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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233906Erstellt: 25. Oktober 2026

Decanoyl chloride → Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochloride

https://huagongshe.com/reaction/233906

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDecanoyl chlorideHCID 66982—
EduktSodium BicarbonateHCID 516892—
Edukt6-Fluoro-3-[1-(3-hydroxy-3-ethylpentyl)4-piperidinyl]-1,2-benzisoxazoleHCID 18467342—
LösungsmittelDichloromethaneHCID 6344—
ProduktDecanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochlorideHCID 8674976081%

Reaktionsschritte

To a solution of 6-fluoro-3-[1(3-hydroxy-3-ethylpentyl)-4-piperidinyl]-1,2-benzisoxazole (2.5 g, 7.48 mmol) in DCM (100 ml) was added decanoyl chloride (1.5 ml, 7.48 mmol) at 0° C., under nitrogen. The reaction mixture was stirred for 4 days at which time it was poured into NaHCO3 (sat., 50 ml). The layers were separated and the aqueous phase was extracted with DCM (2×). The combined organics were dried, filtered and concentrated to give the crude product which was purified via flash column chromatography (silica gel, 20-40% EtOAc/DCM). The product containing fractions were concentrated to give 3.0 g (81%) of the desired product as a yellow oil. The hydrochloride salt was prepared in anhydrous ether (60 ml) and isopropanol (1 ml) with ethereal HCl. The white salt was filtered and washed with anhydrous ether, m.p.=159°-161° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05593995
Quelldatensatzuspto-grants-1997_01
ORD IDord-2248463d413b49e0b9ae51dc80b43189
Quellennotizuspto-grants-1997_01