Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74456생성일: 2026년 10월 24일
2-(ethoxycarbonyl)-1-tosyl-1H-indole-5-carboxylic acid → 1-(toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 5-tert-butyl ester 2-ethyl ester
https://huagongshe.com/ko/reaction/74456
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-(ethoxycarbonyl)-1-tosyl-1H-indole-5-carboxylic acid | HCID 68004853 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | 1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine | HCID 547712 | — |
| 생성물 | 1-(toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 5-tert-butyl ester 2-ethyl ester | HCID 68005321 | 134.3% |
반응 단계
1-(Toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 2-ethyl ester (690 mg, 1.85 mmol) was dissolved in N,N-dimethylformamide di-tert-butyl acetal (3.0 ml), and stirred at 80° C. for two and half hours. N,N-dimethylformamide di-tert-butyl acetal (2.0 ml) was further added thereto and stirred at 80° C. for three hours. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate (150 ml) and water (75 ml). The organic layer was isolated, washed with water and a saturated aqueous solution of sodium chloride, and then dried over anhydrous sodium sulfate. The desiccant was removed by filtration. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=25/1 to 5/1) to give 1-(toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 5-tert-butyl ester 2-ethyl ester (551 mg, 69%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08829199B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-07437c96346649d795b3ab596e77bf25 |
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| 출처 메모 | uspto-grants-2014_09 |
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