5 g) in acetonitrile (100 ml) and water (50 ml) was heated at 60° C. overnight. The aqueous phase was separated, and acetonitrile was removed at reduced pressure. The residue was extracted into DCM. The organic solution was washed with H2O and brine, then dried with MgSO4. The solvent was removed and the crude product (4.3 g) was treated with fumaric acid (1.58 g, 1.0 eq) in dilute ethanol. The crystals were collected (2.53 g), m.p.=192°-194° C. Recrystallization from ethanol yielded 2.08 g of white crystals, mp=194°-195° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624927
Quelldatensatzuspto-grants-1997_04
ORD IDord-abf3cdd92c534119b808c05d65a1a1c9
Quellennotizuspto-grants-1997_04