ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate

Base Information

• Chemical Name: ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate
• CAS No.: 852854-23-0
• Molecular Formula: C₁₄H₁₅ClN₄O₂S
• Molecular Weight: 338.818
• Mol file: 852854-23-0.mol

Synonyms:ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate

Chemical Property of ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate

There total 3 articles about ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-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: 75.0%

4-Chlorophenyl isothiocyanate (2131-55-7) + 5-amino-1-methyl-1H-imidazole-4-carboxylic acid ethyl ester (54147-04-5) → ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate (852854-23-0)

Guidance literature:

In pyridine; at 45 ℃; for 17h;

Reference yield:

C8H16N2O3 → ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate (852854-23-0)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol; acetonitrile / 18 h / 20 °C

2: pyridine / 18 h / 45 °C

With pyridine; In ethanol; acetonitrile;

Reference yield:

ethyl 2,3-diamino propionate (72809-03-1,150408-87-0) → ethyl 5-({[(4-chlorophenyl)amino]carbonothioyl}amino)-1-methyl-1H-imidazole-4-carboxylate (852854-23-0)

Guidance literature:

Multi-step reaction with 3 steps

1: acetonitrile / 1 - 1.17 h / 90 °C

2: ethanol; acetonitrile / 18 h / 20 °C

3: pyridine / 18 h / 45 °C

With pyridine; In ethanol; acetonitrile;

upstream raw materials:

4-Chlorophenyl isothiocyanate

5-amino-1-methyl-1H-imidazole-4-carboxylic acid ethyl ester

ethyl 2,3-diamino propionate

Downstream raw materials:

1-(4-chlorophenyl)-9-methyl-2-thioxo-1,2,3,9-tetrahydro-6H-purin-6-one hydrochloride