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Triethylamine → 5-[3-(Phthalimido)propylthio]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 | N-3-Bromopropylphthalimide | HCID 21611 | — |
| 反応物 | HCID 178418687 | HCID 178418687 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-[3-(Phthalimido)propylthio]imidazo[1,2-a]pyridine | HCID 23362941 | 71.1% |
反応手順
To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (3.00g, 20 mmoles) and N-[3-(bromo)propyl]phthalimide (5.90 g, 22 mmoles) in ethanol (200 ml) was added triethylamine (4.2 ml, 30 mmoles) and the mixture was stirred at room temperature for 1 hour and heated at reflux for 1 hour. After the solvent was distilled off, chloroform was added to the residue, which was washed with water, dried over anhydrous magnesium sulfate and the solvent was distilled off. Then, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 4.79 g of the desired product (71.1%, colorless 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-2142af33e93641faaf0996e15f201439 |
| 出典メモ | uspto-grants-1993_09 |