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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 710731Erstellt: 25. Oktober 2026

Diethylamine → 5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/710731

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethylamineHCID 8021—
EduktTrifluoroacetateHCID 84468—
Edukt2-Fluorophenethyl bromideHCID 2756964—
Edukt4-Iodophenylhydrazine hydrochlorideHCID 12208795—
Edukt1-Methylpiperidin-4-one hydrochlorideHCID 12210057—
LösungsmittelEthanolHCID 702—
Produkt5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indoleHCID 578762460,5%

Reaktionsschritte

Preparation of the title compound was carried out according to General Method 8. 4-Iodophenylhydrazine hydrochloride (500 mg, 2.1 mmol), 2-fluorophenethylbromide (0.3 ml, 2.1 mmol), diethyl amine (0.8 ml, 6.3 mmol) and N-methyl-4-piperidone hydrochloride (312 mg, 2.1 mmol) were taken in ethanol (10 ml) to obtain 5 mg of 5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indole as a trifluoroacetate salt after purification 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
PatentnummerUS09181240B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-9bbcfa681bea4946a7eb07358ad844df
Quellennotizuspto-grants-2015_11