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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55667Erstellt: 23. Oktober 2026

Triethylamine → 4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]2-methylbutyl decanoate fumarate

https://huagongshe.com/de/reaction/55667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDecanoyl chlorideHCID 66982—
EduktFumaric AcidHCID 444972—
Edukt4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]-2-methyl-2-butanolHCID 18467367—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
Produkt4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]2-methylbutyl decanoate fumarateHCID 18467288—

Reaktionsschritte

To a mixture of 4-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-2-methyl-2-butanol (4.68 g, 15.3 mmol) and triethylamine (2.23 g, 22.3 mmol) in chloroform (20 ml) was added decanoyl chloride (3.5 g, 18.4 mmol, 1.2 eq) dropwise at 0° C. The reaction was stirred at ambient temperature for 4 hours. The solvent was removed. The residue was purified by flash chromatography over a silica gel column (SiO2, 65 g, eluted with DCM, 1 l, 1% CH3OH in DCM, 1 l). The product thus purified weighed 5.7 g (80%) as an oil. This oily product was converted to the fumarate salt in ethanol with fumaric acid (1.51 g, 1.0 eq) to yield 3.34 g, m.p.=133°-134° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624927
Quelldatensatzuspto-grants-1997_04
ORD IDord-b049f85696314ef780311e08fe8def42
Quellennotizuspto-grants-1997_04