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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74459생성일: 2026년 10월 24일

Toluene → 6-cyclopropyl-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/74459

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Cesium carbonateHCID 10796—
반응물Di-tert-butylphenylphosphineHCID 316378—
반응물6-bromo-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl esterHCID 68004810—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물6-cyclopropyl-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl esterHCID 68004830—

반응 조건

온도100 °C

반응 단계

Predetermined amounts of 6-bromo-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl ester (300 mg, 0.73 mmol), palladium acetate (16.5 mg, 0.07 mmol), bis(1,1-dimethylethyl)phenylphosphine (0.028 ml, 0.12 mmol), potassium cyclopropyl trifluoroborate (163 mg, 1.1 mmol), and cesium carbonate (718 mg, 2.2 mmol) were placed in a reaction container, and toluene (5 ml) and water (0.5 ml) were added thereto. The resulting mixture was then stirred at 100° C. for 14 hours. After cooling it to room temperature, the mixture was diluted with ethyl acetate, and washed twice with water, and then dried over anhydrous sodium sulfate. The desiccant was removed by filtration, and concentration was performed. Then, the residue obtained by concentration under reduced pressure was purified by silica gel column chromatography (hexane/ethyl acetate=97/3 to 7/3). Thus, a yellow solid was obtained (208 mg, 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829199B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-fb17bd2a5fb640e9b9ec8cb20bfeb4f5
출처 메모uspto-grants-2014_09