4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide

Base Information

Chemical Name:4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide
CAS No.:1179329-08-8
Molecular Formula:C₂₇H₂₃F₃N₆O₅S
Molecular Weight:600.578
Hs Code.:

Synonyms:4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide

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Chemical Property of 4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide

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Technology Process of 4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide

There total 8 articles about 4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide 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:

: 1179329-74-8
4-(3-{2-[3-(4-cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonyl chloride

: 1179329-08-8
4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide

Guidance literature:: With ammonia; In methanol; at 20 ℃; for 72h;

Reference yield:

: 654-70-6
4-amino-2-trifluoromethylbenzonitrile

: 1179329-08-8
4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: toluene; acetonitrile / 70 °C

1.2: 20 °C

1.3: 1 h / 70 °C

2.1: potassium carbonate / acetonitrile / 5 h / 20 °C

3.1: caesium carbonate; Benzophenone imine / palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 6 h / 95 °C / Inert atmosphere

3.2: 0.17 h / 20 °C

4.1: tetrahydrofuran / 20 °C

5.1: ammonia / methanol / 72 h / 20 °C

With Benzophenone imine; ammonia; potassium carbonate; caesium carbonate; palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; methanol; toluene; acetonitrile;

Reference yield:

: 143782-20-1
4-(4,4-dimethyl-2,5-dioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

: 1179329-08-8
4-(3-{2-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-ylmethyl]phenyl}ureido)benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetonitrile / 5 h / 20 °C

2.1: caesium carbonate; Benzophenone imine / palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 6 h / 95 °C / Inert atmosphere

2.2: 0.17 h / 20 °C

3.1: tetrahydrofuran / 20 °C

4.1: ammonia / methanol / 72 h / 20 °C

With Benzophenone imine; ammonia; potassium carbonate; caesium carbonate; palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; methanol; acetonitrile;