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HRID 637650作成日:2026年10月26日
3-(Dimethylamino)propyl chloride hydrochloride → 3-(3-[N,N-Dimethylamino]propylthio)-1-phenylindole hydrochloride
https://huagongshe.com/reaction/637650
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-(Dimethylamino)propyl chloride hydrochloride | HCID 94308 | — |
| 反応物 | 2-(1-Phenylindol-3-yl)-2-thioisourea hydroiodide | HCID 20255698 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Sodium Hydroxide | HCID 14798 | — |
| 生成物 | 3-(3-[N,N-Dimethylamino]propylthio)-1-phenylindole hydrochloride | HCID 20255707 | 46% |
反応手順
A suspension of the hydroidide salt from part (A) (27.0 g; 0.07M) in 2N aqueous sodium hydroxide (300.0 ml) was stirred under nitrogen and heated to reflux. After 10 minutes the mixture was cooled to 90° and solid 3-[dimethylamino]-propyl chloride hydrochloride (21.6 g; 0.14M) was added in small portions. A vigorous exothermic reaction occcurred and the solid dissolved. The solution was allowed to cool and was stirred at 20° for a further 17 hours. The resulting two-phase mixture was extracted with methylene chloride (3×100 ml.), and the combined organic extracts were washed with water (2×50 ml), dried (magnesium sulphate) and evaporated to give a viscous pale green oil. This was dissolved in 3.5N methanolic hydrogen chloride (50 ml.), evaporated and the residue was crystallised from acetonitrile (1200 ml.) to give the title compound as colourless leaflets, weight 11.3 g, m.p. 203°-7° (46.0% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04558048 |
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| 出典データセット | uspto-grants-1985_12 |
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| ORD ID | ord-6694d873829d4d669d5a5ba4bb56faa7 |
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| 出典メモ | uspto-grants-1985_12 |
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