化工社化工社 化学情報印刷レポート · 研究参考用
p-Anisoyl chloride → Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Anisoyl chloride | HCID 7477 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ethyl 3-amino-1H-indole-2-carboxylate | HCID 732887 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylate | HCID 751363 | 94.1% |
反応手順
To a solution of 3-amino-2-indolecarboxylic acid ethyl ester (500 mg, 2.45 mmol) and triethylamine (272 mg, 2.70 mmol) in methylene chloride (5 mL) was added anisoyl chloride (418 mg, 2.45 mmol). The resulting mixture was stirred for 18 h at room temperature. The reaction mixture was diluted with ethyl acetate and washed with water. The organic phase was washed with 1 N aqueous hydrochloric acid, dried (sodium sulfate), filtered, and concentrated in vacuo to provide a yellow solid. Recrystallization from hexane/ethyl acetate provided 780 mg (94%) of the title compound as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06313151B1 |
| 出典データセット | uspto-grants-2001_11 |
| ORD ID | ord-733b89533ee64034b26e3ebb33f90f79 |
| 出典メモ | uspto-grants-2001_11 |