{6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine

Base Information

• Chemical Name: {6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine
• CAS No.: 132751-87-2
• Molecular Formula: C₃₁H₃₇N₃O₂
• Molecular Weight: 483.654
• Mol file: 132751-87-2.mol

Synonyms:{6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine

Chemical Property of {6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine

There total 3 articles about {6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine 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:

2-Cyanopyridine (100-70-9,1232006-36-8) → {6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine (132751-87-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 85 percent / diethyl ether / 1 h / Heating

2: CaSO₄ / benzene / 24 h / Heating

With calcium sulfate; In diethyl ether; benzene;

DOI:10.1021/jm00111a033

Reference yield:

1-(6-bromohexyl)-5-methoxy-2-(4-methoxyphenyl)-3-methylindole (115084-37-2) → {6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine (132751-87-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 78 percent / dimethylformamide / 2 h / Heating

2: 45 percent / hydrazine hydrate / ethanol / 2 h / Heating

3: CaSO₄ / benzene / 24 h / Heating

With calcium sulfate; hydrazine hydrate; In ethanol; N,N-dimethyl-formamide; benzene;

DOI:10.1021/jm00111a033

Reference yield:

2-propionylpyridine (3238-55-9) + 1-(6-amino-hexyl)-5-methoxy-2-(4-methoxyphenyl)-3-methyl-indole (115084-42-9) → {6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-[1-pyridin-2-yl-prop-(E)-ylidene]-amine (132751-87-2)

Guidance literature:

With calcium sulfate; In benzene; for 24h; Heating;

DOI:10.1021/jm00111a033

upstream raw materials:

2-propionylpyridine

1-(6-amino-hexyl)-5-methoxy-2-(4-methoxyphenyl)-3-methyl-indole

2-Cyanopyridine

1-(6-bromohexyl)-5-methoxy-2-(4-methoxyphenyl)-3-methylindole

Downstream raw materials:

{6-[5-Methoxy-2-(4-methoxy-phenyl)-3-methyl-indol-1-yl]-hexyl}-(1-pyridin-2-yl-propyl)-amine

2-(4-Hydroxy-phenyl)-3-methyl-1-[6-(1-pyridin-2-yl-propylamino)-hexyl]-1H-indol-5-ol