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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280896Erstellt: 24. Oktober 2026

Potassium Carbonate → 4-Cyano-1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-phenylpiperidine hydrochloride

https://huagongshe.com/de/reaction/280896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-Phenylpiperidine-4-carbonitrile hydrochlorideHCID 3084973—
Edukt3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
KatalysatorPotassium IodideHCID 4875—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Cyano-1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-phenylpiperidine hydrochlorideHCID 1331987230,4%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To 50 ml of dimethylformamide was added 4.4 g of 4-cyano-4-phenylpiperidine hydrochloride, 6.4 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 10 g of milled potassium carbonate, and 0.01 g of potassium iodide. After stirring at 90° C. for three hrs, the mixture was cooled, filtered, and the filtrate was evaporated to an oil. The oil was stirred with 100 ml of water for ten mins and then extracted with ether. The ether solution was washed with water (2x), saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, the solvent was evaporated. The residue was filtered through a silica gel column with tetrahydrofuran. The eluant was evaporated to an oil. The oil was dissolved in ether and treated with ethereal hydrogen chloride to give 2.4 g (29%) of product, mp 235° C. (dec). Recrystallization from ethyl acetate/methanol gave the analytical sample, mp 239° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04591586
Quelldatensatzuspto-grants-1986_05
ORD IDord-0b413f610e0e4919aca5324749640a11
Quellennotizuspto-grants-1986_05