関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1,2,3,4-Tetrahydroquinoline | HCID 69460 | — |
| 反応物 | 3,4-Dimethoxybenzenesulfonyl chloride | HCID 2734183 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(3,4-Dimethoxybenzenesulphonyl)-1,2,3,4-tetrahydroquinoline | HCID 667562 | — |
反応手順
1,2,3,4-Tetrahydroquinoline (0.29 ml) was added to a suspension of 3,4-dimethoxybenzene sulphonyl chloride (0.50 g) in dichloromethane (15 ml) at room temperature. Triethylamine (0.44 ml) was added and the resulting mixture stirred for 24 hours at room temperature. The reaction mixture was then diluted with dichloromethane (20 ml) and washed successively with saturated aqueous sodium hydrogen carbonate solution (10 ml), 2N hydrochloric acid (10 ml) and saturated aqueous sodium chloride solution (10 ml). Drying over magnesium sulphate and concentration in vacuo provided a yellow oil. Purification by column chromatography eluting with 30% ethyl acetate in hexane provided the title compound as a colourless oil (0.60 g) which solidified on standing.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05728712 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-80b4d3c6a338477cbce6e4a97e49acd8 |
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| 出典メモ | uspto-grants-1998_03 |
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