化工社化工社 化学情報印刷レポート · 研究参考用
Acetonitrile → 5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Benzenesulfonyl chloride | HCID 7369 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 5-[3-(Amino)propyloxy]imidazo[1,2-a]pyridine dihydrochloride | HCID 23362997 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridine | HCID 23362978 | 59.5% |
反応手順
To a suspension of 5-[3-(amino)propyloxy]imidazo[1,2-a]pyridine dihydrochloride (2.64 g, 10 mmoles) and triethylamine (4.88 ml, 35 mmoles) in methylene chloride (100 ml)-acetonitrile (30 ml) was added benzenesulfonyl chloride (1.53 ml, 12 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 saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the crude product thus obtained was recrystallized from methylene-ethanol to obtain 1.97 g of the desired product (59.5%, light brown crystals).
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-87ae7e60b3f94aeab00f82581b06295a |
| 出典メモ | uspto-grants-1993_09 |