ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

Base Information

Chemical Name:ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate
CAS No.:1401803-64-2
Molecular Formula:C₂₁H₂₁ClN₂O₄S
Molecular Weight:432.928
Hs Code.:

Synonyms:ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

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Chemical Property of ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

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Technology Process of ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

There total 1 articles about ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate 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: 71.0%

: 63-74-1
sulfanilamide

: 162758-34-1
ethyl [2-acetyl-4-(4-chlorophenyl)-3-methyl-4-oxo]butyrate

: 1401803-64-2
ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

Guidance literature:: With acetic acid; at 95 ℃; for 17h;

Reference yield: 98.0%

: 1401803-64-2
ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

: 1401803-66-4
5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate; With water; sodium hydroxide; In ethanol; for 3h; Reflux;

With hydrogenchloride; In water; pH=<= 7;

Reference yield:

: 1401803-64-2
ethyl 5-(4-chlorophenyl)-2,4-dimethyl-1-(4-sulfamoylphenyl)-1H-pyrrole-3-carboxylate

: C₂₂H₂₁Cl₂N₃O₃S

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide; water / ethanol / 3 h / Reflux

1.2: pH <= 7

2.1: oxalyl dichloride / dichloromethane / 1 h / 0 - 20 °C / Inert atmosphere

With oxalyl dichloride; water; sodium hydroxide; In ethanol; dichloromethane;