1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

Base Information

Chemical Name:1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one
CAS No.:1465825-48-2
Molecular Formula:C₂₆H₂₅N₅O₆
Molecular Weight:503.514
Hs Code.:

Synonyms:1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

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Chemical Property of 1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

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Technology Process of 1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-1H-imidazo[4,5-g]quinoxalin-6(5H)-one

There total 6 articles about 1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-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:

: C₂₆H₂₇N₅O₆

: 1465825-48-2
1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-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:

: 137816-80-9
C₁₂H₁₄FN₃O₆

: 1465825-48-2
1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-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:

: 1580534-28-6
C₂₂H₂₈N₄O₈

: 1465825-48-2
1-(3,4-dimethoxyphenylethyl)-7-isopropyl-2-(5-nitrofuran-2-yl)-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