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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17871Erstellt: 24. Oktober 2026

Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate → Benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/de/reaction/17871

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270—
Edukt2-Benzyl-4-methoxy-N-methylbenzamideHCID 22555927—
EduktIsopropanol carbon dioxideHCID 86586944—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl acetate hexaneHCID 21226206—
ProduktBenzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylateHCID 6843349049,4%

Reaktionsschritte

To an isopropanol/dry ice cooled solution of 4-Methoxy-N-methyl-2-(phenylmethyl)benzamide (250 mg, 0.980 mmol) in THF (50 mL) under argon was added sec-butyllithium solution (1.3M, 1.55 mL, 2.00 mmol) dropwise. After 10 min. a THF (10 mL) solution of benzyl-4-(chlorocarbonyl)piperidine-1-carboxylate (275 mg, 980 mmol) was quickly added to the reaction solution. After 10 min. the reaction was quenched with water then warmed to room temperature. Saturated sodium bicarbonate was added and the resulting mixture extracted with ethyl acetate (3×) and dried with anhydrous magnesium sulfate. Filtration followed by evaporation of solvent in vacuo gave the crude product which was subjected to flash column chromatography (hexane:ethyl acetate 50:50) to afford benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate as a white foam (242 mg, 0.484 mmol, 49%). MS [M+H]+ 501.2

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741322B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-cdf90ed4d8804be8853d1f11965f5421
Quellennotizuspto-grants-2010_06