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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1860935생성일: 2026년 10월 26일

Oxindole → 4-(2-Methoxycarbonyl-ethyl)-3-methyl-5-(2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1860935

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참여 물질

역할이름HCID투입량
반응물OxindoleHCID 321710—
반응물5-(Ethoxycarbonyl)-2-formyl-4-methyl-1H-pyrrole-3-propanoic Acid Methyl EsterHCID 15533557—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물4-(2-Methoxycarbonyl-ethyl)-3-methyl-5-(2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid ethyl esterHCID 5377729375.1%

반응 조건

온도10 °C

반응 단계

5-Formyl-4-(2-methoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (80.2 g), 2-oxindole (37.9 g) and ethanol (300 mL) were warmed to 70° C. in a 500 mL, 3-neck round bottom flask equipped with mechanical stirring and a reflux condenser. Piperidine (1.3 g) was added and the mixture was refluxed for 4 hours. The mixture was cooled to 10° C. and the orange precipitate collected by vacuum filtration and washed with 30 mL of ethanol. The solid was slurry-washed in 150 mL of refluxing ethanol, cooled, collected by vacuum filtration, washed with 30 mL of ethanol and vacuum dried to give 81.7 g (75%) of 4-(2-Methoxycarbonylethyl)-3-methyl-5-(2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid ethyl ester as an orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06531502B1
출처 데이터셋uspto-grants-2003_03
ORD IDord-9d84529eeb5e4d67a74832536e51017c
출처 메모uspto-grants-2003_03