1H-Benzimidazole-5-carboxamide, 2-(4-aminophenyl)-N-phenyl-

Base Information

Chemical Name:1H-Benzimidazole-5-carboxamide, 2-(4-aminophenyl)-N-phenyl-
CAS No.:820242-67-9
Molecular Formula:C20H16N4O
Molecular Weight:328.373
Hs Code.:
DSSTox Substance ID:DTXSID60465959
Wikidata:Q82292286

Synonyms:820242-67-9;1H-Benzimidazole-5-carboxamide, 2-(4-aminophenyl)-N-phenyl-;SCHEMBL19994477;SCHEMBL23830419;DTXSID60465959

Suppliers and Price of 1H-Benzimidazole-5-carboxamide, 2-(4-aminophenyl)-N-phenyl-

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 1 raw suppliers

Chemical Property of 1H-Benzimidazole-5-carboxamide, 2-(4-aminophenyl)-N-phenyl-

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:328.13241115
Heavy Atom Count:25
Complexity:457

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=O)C2=CC3=C(C=C2)N=C(N3)C4=CC=C(C=C4)N

Technology Process of 1H-Benzimidazole-5-carboxamide, 2-(4-aminophenyl)-N-phenyl-

There total 4 articles about 1H-Benzimidazole-5-carboxamide, 2-(4-aminophenyl)-N-phenyl- 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:

: 820242-65-7
2-(4-nitro-phenyl)-1H-benzoimidazole-5-carboxylic acid phenylamide

: 820242-67-9
2-(4-amino-phenyl)-1H-benzoimidazole-5-carboxylic acid phenylamide

Guidance literature:: With N,N-dimethyl-formamide; palladium on activated charcoal; In methanol;
DOI:10.1021/jm049288j

Reference yield:

: 555-16-8
4-nitrobenzaldehdye

: 820242-67-9
2-(4-amino-phenyl)-1H-benzoimidazole-5-carboxylic acid phenylamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: 55 percent / nitrobenzene / 18 h / 155 - 160 °C

2.1: 1,1'-carbonyldiimidazole / dimethylformamide / 3 h / 80 °C

2.2: dimethylformamide / 18 h / Heating

3.1: H₂ / Pd/C / ethanol; dimethylformamide / 6 h / 70 - 90 °C

With hydrogen; 1,1'-carbonyldiimidazole; palladium on activated charcoal; In ethanol; nitrobenzene; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2006.03.014

Reference yield:

: 69570-99-6
2-(4-nitrophenyl)-1H-benzimidazole-5-carboxylic acid

: 820242-67-9
2-(4-amino-phenyl)-1H-benzoimidazole-5-carboxylic acid phenylamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1,1'-carbonyldiimidazole / dimethylformamide / 3 h / 80 °C

1.2: dimethylformamide / 18 h / Heating

2.1: H₂ / Pd/C / ethanol; dimethylformamide / 6 h / 70 - 90 °C

With hydrogen; 1,1'-carbonyldiimidazole; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2006.03.014