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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

반응식

참여 물질

역할이름HCID투입량
반응물2-(ethoxycarbonyl)-1-tosyl-1H-indole-5-carboxylic acidHCID 68004853—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
생성물1-(toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 5-tert-butyl ester 2-ethyl esterHCID 68005321134.3%

반응 조건

온도80 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829199B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-07437c96346649d795b3ab596e77bf25
출처 메모uspto-grants-2014_09