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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1847생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물Ethyl 8-chloro-4-oxo-4H-quinolizine-3-carboxylateHCID 3314858—
용매PyridineHCID 1049—
생성물Ethyl 8-(4-methylpiperazin-1-yl)-4H-quinolizin-4-one-3-carboxylateHCID 15389003106.8%

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726182
출처 데이터셋uspto-grants-1998_03
ORD IDord-d1417262cbeb4dcfb27be135b8b405b2
출처 메모uspto-grants-1998_03