Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 509688Erstellt: 25. Oktober 2026

Phenethyl bromide → 8-chloro-2,3,4,5-tetrahydro-2-methyl-5-phenethyl-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/509688

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethyl bromideHCID 7666—
EduktTriethylamineHCID 8471—
EduktHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
EduktTrifluoroacetateHCID 84468—
Edukt1-Methylpiperidin-4-one hydrochlorideHCID 12210057—
LösungsmittelEthanolHCID 702—
Produkt8-chloro-2,3,4,5-tetrahydro-2-methyl-5-phenethyl-1H-pyrido[4,3-b]indoleHCID 578759361,7%

Reaktionsschritte

Preparation of the title compound was carried out according to General Method 8. 4-Chlorophenylhydrazine hydrochloride (500 mg, 2.79 mmol), 2-phenyl ethyl bromide (0.38 ml, 2.79 mmol), triethyl amine (0.39 ml, 2.79 mmol) and N-methyl-4-piperidone hydrochloride (623 mg, 4.18 mmol) were combined in ethanol (2 ml) to obtain 15 mg of 8-chloro-2,3,4,5-tetrahydro-2-methyl-5-phenethyl-1H-pyrido[4,3-b]indole as a trifluoroacetate salt after purification on neutral alumina using ethyl acetate-hexane gradient followed by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096591B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-5eee7a1f408b4bffaa50173b7dc3b272
Quellennotizuspto-grants-2015_08