1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile

Base Information

• Chemical Name: 1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile
• CAS No.: 1542257-07-7
• Molecular Formula: C₂₂H₁₄N₈O₃
• Molecular Weight: 438.405
• Mol file: 1542257-07-7.mol

Synonyms:1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile

Chemical Property of 1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile

There total 2 articles about 1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile 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: 71.0%

3-nitrobenzylidenemalononitrile (2826-32-6) + N′-(1-(1H-benzo[d]imidazol-2-yl)ethylidene)-2-cyanoacetohydrazide (1338245-65-0) → 1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile (1542257-07-7)

Guidance literature:

With piperidine; In ethanol; for 3h; Reflux;

DOI:10.1016/j.cclet.2013.11.026

Reference yield:

2-acetylbenzimidazole (939-70-8) → 1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile (1542257-07-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 1,4-dioxane / 3 h / Reflux

2: piperidine / ethanol / 3 h / Reflux

With piperidine; In 1,4-dioxane; ethanol;

DOI:10.1016/j.cclet.2013.11.026

Reference yield: 64.0%

1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-amino-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile (1542257-07-7) + 3-Fluorobenzaldehyde (456-48-4) → 1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-((3-fluorobenzylidene)amino)-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile (1542257-10-2)

Guidance literature:

In ethanol; for 5h; Reflux;

DOI:10.1016/j.cclet.2013.11.026

upstream raw materials:

2-acetylbenzimidazole

3-nitrobenzylidenemalononitrile

N′-(1-(1H-benzo[d]imidazol-2-yl)ethylidene)-2-cyanoacetohydrazide

Downstream raw materials:

1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-((benzylidene)amino)-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile

1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-((3-fluorobenzylidene)amino)-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile

1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-((4-fluorobenzylidene)amino)-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile

1-((1-(1H-benzo[d]imidazol-2-yl)ethylidene)amino)-6-((3-methylbenzylidene)amino)-4-(3-nitrophenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile