1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid

Base Information

Chemical Name:1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid
CAS No.:1561964-51-9
Molecular Formula:C₂₄H₃₁F₃N₂O₄S
Molecular Weight:500.582
Hs Code.:

Synonyms:1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid

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Chemical Property of 1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid

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Technology Process of 1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid

There total 7 articles about 1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid 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%

: 1561964-48-4
ethyl 1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylate

: 1561964-51-9
1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid

Guidance literature:: With potassium tert-butylate; water; In dimethyl sulfoxide; at 90 ℃; for 1h;

Reference yield:

: 6339-66-8
ethyl 5-formyl-4-methyl-1H-pyrrole-3-carboxylate

: 1561964-51-9
1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 - 20 °C

1.2: 30 °C

2.1: tetrahydrofuran / 0 - 25 °C

3.1: trifluoroacetic acid / dichloromethane / 0.25 h / 0 °C

3.2: 0 - 20 °C

4.1: ammonium cerium (IV) nitrate / water; acetonitrile / 0.67 h / 20 °C

5.1: potassium phosphate; trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide / toluene / Inert atmosphere; Reflux

6.1: potassium tert-butylate; water / dimethyl sulfoxide / 1 h / 90 °C

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; potassium phosphate; copper(l) iodide; ammonium cerium (IV) nitrate; potassium tert-butylate; water; sodium hydride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; toluene; acetonitrile; mineral oil;

Reference yield:

: 1561964-36-0
ethyl 5-formyl-1-(4-methoxybenzyl)-4-methyl-1H-pyrrole-3-carboxylate

: 1561964-51-9
1-(4-(N-(tert-butyl)sulfamoyl)-3-(trifluoromethyl)phenyl)-5-(cyclohexylmethyl)-4-methyl-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: tetrahydrofuran / 0 - 25 °C

2.1: trifluoroacetic acid / dichloromethane / 0.25 h / 0 °C

2.2: 0 - 20 °C

3.1: ammonium cerium (IV) nitrate / water; acetonitrile / 0.67 h / 20 °C

4.1: potassium phosphate; trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide / toluene / Inert atmosphere; Reflux

5.1: potassium tert-butylate; water / dimethyl sulfoxide / 1 h / 90 °C

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; potassium phosphate; copper(l) iodide; ammonium cerium (IV) nitrate; potassium tert-butylate; water; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; toluene; acetonitrile;