ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

Base Information

Chemical Name:ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate
CAS No.:1609648-96-5
Molecular Formula:C₂₀H₂₀ClN₃O₄S
Molecular Weight:433.915
Hs Code.:

Synonyms:ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

Suppliers and Price of ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

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 ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

There total 5 articles about ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate 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: 93.0%

: 1609648-86-3
ethyl 4-(2-(tert-butyldimethylsilyl)-5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

: 1609648-96-5
ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

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

: 1609648-96-5
ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

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: 1 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:

: 1609648-55-6
ethyl 4-(2-(tert-butyldimethylsilyl)-1-(N,N-dimethylsulfamoyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)imidazol-4-yl)benzoate

: 1609648-96-5
ethyl 4-(5-(4-chlorophenyl)-1-(N,N-dimethylsulfamoyl)imidazol-4-yl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

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

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

1.3: 1 h / 50 °C / Inert atmosphere

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

With TurboGrignard; tetrabutyl ammonium fluoride; In tetrahydrofuran; water; 1.3: |Negishi Coupling;
DOI:10.1002/anie.201309217