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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 6-Methoxyoxindole | HCID 2793749 | — |
| 반응물 | 5-Formyl-4-(2-ethoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester | HCID 11022333 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 4-(2-carboxyethyl)-3-methyl-5-(6-methoxy-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid | HCID 53690322 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06855730B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-af289579989748c1aca026cdf56f41e5 |
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| 출처 메모 | uspto-grants-2005_02 |
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