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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24538생성일: 2026년 10월 24일

Piperidine → 4-(2-carboxyethyl)-3-methyl-5-(6-methoxy-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid

https://huagongshe.com/ko/reaction/24538

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Potassium HydroxideHCID 14797—
반응물6-MethoxyoxindoleHCID 2793749—
반응물5-Formyl-4-(2-ethoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl esterHCID 11022333—
용매EthanolHCID 702—
생성물4-(2-carboxyethyl)-3-methyl-5-(6-methoxy-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acidHCID 5369032299%

반응 조건

온도95 °C

반응 단계

5-Formyl-4-(2-ethoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (591 mg), 6-methoxy-2-oxindole (333 mg) and piperidine (0.1 mL) in ethanol (4 mL) were stirred at 90° C for 2 hours. Potassium hydroxide (537 mg) was added to the mixture and it was then stirred at 95° C. for and additional hour. The reaction mixture was cooled and concentrated, dissolved in water, and acidified with 2 N hydrochloric acid to pH 2. The precipitate was filtered, washed with water, and dried in a vacuum oven overnight to give 730 mg (99%) of 4-(2-carboxyethyl)-3-methyl-5-(6-methoxy-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-af289579989748c1aca026cdf56f41e5
출처 메모uspto-grants-2005_02