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HRID 2383272Erstellt: 26. Oktober 2026

2-methyl-6-nitro-2,3,4,9-tetrahydro-1H-beta-carboline → 2-methyl-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-amine

https://huagongshe.com/reaction/2383272

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-methyl-6-nitro-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 59843441—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt2-methyl-1H,2H,3H,4H,9H-pyrido[3,4-b]indol-6-amineHCID 59843438107%

Reaktionsschritte

To a solution of 2-methyl-6-nitro-2,3,4,9-tetrahydro-1H-β-carboline (description 1) (1.42 g, 6.13 mmol) in EtOH (300 mL), 570 mg of (5%) Pd/C were added. The mixture was hydrogenated under 20 psi at room temperature for 20 h and filtered through a pad of Celite. The EtOH was evaporated to dryness to yield 1.32 g of 6-amino-2-methyl-2,3,4,9-tetrahydro-1H-β-carboline that were used directly to synthesize compounds of formula I.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08263609B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-22b91244e89a41949e5896ad7360e274
Quellennotizuspto-grants-2012_09