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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 523450Erstellt: 26. Oktober 2026

6(5H)-Phenanthridinone → 5-[3-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl]-5H-phenanthridin-6-one

https://huagongshe.com/reaction/523450

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6(5H)-PhenanthridinoneHCID 1853—
EduktPotassium CarbonateHCID 11430—
Edukt1,3-Di(2-pyridyl)-1,3-propanedioneHCID 2728494—
Edukt2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazineHCID 58943302—
KatalysatorCopper iodideHCID 83717—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-[3-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl]-5H-phenanthridin-6-oneHCID 86732665—

Reaktionsschritte

20 g (102 4 mmol) of 5H-phenanthridin-6-one, 43 g (112 mmol) of 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine, 2.3 g (10 2 mmol) of 1,3-bis[2-pyridyl]-1,3-propanedione, 28.3 g (204 mmol) of potassium carbonate and 1.9 g (10.2) of copper iodide are stirred under reflux in 1000 ml of DMF for 90 h. The solution is diluted with water and extracted twice with ethyl acetate, the combined organic phases are dried over Na2SO4, evaporated in a rotary evaporator and purified by chromatography (EtOAc/hexane: 2/3). The residue is recrystallised from toluene and from dichloromethane and finally sublimed in a high vacuum, purity is 99.9%. The yield is 31 g (62 mmol), corresponding to 61% of theory.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09337430B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-e7ed437354c74910853f4256e480fb4c
Quellennotizuspto-grants-2016_05