3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

Base Information

Chemical Name:3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide
CAS No.:1542265-57-5
Molecular Formula:C₁₉H₁₅F₃IN₃O
Molecular Weight:485.247
Hs Code.:

Synonyms:3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

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Chemical Property of 3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

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Technology Process of 3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

There total 3 articles about 3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide 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: 72.2%

: 641570-89-0
4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)aniline

: 82998-57-0
3-iodo-4-toluic acid

: 1542265-57-5
3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

Guidance literature:: 3-iodo-4-toluic acid; With thionyl chloride; for 3h; Reflux;

4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)aniline; With dmap; triethylamine; In tetrahydrofuran; at 20 ℃; for 4h;

Reference yield:

: 910654-28-3
4-methyl-1-(2-(trifluoromethyl)-4-nitrophenyl)-1H-imidazole

: 1542265-57-5
3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen; palladium 10% on activated carbon / ethanol / 3 h / 2068.65 Torr

2.1: thionyl chloride / 3 h / Reflux

2.2: 4 h / 20 °C

With thionyl chloride; palladium 10% on activated carbon; hydrogen; In ethanol;

Reference yield:

: 400-74-8
2-Fluoro-5-nitrobenzotrifluoride

: 1542265-57-5
3-iodo-4-methyl-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / acetonitrile / 6 h / Reflux

2.1: hydrogen; palladium 10% on activated carbon / ethanol / 3 h / 2068.65 Torr

3.1: thionyl chloride / 3 h / Reflux

3.2: 4 h / 20 °C

With thionyl chloride; palladium 10% on activated carbon; hydrogen; potassium carbonate; In ethanol; acetonitrile;