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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513846생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/513846

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 trifluoro borate (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 번호US09102692B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-b73532bf65374dffad1e8f116518cd41
출처 메모uspto-grants-2015_08