3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid

Base Information

• Chemical Name: 3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid
• CAS No.: 1208317-17-2
• Molecular Formula: C₂₂H₂₂N₄O₄S₂
• Molecular Weight: 470.573
• Mol file: 1208317-17-2.mol

Synonyms:3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid

Chemical Property of 3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid

There total 6 articles about 3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic 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: 31.0%

3-(2-(3-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-3-oxopropyl)-1,3-dioxolan-2-yl)propanoic acid (1338799-46-4) + 4-amino-3-methylbenzenesulfonamide (53297-70-4) → 3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid (1208317-17-2)

Guidance literature:

In acetic acid; at 120 ℃;

DOI:10.1016/j.bmcl.2012.01.047

Reference yield:

4-acetamido-3-methylbenzenesulfonic acid → 3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid (1208317-17-2)

Guidance literature:

Multi-step reaction with 4 steps

1.1: sodium hydroxide / pyridine / 3 h / 20 °C

1.2: 2 h / -30 - 40 °C

2.1: ammonium hydroxide / tetrahydrofuran / 1 h / 0 - 20 °C

3.1: hydrogenchloride / ethanol; water / 80 °C

4.1: acetic acid / 120 °C

With hydrogenchloride; ammonium hydroxide; sodium hydroxide; In tetrahydrofuran; pyridine; ethanol; water; acetic acid;

DOI:10.1016/j.bmcl.2012.01.047

Reference yield:

2-aminotoluene-5-sulfonic acid (98-33-9) → 3-(5-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-1-(2-methyl-4-sulfamoylphenyl)-1H-pyrrol-2-yl)propanoic acid (1208317-17-2)

Guidance literature:

Multi-step reaction with 5 steps

1.1: pyridine / 2 h / 20 °C

2.1: sodium hydroxide / pyridine / 3 h / 20 °C

2.2: 2 h / -30 - 40 °C

3.1: ammonium hydroxide / tetrahydrofuran / 1 h / 0 - 20 °C

4.1: hydrogenchloride / ethanol; water / 80 °C

5.1: acetic acid / 120 °C

With pyridine; hydrogenchloride; ammonium hydroxide; sodium hydroxide; In tetrahydrofuran; pyridine; ethanol; water; acetic acid;

DOI:10.1016/j.bmcl.2012.01.047

upstream raw materials:

3-(2-(3-(5-(2-methyl-1H-imidazol-1-yl)thiophen-2-yl)-3-oxopropyl)-1,3-dioxolan-2-yl)propanoic acid

4-amino-3-methylbenzenesulfonamide

2-aminotoluene-5-sulfonic acid

N-[4-(aminosulfonyl)-2-methylphenyl]acetamide