4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid

Base Information

Chemical Name:4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid
CAS No.:1261266-13-0
Molecular Formula:C₃₃H₃₁N₃O₃
Molecular Weight:517.627
Hs Code.:

Synonyms:4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid

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Chemical Property of 4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid

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Technology Process of 4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid

There total 6 articles about 4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic 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: 71.2%

: 1261265-94-4
methyl 4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]biphenyl-2-carboxylate

: 1261266-13-0
4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid

Guidance literature:: methyl 4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]biphenyl-2-carboxylate; With methanol; sodium hydroxide; for 3h; Reflux;

With hydrogenchloride; In water; pH=6;
DOI:10.1016/j.ejmech.2012.01.009

Reference yield:

: 152628-03-0
4-methyl-2-n-propyl-1H-benzimidazole-6-carboxylic acid

: 1261266-13-0
4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: thionyl chloride / 4 h / Reflux

2.1: triethylamine / dichloromethane / 6 h / 20 °C / Cooling with ice

3.1: potassium tert-butylate / N,N-dimethyl-formamide / 0.5 h / Cooling with ice

3.2: Cooling with ice

4.1: methanol; sodium hydroxide / 3 h / Reflux

4.2: pH 6

With methanol; thionyl chloride; potassium tert-butylate; triethylamine; sodium hydroxide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.01.009

Reference yield:

: 4-methyl-2-n-propyl-1H-benzimidazole-6-carboxylic chloride

: 1261266-13-0
4'-[(6-benzylaminocarbonyl-4-methyl-2-propyl-1H-benzimidazolyl)methyl]-2-biphenylcarboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 6 h / 20 °C / Cooling with ice

2.1: potassium tert-butylate / N,N-dimethyl-formamide / 0.5 h / Cooling with ice

2.2: Cooling with ice

3.1: methanol; sodium hydroxide / 3 h / Reflux

3.2: pH 6

With methanol; potassium tert-butylate; triethylamine; sodium hydroxide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.01.009