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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233207Erstellt: 24. Oktober 2026

Decanoyl chloride → 3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl decanoate fumarate

https://huagongshe.com/de/reaction/233207

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDecanoyl chlorideHCID 66982—
EduktFumaric AcidHCID 444972—
Edukt3-(4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl)propan-1-olHCID 15384966—
LösungsmittelEthanolHCID 702—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl decanoate fumarateHCID 21960039—

Reaktionsschritte

To a solution 3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propanol (1.81 g, 6.5 mmol) triethylamine (0.9 g, 9.0 mmol) in DCM (45 ml) was added decanoyl chloride (1.5 g, 7.8 mmol) dropwise at room temperature. The mixture was stirred for 20 minutes, then concentrated down to a crude solid. The solid was extracted into EtOAc (20 ml), and the insoluble salts were filtered. The EtOAc was removed. The crude oil was purified by flash choursomatography (Sorbsil C-30, 30 g; eluted with MeOH:DCM). The oil thus obtained (2.54 g, 90%) was converted to a fumarate salt with fumaric acid (670 mg) in ethanol. The crystals collected weighed 1.61 g, m.p.=100°-102° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591745
Quelldatensatzuspto-grants-1997_01
ORD IDord-5dfba5e8f1d144d699a38d748b772de9
Quellennotizuspto-grants-1997_01