2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole

Base Information

• Chemical Name: 2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole
• CAS No.: 1081111-08-1
• Molecular Formula: C₂₉H₃₁ClN₄O
• Molecular Weight: 487.044
• Mol file: 1081111-08-1.mol

Synonyms:2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole

Chemical Property of 2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole

There total 6 articles about 2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole 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: 51.0%

→ 2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole (1081111-08-1)

Guidance literature:

Reference yield:

2-(4-chlorophenyl)benzimidazole (1019-85-8) + 3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl methanesulfonate (1081112-34-6) → 2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole (1081111-08-1)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 5h;

DOI:10.1016/j.bmcl.2011.02.099

Reference yield:

N1-(3-(piperidin-4-yl)phenyl)acetamide hydrochloride (486430-92-6) → 2-(4-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole (1081111-08-1)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 60 °C

2: triethylamine / dichloromethane / 3 h / 0 °C

3: potassium carbonate / N,N-dimethyl-formamide / 5 h / 80 °C

With potassium carbonate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2011.02.099

upstream raw materials:

N₁-(3-(piperidin-4-yl)phenyl)acetamide hydrochloride

3-[4-(3-acetylaminophenyl)piperidin-1-yl]propan-1-ol

2-(4-chlorophenyl)benzimidazole

3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl methanesulfonate

Downstream raw materials:

2-(4-chlorophenyl)-1-{3-[4-(3-aminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole

2-(4-chlorophenyl)-1-{3-[4-(3-isobutyrylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole

2-(4-chlorophenyl)-1-{3-[4-(3-benzoylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole

2-(4-chlorophenyl)-1-{3-[4-(3-(4-methylbenzoylamino)phenyl)piperidin-1-yl]propyl}-1H-benzimidazole