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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034427Generated: October 26, 2026

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

https://huagongshe.com/reaction/1034427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant4-Bromophenylhydrazine hydrochlorideHCID 12157—
Reactant1,1-Dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylateHCID 19936603—
SolventIsopropanolHCID 3776—
Product5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indoleHCID 9905342—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317025
Source datasetuspto-grants-1994_05
ORD IDord-e510e489d86545898b603bf74b9401e4
Source noteuspto-grants-1994_05