1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide

Base Information

• Chemical Name: 1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide
• CAS No.: 1277098-50-6
• Molecular Formula: C₁₉H₁₆N₄OS
• Molecular Weight: 348.428
• Mol file: 1277098-50-6.mol

Synonyms:1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide

Chemical Property of 1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide

There total 4 articles about 1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide 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: 97.0%

1-benzyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxylic acid (1277098-48-2) + methylamine (74-89-5) → 1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide (1277098-50-6)

Guidance literature:

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃;

DOI:10.1002/ardp.201000167

Reference yield:

methyl 1-benzyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxylate (1277098-46-0) → 1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide (1277098-50-6)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride; water / 5 h / 60 °C

2: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With hydrogenchloride; dmap; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane;

DOI:10.1002/ardp.201000167

Reference yield:

3-amino-4-benzylamine-benzoic acid methyl ester (68502-22-7) → 1-benzyl-N-methyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxamide (1277098-50-6)

Guidance literature:

Multi-step reaction with 4 steps

1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

2: acetic acid / 5 h / Reflux

3: hydrogenchloride; water / 5 h / 60 °C

4: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With hydrogenchloride; dmap; water; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane;

DOI:10.1002/ardp.201000167

upstream raw materials:

1-benzyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxylic acid

methylamine

methyl 1-benzyl-2-(thiazol-4-yl)-1H-benzoimidazole-5-carboxylate

3-amino-4-benzylamine-benzoic acid methyl ester