Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36886Generated: October 25, 2026

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

https://huagongshe.com/reaction/36886

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 990534257%

Reaction Steps

4-Bromophenylhydrazine hydrochloride (11.5 g) is solubilized in a solution of 1,1-dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylate (14 g, prepared in Example 11) 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 numberUS05418242
Source datasetuspto-grants-1995_05
ORD IDord-2f1d1b5dffd3455f9f2cc1fcb715958f
Source noteuspto-grants-1995_05