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HRID 1847作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylpiperazineHCID 53167—
反応物Ethyl 8-chloro-4-oxo-4H-quinolizine-3-carboxylateHCID 3314858—
溶媒PyridineHCID 1049—
生成物Ethyl 8-(4-methylpiperazin-1-yl)-4H-quinolizin-4-one-3-carboxylateHCID 15389003106.8%

反応条件

温度70 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726182
出典データセットuspto-grants-1998_03
ORD IDord-d1417262cbeb4dcfb27be135b8b405b2
出典メモuspto-grants-1998_03