5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid

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Chemical Name:5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid
CAS No.:1384513-16-9
Molecular Formula:C₃₁H₃₁ClN₄O₄
Molecular Weight:559.065
Hs Code.:

Synonyms:5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid

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Chemical Property of 5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid

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Technology Process of 5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid

There total 5 articles about 5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-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: 73.0%

: 6269-89-2
1-(4-Nitrophenyl)piperazine

: 1384513-12-5
5-(4-chlorophenyl)-4-(3-iodophenyl)-1-isopropyl-2-methyl-1H-pyrrole-3-carboxylic acid

: 1384513-16-9
5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: With copper(l) iodide; potassium carbonate; L-proline; In dimethyl sulfoxide; at 80 ℃; Inert atmosphere;
DOI:10.1021/jm300608w

Reference yield:

: C₁₅H₁₇IO₃

: 1384513-16-9
5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide / 5 h / 70 °C

2: methanol / 24 h / Sealed tube

3: sulfuric acid / dichloromethane; tetrahydrofuran / 0.17 h / 0 °C

4: L-proline; copper(l) iodide / dimethyl sulfoxide / Inert atmosphere; Heating

With copper(l) iodide; sulfuric acid; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; triethylamine; L-proline; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; 1: |Stetter 1,4-Dicarbonyl Synthesis / 2: |Paal-Knorr Pyrrole Synthesis / 4: |Ullmann Condensation;
DOI:10.1021/jm4001105

Reference yield:

: 1428145-83-8
tert-butyl 2-acetyl-4-(4-chlorophenyl)-3-(3-iodophenyl)-4-oxobutanoate

: 1384513-16-9
5-(4-chlorophenyl)-1-isopropyl-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: methanol / 24 h / Sealed tube

2: sulfuric acid / dichloromethane; tetrahydrofuran / 0.17 h / 0 °C

3: L-proline; copper(l) iodide / dimethyl sulfoxide / Inert atmosphere; Heating

With copper(l) iodide; sulfuric acid; L-proline; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; 1: |Paal-Knorr Pyrrole Synthesis / 3: |Ullmann Condensation;
DOI:10.1021/jm4001105