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HRID 74459作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Cesium carbonateHCID 10796—
反応物Di-tert-butylphenylphosphineHCID 316378—
反応物6-bromo-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl esterHCID 68004810—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物6-cyclopropyl-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl esterHCID 68004830—

反応条件

温度100 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829199B2
出典データセットuspto-grants-2014_09
ORD IDord-fb17bd2a5fb640e9b9ec8cb20bfeb4f5
出典メモuspto-grants-2014_09