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Hydrogen Sulfide → 3-[2-(Dimethylamino)ethyl]-1H-indole-5-carbothioamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Sulfide | HCID 402 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Indole-5-carbonitrile, 3-(2-dimethylaminoethyl)- | HCID 28511 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-[2-(Dimethylamino)ethyl]-1H-indole-5-carbothioamide | HCID 20041356 | — |
反応手順
A solution of 3-[2-(dimethylamino)ethyl]-1H-indole-5-carbonitrile (13.0 g) and triethylamine (50 ml) in dimethylformamide (300 ml) was stirred for 2 h whilst gaseous hydrogen sulphide was bubbled through it. More triethylamine (10 ml) was added and the solution was stirred at room temperature for 2 days, then evaporated in vacuo to give an oil (15 g) which was partitioned between ethyl acetate (500 ml) and water (3×250 ml). The organic layer was dried (MgSO4) pre-absorbed onto silica and purified by flash chromatography (A). The appropriate fractions were combined, concentrated in vacuo and triturated with ether (250 ml) to give the title compound (12.0 g) as a solid, m.p. 155°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04833153 |
| 出典データセット | uspto-grants-1989_05 |
| ORD ID | ord-2faf13d4fbc9489b9d679b30d03af470 |
| 出典メモ | uspto-grants-1989_05 |