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HRID 1034427作成日:2026年10月26日

Hydrochloric Acid → 5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indole

https://huagongshe.com/reaction/1034427

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Diethyl EtherHCID 3283—
反応物4-Bromophenylhydrazine hydrochlorideHCID 12157—
反応物1,1-Dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylateHCID 19936603—
溶媒IsopropanolHCID 3776—
生成物5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05317025
出典データセットuspto-grants-1994_05
ORD IDord-e510e489d86545898b603bf74b9401e4
出典メモuspto-grants-1994_05