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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 469322Erstellt: 24. Oktober 2026

Tetrahydrofuran → 1-Benzyl-4-(2-chloro-6-methoxyquinolin-3-yl)piperidin-4-ol

https://huagongshe.com/de/reaction/469322

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt2-Chloro-6-methoxyquinolineHCID 83647—
EduktLithium diisopropylamideHCID 2724682—
Edukt1-Benzyl-2-piperidoneHCID 5170076—
Produkt1-Benzyl-4-(2-chloro-6-methoxyquinolin-3-yl)piperidin-4-olHCID 58181126—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Under an argon atmosphere 14.0 mL (28.0 mmol) of a 2 M lithium diisopropylamide solution in 50 mL THF were cooled to −78° C. and combined with stirring with a solution of 5.00 g (25.1 mmol) of 2-chloro-6-methoxy-quinoline in THF. After 1 h stirring at −78° C., 4.5 mL (25.2 mmol) N-benzylpiperidone were added dropwise. After 1 h stirring at −78° C. the mixture was allowed to come up to RT and stirred overnight. The mixture was evaporated down i. vac. and purified by flash chromatography through Alox. The fractions containing the product were combined and evaporated down.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629137B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-86951bac4dce423987c5afaee4886243
Quellennotizuspto-grants-2014_01