1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid

Base Information

Chemical Name:1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid
CAS No.:1372540-75-4
Molecular Formula:C₂₁H₂₀ClF₂N₃O₃
Molecular Weight:435.858
Hs Code.:

Synonyms:1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid

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Chemical Property of 1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid

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Technology Process of 1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid

There total 7 articles about 1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic 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: 80.0%

: C₂₂H₂₂ClF₂N₃O₃

: 1372540-75-4
1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid

Guidance literature:: C₂₂H₂₂ClF₂N₃O₃; With lithium hydroxide; In tetrahydrofuran; at 45 ℃; for 4h;

With formic acid; In water; pH=3;

Reference yield:

: 193481-78-6
3-Amino-5-chloro-2-nitrobenzoic acid

: 1372540-75-4
1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine; HATU / tetrahydrofuran / 3 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 110 °C

3.1: hydrogen / palladium on activated charcoal / methanol / 3 h / 20 °C / 3040.2 Torr / autoclave

4.1: toluene / 15 h / Reflux

5.1: potassium carbonate / N,N-dimethyl-formamide / 18 h / 70 °C

6.1: lithium hydroxide / tetrahydrofuran / 4 h / 45 °C

6.2: pH 3

With hydrogen; potassium carbonate; triethylamine; HATU; lithium hydroxide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene;

Reference yield:

: 874301-23-2
3-amino-5-chloro-2-nitrobenzoic acid methyl ester

: 1372540-75-4
1-[(3-chloro-2-methylphenyl)methyl]-2-(difluoromethyl)-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 110 °C

2.1: hydrogen / palladium on activated charcoal / methanol / 3 h / 20 °C / 3040.2 Torr / autoclave

3.1: toluene / 15 h / Reflux

4.1: potassium carbonate / N,N-dimethyl-formamide / 18 h / 70 °C

5.1: lithium hydroxide / tetrahydrofuran / 4 h / 45 °C

5.2: pH 3

With hydrogen; potassium carbonate; lithium hydroxide; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene;