N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

Base Information

Chemical Name:N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide
CAS No.:1383854-12-3
Molecular Formula:C₂₆H₂₉N₃O₆S₂
Molecular Weight:543.665
Hs Code.:

Synonyms:N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

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Chemical Property of N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

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Technology Process of N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

There total 4 articles about N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)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: 68.0%

: 1383854-11-2
N-(2-(4-(benzyloxy)phenyl)-5-cyclopropyl-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

: 1383854-12-3
N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

Guidance literature:: With hydrogen; 20% palladium hydroxide-activated charcoal; In N,N-dimethyl-formamide; for 32h; under 1551.49 Torr;

Reference yield:

: 20582-85-8
4-(methylthio)-1-butanol

: 1383854-12-3
N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: Oxone / methanol; water / 1.17 h / 0 - 20 °C

2: triethylamine / dichloromethane / 64 h / 0 - 20 °C

3: potassium carbonate / dimethyl sulfoxide / 24 h / 50 °C

4: hydrogen / 20% palladium hydroxide-activated charcoal / N,N-dimethyl-formamide / 32 h / 1551.49 Torr

With Oxone; hydrogen; potassium carbonate; triethylamine; 20% palladium hydroxide-activated charcoal; In methanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 26981-51-1
4-(Methylsulfonyl)-1-butanol

: 1383854-12-3
N-(5-cyclopropyl-2-(4-hydroxyphenyl)-3-(1H-imidazol-2-yl)benzofuran-6-yl)-N-(4-(methylsulfonyl)butyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 64 h / 0 - 20 °C

2: potassium carbonate / dimethyl sulfoxide / 24 h / 50 °C

3: hydrogen / 20% palladium hydroxide-activated charcoal / N,N-dimethyl-formamide / 32 h / 1551.49 Torr

With hydrogen; potassium carbonate; triethylamine; 20% palladium hydroxide-activated charcoal; In dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;