化工社化工社 化学情報印刷レポート · 研究参考用
2-Trifluoromethylbenzenesulphonyl chloride → ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Trifluoromethylbenzenesulphonyl chloride | HCID 136616 | — |
| 反応物 | 1H-Indole-2-carboxylic acid, 7-amino-, ethyl ester | HCID 11138194 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylate | HCID 57476178 | 88.2% |
反応手順
To a mixture of ethyl 7-amino-1H-indole-2-carboxylate (4.1 g) and pyridine (60 mL) was added 2-trifluoromethylbenzenesulfonyl chloride (5.0 g) under ice-cooling, and the mixture was stirred from under ice-cooling to room temperature for 18 hr. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate. The solution was washed with aqueous citric acid solution and saturated brine, and filtrated through silica gel. The eluate was concentrated under reduced pressure, and the obtained pale-brown oil was crystallized from ethyl acetate-hexane to give the title compound (7.3 g, yield 88%) as pale-brown crystals. MS: 413 (MH+). melting point: 138-139° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07652133B2 |
| 出典データセット | uspto-grants-2010_01 |
| ORD ID | ord-1610d74c26854347b0a5242d28f25b99 |
| 出典メモ | uspto-grants-2010_01 |