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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523450생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/523450

반응식

참여 물질

역할이름HCID투입량
반응물6(5H)-PhenanthridinoneHCID 1853—
반응물Potassium CarbonateHCID 11430—
반응물1,3-Di(2-pyridyl)-1,3-propanedioneHCID 2728494—
반응물2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazineHCID 58943302—
촉매Copper iodideHCID 83717—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-[3-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl]-5H-phenanthridin-6-oneHCID 86732665—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09337430B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-e7ed437354c74910853f4256e480fb4c
출처 메모uspto-grants-2016_05