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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1281746생성일: 2026년 10월 26일

Piperidine → 4-[(1-Methyl-4-phenylindol-3-yl)methylene]-3-pyridino[3,4-e]pyridin-2-yl-2-pyrazolin-5-one

https://huagongshe.com/reaction/1281746

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물PyrazoloneHCID 11513733—
반응물5,6-Methylenedioxy-1-methyl-indole-3-carboxaldehydeHCID 22605371—
용매EthanolHCID 702—
생성물4-[(1-Methyl-4-phenylindol-3-yl)methylene]-3-pyridino[3,4-e]pyridin-2-yl-2-pyrazolin-5-oneHCID 6991947459%

반응 조건

온도87.5 °C

반응 단계

A mixture of the above pyrazolone, (VIk) (10 mg, 0.047 mmol), 5,6-methylenedioxy-1-methyl-indole-3-carboxaldehyde (11 mg, 0.054 mmol) in 1 mL of absolute ethanol along with a drop of piperidine was kept under stirring at 85-90° C. A solid separated. After 2 h the mixture was cooled to room temperature and the solid was filtered, washed with ethanol and dried to isolate the product (11 mg, 59% yield). MS: 398 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06455525B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-c1b96b907ba44ef68f1cd2c95ace8609
출처 메모uspto-grants-2002_09