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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1034427Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1034427

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 9905342—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05317025
Quelldatensatzuspto-grants-1994_05
ORD IDord-e510e489d86545898b603bf74b9401e4
Quellennotizuspto-grants-1994_05