関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Di-tert-butylphenylphosphine | HCID 316378 | — |
| 反応物 | 6-bromo-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl ester | HCID 68004810 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 6-cyclopropyl-1-(toluene-4-sulfonyl)-1H-indole-2-carboxylic acid methyl ester | HCID 68004830 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829199B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-fb17bd2a5fb640e9b9ec8cb20bfeb4f5 |
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| 出典メモ | uspto-grants-2014_09 |
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