4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

Base Information

Chemical Name:4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide
CAS No.:1609649-00-4
Molecular Formula:C₁₈H₁₅ClF₃N₃O₂S
Molecular Weight:429.85
Hs Code.:

Synonyms:4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

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Chemical Property of 4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

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Technology Process of 4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

There total 5 articles about 4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide 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: 100.0%

: 1609648-94-3
2-(tert-butyldimethylsilyl)-4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

: 1609649-00-4
4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; water; at 0 ℃; for 0.0833333h; Inert atmosphere; Schlenk technique;
DOI:10.1002/anie.201309217

Reference yield:

: 1609648-50-1
2-(tert-butyldimethylsilyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)N,N-dimethylimidazole-1-sulfonamide

: 1609649-00-4
4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex / tetrahydrofuran / 1 h / -30 °C / Inert atmosphere; Schlenk technique

1.2: 0.25 h / -30 °C / Inert atmosphere

1.3: 2 h / 50 °C / Inert atmosphere

2.1: TurboGrignard / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere; Schlenk technique

2.2: 0.25 h / -30 °C / Inert atmosphere

2.3: 2 h / 50 °C / Inert atmosphere

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran; water / 0.08 h / 0 °C / Inert atmosphere; Schlenk technique

With TurboGrignard; 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex; tetrabutyl ammonium fluoride; In tetrahydrofuran; water; 1.3: |Negishi Coupling / 2.3: |Negishi Coupling;
DOI:10.1002/anie.201309217

Reference yield:

: 78162-58-0
N,N-dimethyl-1H-imidazole-1-sulfonamide

: 1609649-00-4
4-(4-chlorophenyl)-N,N-dimethyl-5-(4-(trifluoromethyl)phenyl)imidazole-1-sulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: n-butyllithium / tetrahydrofuran / 0.25 h / -78 °C / Inert atmosphere

1.2: 1 h / -78 - 25 °C / Inert atmosphere

2.1: 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere; Schlenk technique

2.2: 4 h / -20 - 20 °C / Inert atmosphere; Schlenk technique

3.1: 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex / tetrahydrofuran / 1 h / -30 °C / Inert atmosphere; Schlenk technique

3.2: 0.25 h / -30 °C / Inert atmosphere

3.3: 2 h / 50 °C / Inert atmosphere

4.1: TurboGrignard / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere; Schlenk technique

4.2: 0.25 h / -30 °C / Inert atmosphere

4.3: 2 h / 50 °C / Inert atmosphere

5.1: tetrabutyl ammonium fluoride / tetrahydrofuran; water / 0.08 h / 0 °C / Inert atmosphere; Schlenk technique

With TurboGrignard; n-butyllithium; 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex; tetrabutyl ammonium fluoride; In tetrahydrofuran; water; 3.3: |Negishi Coupling / 4.3: |Negishi Coupling;
DOI:10.1002/anie.201309217