Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24542생성일: 2026년 10월 25일
Potassium Hydroxide → 4-(2-carboxy-ethyl)-3-methyl-5-(6-chloro-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid
https://huagongshe.com/reaction/24542
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 6-Chloro-1,3-dihydroindol-2-one | HCID 736344 | — |
| 반응물 | 5-Formyl-4-(2-ethoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester | HCID 11022333 | — |
| 촉매 | Piperidine | HCID 8082 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 4-(2-carboxy-ethyl)-3-methyl-5-(6-chloro-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid | HCID 54056821 | 72.1% |
반응 단계
5-Formyl-4-(2-ethoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (281 mg), 6-chloro-2-oxindole (168 mg) and piperidine (2 drops) in ethanol (2 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. The residue was dissolved into 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 270 mg (72%) of 4-(2-carboxy-ethyl)-3-methyl-5-(6-chloro-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-042d9cd96a0c48a09b15ba2e59c395ff |
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| 출처 메모 | uspto-grants-2005_02 |
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