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Triethylamine → 5-[4-(1-Naphthalenesulfonylamino)butylthio]imidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-Naphthalenesulfonyl chloride | HCID 66560 | — |
| 反応物 | 5-[4-(Amino)butylthio]imidazo[1,2-a]pyridine | HCID 23362894 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-[4-(1-Naphthalenesulfonylamino)butylthio]imidazo[1,2-a]pyridine | HCID 23362885 | 53.3% |
反応手順
To a solution of 5-[4-(amino)butylthio]imidazo[1,2-a]pyridine (300 mg, 1.36 mmoles) and triethylamine (0.29 ml, 2.08 mmoles) in methylene chloride (15 ml) was added 1-naphthalenesulfonyl chloride (307 mg, 1.35 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous sodium bicarbonate solution and water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 296 mg of the desired product (53.0%, colorless solid).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05244908 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-60c2ecf6995d45a5aa4ac142f572040a |
| 出典メモ | uspto-grants-1993_09 |