2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide

Base Information

Chemical Name:2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide
CAS No.:1329118-28-6
Molecular Formula:C₂₉H₂₅ClFN₅O₂
Molecular Weight:530.001
Hs Code.:

Synonyms:2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide

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Chemical Property of 2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide

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Technology Process of 2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide

There total 8 articles about 2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide 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: 28.0%

: 1254171-21-5
2-(2-chloro-6-fluoro-phenyl)-1H-imidazole-4-carboxylic acid

: 1329119-56-3
6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-ylamine

: 1329118-28-6
2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 100-39-0
benzyl bromide

: 1329118-28-6
2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide

Guidance literature:: Multi-step reaction with 5 steps

1: caesium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide

2: ethanol / 24 h / 50 °C

3: hydrogen / tetrahydrofuran / 4 h / 1551.49 Torr

4: methanol / 24 h / 20 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C

With hydrogen; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 394-41-2
3-fluoro-4-nitrophenol

: 1329118-28-6
2-(2-chloro-6-fluorophenyl)-1H-imidazole-4-carboxylic acid (6-benzyloxy-1-cyclopentyl-1H-benzimidazol-2-yl)amide

Guidance literature:: Multi-step reaction with 5 steps

1: caesium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide

2: ethanol / 24 h / 50 °C

3: hydrogen / tetrahydrofuran / 4 h / 1551.49 Torr

4: methanol / 24 h / 20 °C

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C

With hydrogen; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide;