(2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile

Base Information

• Chemical Name: (2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile
• CAS No.: 1519005-24-3
• Molecular Formula: C₂₃H₂₁N₃O
• Molecular Weight: 355.439
• Mol file: 1519005-24-3.mol

Synonyms:(2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile

Chemical Property of (2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile

There total 3 articles about (2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile 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: 60.0%

1-cyanoacetylpiperidine (15029-30-8) + N-methyl-N-[(2-phenyl-1H-indol-3-yl)methylene]methanaminium chloride → (2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile (1519005-24-3)

Guidance literature:

With triethylamine; In N,N-dimethyl-formamide; at 80 - 90 ℃; for 0.75h; stereoselective reaction;

DOI:10.1016/j.tet.2013.10.086

Reference yield: 60.0%

1-cyanoacetylpiperidine (15029-30-8) + 2-phenyl-indole (948-65-2) + N,N-dimethyl-formamide (68-12-2,33513-42-7) → (2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile (1519005-24-3)

Guidance literature:

2-phenyl-indole; N,N-dimethyl-formamide; With benzoyl chloride; at 0 ℃;

1-cyanoacetylpiperidine; With triethylamine; In N,N-dimethyl-formamide; at 90 ℃; for 0.75h; stereoselective reaction;

DOI:10.1016/j.ejmech.2015.08.009

Reference yield:

2-phenyl-indole (948-65-2) → (2E)-3-(2-phenyl-1H-indol-3-yl)-2-(piperidin-1-ylcarbonyl)acrylonitrile (1519005-24-3)

Guidance literature:

Multi-step reaction with 2 steps

1: benzoyl chloride / 5 - 20 °C

2: triethylamine / N,N-dimethyl-formamide / 0.75 h / 80 - 90 °C

With benzoyl chloride; triethylamine; In N,N-dimethyl-formamide; 2: |Knoevenagel Condensation;

DOI:10.1016/j.tet.2013.10.086

upstream raw materials:

1-cyanoacetylpiperidine

2-phenyl-indole

N,N-dimethyl-formamide