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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64543Erstellt: 24. Oktober 2026

1,4-Diaminocyclohexane → 2-bromo-9-(pyridin-2-yl)-9H-carbazole

https://huagongshe.com/de/reaction/64543

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DiaminocyclohexaneHCID 18374—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2-IodopyridineHCID 221126—
Edukt2-Bromo-9H-carbazoleHCID 12717089—
KatalysatorCopper iodideHCID 83717—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-bromo-9-(pyridin-2-yl)-9H-carbazoleHCID 7065485243,2%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

A 100 mL 3-neck flask was charged with copper iodide (0.057 g, 0.301 mmol), 2-bromo-9H-carbazole (7.4 g, 30.1 mmol), 2-iodopyridine (12.3 g, 60.1 mmol), potassium phosphate (12.8 g, 60.1 mmol), (1R,4R)-cyclohexane-1,4-diamine (0.343 g, 3.0 mmol), and dioxane (25 mL) and the reaction mixture was heated at 65° C. for 16 hours. The reaction mixture was then poured into deionized water and extracted with dichloromethane The organic layers were combined and subjected to a column chromatography (neutral Al2O3, 99/1 hexane/EtOAc) to yield 4.2 g (43%) of 2-bromo-9-(pyridin-2-yl)-9H-carbazole as a white solid. The product was confirmed by GC/MS and NMR.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09450195B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-025f65fadd3e46f68e5821f6da41c4a5
Quellennotizuspto-grants-2016_09