N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide

Base Information

Chemical Name:N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide
CAS No.:1283118-22-8
Molecular Formula:C₂₅H₂₄N₄O₇S
Molecular Weight:524.554
Hs Code.:

Synonyms:N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide

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Chemical Property of N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide

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Technology Process of N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide

There total 6 articles about N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide 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: 68.9%

: 1283118-23-9
2-ethoxy-4-(6-(4-(methylsulfonamido)phenyl)-2-oxo-5-phenyl-1,2,3,4-tetrahydropyrimidin-4-yl)-6-nitrophenyl methanesulfonate

: 1283118-22-8
N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide

Guidance literature:: 2-ethoxy-4-(6-(4-(methylsulfonamido)phenyl)-2-oxo-5-phenyl-1,2,3,4-tetrahydropyrimidin-4-yl)-6-nitrophenyl methanesulfonate; With water; sodium hydroxide; In ethanol; at 0 - 80 ℃; for 5h;

With hydrogenchloride; In ethanol; water; at 20 ℃; pH=5;

Reference yield:

: 2001-29-8
1-(4-bromophenyl)-2-phenyl-ethan-1-one

: 1283118-22-8
N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / ethanol; water / Reflux

2.1: caesium carbonate / bis(dibenzylideneacetone)-palladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / Inert atmosphere; Reflux

3.1: hydrogenchloride; water / tetrahydrofuran / 2 h / 20 °C

4.1: triethylamine / dichloromethane / 5 h / 0 °C

5.1: sodium hydroxide; water / ethanol / 5 h / 0 - 80 °C

5.2: 20 °C / pH 5

With hydrogenchloride; water; caesium carbonate; triethylamine; sodium hydroxide; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water;

Reference yield:

: 178686-24-3
3-ethoxy-4-hydroxy-5-nitrobenzaldehyde

: 1283118-22-8
N-(4-(6-(3-ethoxy-4-hydroxy-5-nitrophenyl)-2-oxo-5-phenyl-1,2,3,6-tetrahydropyrimidin-4-yl)phenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / ethanol; water / Reflux

2.1: caesium carbonate / bis(dibenzylideneacetone)-palladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / Inert atmosphere; Reflux

3.1: hydrogenchloride; water / tetrahydrofuran / 2 h / 20 °C

4.1: triethylamine / dichloromethane / 5 h / 0 °C

5.1: sodium hydroxide; water / ethanol / 5 h / 0 - 80 °C

5.2: 20 °C / pH 5

With hydrogenchloride; water; caesium carbonate; triethylamine; sodium hydroxide; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; bis(dibenzylideneacetone)-palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water;