2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Base Information

Chemical Name:2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester
CAS No.:908371-35-7
Molecular Formula:C₂₉H₂₄N₄O₄
Molecular Weight:492.534
Hs Code.:

2-amino-3-{[2-(2-benzyloxy-phenyl)-1<i>H</i>-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Synonyms:2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Suppliers and Price of 2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

There total 14 articles about 2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester 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:

: 95067-27-9
2-acetylamino-3-nitro-benzoic acid methyl ester

: 908371-35-7
2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: sodium methoxide / methanol / 20 °C

2: 96 percent / hydrogen / Pd/C / methanol / 3 h

3: 0.27 g / triethylamine / CH₂Cl₂ / 20 °C

With hydrogen; sodium methylate; triethylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1016/j.bmc.2006.05.007

Reference yield:

: 2719-08-6
methyl 2-(acetylamino)benzoate

: 908371-35-7
2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: acetic anhydride; acetic acid; nitric acid / 2.5 h / 5 - 15 °C

2: sodium methoxide / methanol / 20 °C

3: 96 percent / hydrogen / Pd/C / methanol / 3 h

4: 0.27 g / triethylamine / CH₂Cl₂ / 20 °C

With hydrogen; nitric acid; sodium methylate; acetic anhydride; acetic acid; triethylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1016/j.bmc.2006.05.007

Reference yield:

: 606-18-8
3-nitroanthranilic acid

: 908371-35-7
2-amino-3-{[2-(2-benzyloxy-phenyl)-1H-benzoimidazole-4-carbonyl]-amino}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: diethyl ether / 0 °C

2: 96 percent / hydrogen / Pd/C / methanol / 3 h

3: 0.27 g / triethylamine / CH₂Cl₂ / 20 °C

With hydrogen; triethylamine; palladium on activated charcoal; In methanol; diethyl ether; dichloromethane;
DOI:10.1016/j.bmc.2006.05.007