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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2195835Erstellt: 25. Oktober 2026

Triethylamine → chloro-2,3,4,5-tetrahydro-2-methyl-5-(2-morpholinoethyl)-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/2195835

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
Edukt4-(2-Bromoethyl)morpholineHCID 1502101—
Edukt1-Methylpiperidin-4-one hydrochlorideHCID 12210057—
LösungsmittelEthanolHCID 702—
Produktchloro-2,3,4,5-tetrahydro-2-methyl-5-(2-morpholinoethyl)-1H-pyrido[4,3-b]indoleHCID 86634532—

Reaktionsschritte

Preparation of the title compound was carried out according to General Method 8. 4-Chlorophenylhydrazine hydrochloride (2 g, 11 mmol), 4-(2-bromoethyl)morpholine (2.1 g, 11 mmol), triethyl amine (4.6 ml, 33 mmol) and N-methyl-4-piperidone hydrochloride (1.6 g, 11 mmol) were combined in ethanol (20 ml) to obtain 180 mg of -chloro-2,3,4,5-tetrahydro-2-methyl-5-(2-morpholinoethyl)-1H-pyrido[4,3-b]indole after purification on silica gel (230-400 mesh) chromatography eluting with acetone-hexane gradient. The free base was converted into its dioxalate salt by treatment of oxalic acid (2 equiv) in anhydrous THF.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08338408B2
Quelldatensatzuspto-grants-2012_12
ORD IDord-baa0c59f88dc4fd689236c749db5c3ee
Quellennotizuspto-grants-2012_12