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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1634180Erstellt: 27. Oktober 2026

Ethyl 4-oxo-1-piperidinecarboxylate → ethyl 1,3,4,5-tetrahydro-8-(phenylmethoxy)-2H-pyrido[4,3-b]indole-2-carboxylate

https://huagongshe.com/reaction/1634180

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
Edukt4-BenzyloxyphenylhydrazineHCID 561392—
LösungsmittelEthanolHCID 702—
Produktethyl 1,3,4,5-tetrahydro-8-(phenylmethoxy)-2H-pyrido[4,3-b]indole-2-carboxylateHCID 1867741663,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of ethyl 4-oxo-1-piperidinecarboxylate (0.23 mol) and 4-(benzyloxy)-phenyl hydrazine (0.23 mol) in ethanol (400 ml) was stirred and refluxed for 5 hours. The reaction mixture was stirred overnight at room temperature. The solid was filtered off and washed on filter with H2O/2-propanol (200 ml). The precipitate was dissolved in CHCl3 (300 ml), washed with water (2×50 ml), dried, filtered and the solvent was evaporated. The residue was crystallized from CH3CN (300 ml) and cooled to 0° C. The resulting precipitate was filtered off and dried, yielding 51.0 g (63%) of ethyl 1,3,4,5-tetrahydro-8-(phenylmethoxy)-2H-pyrido[4,3-b]indole-2-carboxylate (intermediate 1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06506768B2
Quelldatensatzuspto-grants-2003_01
ORD IDord-4fcb784bbd514a9490ecda8ef8405621
Quellennotizuspto-grants-2003_01