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Hydrochloric Acid → 5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| 反応物 | 1,1-Dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylate | HCID 19936603 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indole | HCID 9905342 | — |
反応手順
4-Bromophenylhydrazine hydrochloride (11.5 g) is solubilized in a solution of 1,1-dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylate (prepared in Example 10) in isopropanol (100 ml) under nitrogen. The solution is cooled to 0° C. and saturated with gaseous hydrogen chloride. After 4 hours at room temperature, the precipitate is filtered off, taken up in sodium hydroxide and extracted with ether and then with methylene chloride. The organic phases are combined, dried over sodium sulfate and concentrated. The solid obtained is taken up in the minimum amount of ether and recrystallized from xylene to give 5-bromo-2-methyl-3-(piperidin-4-ylthio) -1H-indole (9.5 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05317025 |
| 出典データセット | uspto-grants-1994_05 |
| ORD ID | ord-e510e489d86545898b603bf74b9401e4 |
| 出典メモ | uspto-grants-1994_05 |