7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

Base Information

Chemical Name:7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one
CAS No.:1465825-47-1
Molecular Formula:C₂₂H₁₇N₅O₄
Molecular Weight:415.408
Hs Code.:

Synonyms:7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

Suppliers and Price of 7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-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 7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

There total 5 articles about 7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-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:

: C₂₂H₁₉N₅O₄

: 1465825-47-1
7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; 1,4-dioxane; ethanol; Reflux;
DOI:10.1016/j.ejmech.2014.01.039

Reference yield:

: 88374-20-3
C₁₀H₁₀FN₃O₆

: 1465825-47-1
7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran

2: ammonium formate; palladium 10% on activated carbon / tetrahydrofuran; ethanol / 2 h / 20 °C

3: acetic acid / tetrahydrofuran; ethanol; 1,4-dioxane

4: 2,3-dicyano-5,6-dichloro-p-benzoquinone / tetrahydrofuran; ethanol; 1,4-dioxane / Reflux

With palladium 10% on activated carbon; ammonium formate; acetic acid; N-ethyl-N,N-diisopropylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1016/j.ejmech.2014.01.039

Reference yield:

: 1580534-27-5
C₁₈H₂₀N₄O₆

: 1465825-47-1
7-methyl-2-(5-nitrofuran-2-yl)-1-(phenylethyl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: ammonium formate; palladium 10% on activated carbon / tetrahydrofuran; ethanol / 2 h / 20 °C

2: acetic acid / tetrahydrofuran; ethanol; 1,4-dioxane

3: 2,3-dicyano-5,6-dichloro-p-benzoquinone / tetrahydrofuran; ethanol; 1,4-dioxane / Reflux

With palladium 10% on activated carbon; ammonium formate; acetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1016/j.ejmech.2014.01.039