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

Base Information

Chemical Name:12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one
CAS No.:1392830-45-3
Molecular Formula:C₃₀H₂₅N₃O₂
Molecular Weight:459.547
Hs Code.:

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

Suppliers and Price of 12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

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

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

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

: Br^(1-)*C₂₄H₂₀BrN₂O₂⁽¹⁺⁾

: 62-53-3
aniline

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

Guidance literature:: With triethylamine; In chloroform; at 20 ℃; for 4h;
DOI:10.3998/ark.5550190.0013.624

Reference yield:

: 1-(2-bromo-ethyl)-4-methyl-quinolinium bromide

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

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / ethanol / 4 h / Reflux

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

With triethylamine; In ethanol; chloroform;
DOI:10.3998/ark.5550190.0013.624

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 3 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

With triethylamine; trichlorophosphate; In ethanol; chloroform;
DOI:10.3998/ark.5550190.0013.624