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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36886Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/36886

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiethyl EtherHCID 3283—
Edukt4-Bromophenylhydrazine hydrochlorideHCID 12157—
Edukt1,1-Dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylateHCID 19936603—
LösungsmittelIsopropanolHCID 3776—
Produkt5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indoleHCID 990534257%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05418242
Quelldatensatzuspto-grants-1995_05
ORD IDord-2f1d1b5dffd3455f9f2cc1fcb715958f
Quellennotizuspto-grants-1995_05