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Potassium tert-butoxide → 4-Bromo-6-(trifluoromethyl)-1H-indole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | 3-Bromo-2-ethynyl-5-(trifluoromethyl)benzenamine | HCID 57546030 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 4-Bromo-6-(trifluoromethyl)-1H-indole | HCID 24729231 | 69.2% |
反応手順
To a solution of potassium tert-butoxide (1.33 g) in NMP (30 mL) was added a solution of 3-bromo-2-ethynyl-5-(trifluoromethyl)aniline (1.56 g) in NMP (5 mL) at 0° C., and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous ammonium chloride solution, water and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane) to give the title compound (1.08 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09296746B2 |
| 出典データセット | uspto-grants-2016_03 |
| ORD ID | ord-3f300523527b44a7b1af5fe32608213b |
| 出典メモ | uspto-grants-2016_03 |