12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide

Base Information

Chemical Name:12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide
CAS No.:1392830-47-5
Molecular Formula:Br*C₃₀H₂₄N₃O₂
Molecular Weight:538.443
Hs Code.:

Synonyms:12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide

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Chemical Property of 12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide

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Technology Process of 12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide

There total 3 articles about 12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 1392830-45-3
12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one

: 1392830-47-5
12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide

Guidance literature:: With N-Bromosuccinimide; In ethyl acetate; at 20 ℃; for 3h; Darkness;
DOI:10.3998/ark.5550190.0013.624

Reference yield:

: 64369-54-6
7-(dimethylamino)-4-hydroxy-2H-1-benzopyran-2-one

: 1392830-47-5
12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide

Guidance literature:: Multi-step reaction with 4 steps

1.1: trichlorophosphate / 0.5 h / 0 - 50 °C

1.2: 12 h / 50 - 60 °C

2.1: triethylamine / ethanol / 4 h / Reflux

3.1: triethylamine / chloroform / 4 h / 20 °C

4.1: N-Bromosuccinimide / ethyl acetate / 3 h / 20 °C / Darkness

With N-Bromosuccinimide; triethylamine; trichlorophosphate; In ethanol; chloroform; ethyl acetate;
DOI:10.3998/ark.5550190.0013.624

Reference yield:

: 122978-34-1
4-chloro-7-dimethylamino-2-oxo-2H-1-benzopyran-3-carboxaldehyde

: 1392830-47-5
12-(dimethylamino)-15-oxo-1-phenyl-1,2,3,15-tetrahydrochromeno[3,4-j]imidazo[1,2-f]phenanthridin-4-ium bromide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / ethanol / 4 h / Reflux

2: triethylamine / chloroform / 4 h / 20 °C

3: N-Bromosuccinimide / ethyl acetate / 3 h / 20 °C / Darkness

With N-Bromosuccinimide; triethylamine; In ethanol; chloroform; ethyl acetate;
DOI:10.3998/ark.5550190.0013.624