戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 523450作成日:2026年10月27日

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

https://huagongshe.com/reaction/523450

反応式

関与物質

役割名称HCID仕込み量
反応物6(5H)-PhenanthridinoneHCID 1853—
反応物Potassium CarbonateHCID 11430—
反応物1,3-Di(2-pyridyl)-1,3-propanedioneHCID 2728494—
反応物2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazineHCID 58943302—
触媒Copper iodideHCID 83717—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-[3-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl]-5H-phenanthridin-6-oneHCID 86732665—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09337430B2
出典データセットuspto-grants-2016_05
ORD IDord-e7ed437354c74910853f4256e480fb4c
出典メモuspto-grants-2016_05