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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1847Erstellt: 23. Oktober 2026

1-Methylpiperazine → Ethyl 8-(4-methylpiperazin-1-yl)-4H-quinolizin-4-one-3-carboxylate

https://huagongshe.com/de/reaction/1847

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylpiperazineHCID 53167—
EduktEthyl 8-chloro-4-oxo-4H-quinolizine-3-carboxylateHCID 3314858—
LösungsmittelPyridineHCID 1049—
ProduktEthyl 8-(4-methylpiperazin-1-yl)-4H-quinolizin-4-one-3-carboxylateHCID 15389003106,8%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Ethyl 8-chloro-4H-quinolizin-4-one-3-carboxylate (755 mg, 3.0 mmol), the product of Step 3 of Example 58, was suspended in 12 mL of dry pyridine under a nitrogen atmosphere. To the resultant solution was added 6.0 mL (6.0 mmol) of N-methylpiperazine and the reaction mixture was heated at 70° C. for 8 hours. The reaction mixture was then concentrated in vacuo in order to remove all of the pyridine. The dry residue (3.124 g) was dissolved in 125 mL of methylene chloride and the methylene chloride solution was washed with 125 mL of saturated sodium chloride solution (brine). The aqueous layer was extracted with 125 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 1.01 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726182
Quelldatensatzuspto-grants-1998_03
ORD IDord-d1417262cbeb4dcfb27be135b8b405b2
Quellennotizuspto-grants-1998_03