1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione

Base Information

• Chemical Name: 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione
• CAS No.: 1456901-37-3
• Molecular Formula: C₂₄H₂₃N₅O₆
• Molecular Weight: 477.477
• Mol file: 1456901-37-3.mol

Synonyms:1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione

Chemical Property of 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione

There total 5 articles about 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione 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: 99.0%

2-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione (1456901-35-1) → 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione (1456901-37-3)

Guidance literature:

With methoxybenzene; at 120 ℃; for 1.5h; Inert atmosphere;

DOI:10.1246/cl.130235

Reference yield:

1-(5-methoxy-2-nitro-4-(prop-2-yn-1-yloxy)phenyl)ethan-1-one (1255792-04-1) → 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione (1456901-37-3)

Guidance literature:

Multi-step reaction with 5 steps

1.1: sodium tetrahydroborate / tetrahydrofuran; methanol / 1 h / 0 °C

2.1: phosphorus tribromide; pyridine / tetrahydrofuran; benzene / 12.5 h / 0 °C / Inert atmosphere

3.1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h

3.2: 3 h / 50 °C / Inert atmosphere

4.1: copper(I) bromide; N,N,N',N'',N'''-pentamethyldiethylenetriamine / N,N-dimethyl-formamide / 20 h / 20 °C / Inert atmosphere

5.1: methoxybenzene / 1.5 h / 120 °C / Inert atmosphere

With pyridine; sodium tetrahydroborate; N,N,N',N'',N'''-pentamethyldiethylenetriamine; phosphorus tribromide; potassium carbonate; methoxybenzene; copper(I) bromide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; benzene; 4.1: |Huisgen Cycloaddition;

DOI:10.1246/cl.130235

Reference yield:

3-(2-methoxy-5-nitro-4-(1-(oxabicyclo[2,2,1]hept-5-enedicarboxyimide)ethyl)phenoxy)-1-propyne (1255792-08-5) → 1-(1-(5-methoxy-2-nitro-4-((1-(1-phenylethyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)ethyl)-1H-pyrrole-2,5-dione (1456901-37-3)

Guidance literature:

Multi-step reaction with 2 steps

1: copper(I) bromide; N,N,N',N'',N'''-pentamethyldiethylenetriamine / N,N-dimethyl-formamide / 20 h / 20 °C / Inert atmosphere

2: methoxybenzene / 1.5 h / 120 °C / Inert atmosphere

With N,N,N',N'',N'''-pentamethyldiethylenetriamine; methoxybenzene; copper(I) bromide; In N,N-dimethyl-formamide; 1: |Huisgen Cycloaddition;

DOI:10.1246/cl.130235

upstream raw materials:

1-(5-methoxy-2-nitro-4-(prop-2-yn-1-yloxy)phenyl)ethan-1-one

1-(5-methoxy-2-nitro-4-(prop-2-yn-1-yloxy)phenyl)ethan-1-ol

1-(5-methoxy-2-nitro-4-prop-2-ynyloxyphenyl)ethyl bromide

3-(2-methoxy-5-nitro-4-(1-(oxabicyclo[2,2,1]hept-5-enedicarboxyimide)ethyl)phenoxy)-1-propyne