2,3,4,9-Tetrahydro-4-methyl-1H-pyrido[3,4-b]indole → 4-Methyl-9H-beta-carboline

Reaktionsgleichung

[CH3:1][CH:2]1[C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[NH:7][C:6]=2[CH2:5][NH:4][CH2:3]1>[Pd]>[CH3:1][C:2]1[C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[NH:7][C:6]=2[CH:5]=[N:4][CH:3]=1

Komponenten

Reaktionsbedingungen

Temperatur: 160 °C

Versuchsvorschrift

4-methyl-2,3,4,9-tetrahydro-1H-β-carboline (214 mg, 1.17 mmol) was suspended in xylenes (10 ml). Pd (10% wt. on carbon, 21 mg) catalyst was added thereto and the reaction mixture was stirred at 160° C. for 24 hours, then cooled to RT and filtered through celite. The filtrate was concentrated to dryness to give 4-methyl-9H-β-carboline (210 mg).

Aufarbeitung

temperaturecooled to RT
filtrationfiltered through celite
concentrationThe filtrate was concentrated to dryness

Quellen und Nachweise

ORD-Eintrag: ord-5a8b7785a1c44cd4a637d2c07fb8374d
Quelldatensatz: uspto-grants-2010_06
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07727985B2

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Komponenten

Edukt 1

HCID 593375522,3,4,9-Tetrahydro-4-methyl-1H-pyrido[3,4-b]indole

Produkt 1

HCID 593375704-Methyl-9H-beta-carbolineAusbeute 98,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 23938PalladiumKatalysator