9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole

Base Information

• Chemical Name: 9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole
• CAS No.: 1146473-29-1
• Molecular Formula: C₃₆H₃₄N₂
• Molecular Weight: 494.679
• Mol file: 1146473-29-1.mol

Synonyms:9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole

Chemical Property of 9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

Useful:

Technology Process of 9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole

There total 3 articles about 9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole 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: 96.0%

1-benzyl-5-methyl-2-vinyl-1H-indole (1146472-99-2) → 9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole (1146473-29-1)

Guidance literature:

With 2-iodoimidazolinium triflate; In chloroform; at 20 ℃; for 19h; Inert atmosphere;

DOI:10.1002/anie.201904689

Reference yield: 23.0%

1-benzyl-5-methyl-2-vinyl-1H-indole (1146472-99-2) + 1-benzyl-5-methoxy-2-vinyl-1H-indole (1146472-93-6) → 9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole (1146473-29-1) + 9-benzyl-3-(1-benzyl-5-methoxy-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole (1146473-55-3) + 9-benzyl-3-(1-benzyl-5-methoxy-1H-indol-2-yl)-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole (1146473-24-6)

Guidance literature:

With trifluoroacetic acid; In dichloromethane; at 20 ℃;

DOI:10.1021/jo900104r

Reference yield:

C17H15NO (1287693-74-6) → 9-benzyl-3-(1-benzyl-5-methyl-1H-indol-2-yl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole (1146473-29-1)

Guidance literature:

Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / 0 °C / Inert atmosphere

1.2: 1 h / 0 °C / Inert atmosphere

2.1: 2-iodoimidazolinium triflate / chloroform / 19 h / 20 °C / Inert atmosphere

With n-butyllithium; 2-iodoimidazolinium triflate; In tetrahydrofuran; hexane; chloroform;

DOI:10.1002/anie.201904689

upstream raw materials:

1-benzyl-5-methyl-2-vinyl-1H-indole

1-benzyl-5-methoxy-2-vinyl-1H-indole

C₁₇H₁₅NO