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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1851Erstellt: 24. Oktober 2026

2-Methylpiperazine → Ethyl 1-ethyl-8-(3-methyl-1-piperazinyl)-4H-quinolizin-4-one-3-carboxylate

https://huagongshe.com/de/reaction/1851

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethylpiperazineHCID 66057—
EduktEthyl 8-chloro-1-ethyl-4-oxo-4H-quinolizine-3-carboxylateHCID 10660349—
LösungsmittelPyridineHCID 1049—
ProduktEthyl 1-ethyl-8-(3-methyl-1-piperazinyl)-4H-quinolizin-4-one-3-carboxylateHCID 19691415100,5%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

Ethyl 8-chloro-1-ethyl-4H-quinolizin-4-one-3-carboxylate (558 mg, 2.0 mmol), the product of Step 3 of Example 62, was dissolved in 10 mL of dry pyridine under a nitrogen atmosphere. To the resultant solution was added 600 mg (6.0 mmol) of 2-methylpiperazine and the stirred reaction mixture was heated at 65° C. for 3 hours. The reaction mixture was allowed to cool to ambient temperature and then concentrated in vacuo in order to remove all of the pyridine. The residue was dissolved in 60 mL of methylene chloride and the methylene chloride solution was washed with 60 mL of water. The aqueous layer was extracted with 2 X 60 mL of methylene chloride and the combined methylene chloride solutions were dried over anhydrous sodium sulfate, filtered and concentrated and dried in vacuo to afford 690 mg of the title compound. The product was carried on to the next step without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726182
Quelldatensatzuspto-grants-1998_03
ORD IDord-dbb3e314646f42c4828e49ee8c678c63
Quellennotizuspto-grants-1998_03