4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione

Base Information

• Chemical Name: 4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione
• CAS No.: 794547-85-6
• Molecular Formula: C₂₉H₃₂N₂O₃
• Molecular Weight: 456.585

Synonyms:4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione

Chemical Property of 4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione

Chemical Property:

Purity/Quality:

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Technology Process of 4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione

There total 4 articles about 4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-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: 89.0%

allyl bromide (106-95-6) + 2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione (794547-79-8) → 4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione (794547-85-6)

Guidance literature:

With sodium hydride; In tetrahydrofuran; at 20 ℃; for 16h;

DOI:10.1016/j.tet.2004.07.069

Reference yield:

bromopentene (1119-51-3) → 4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione (794547-85-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 59 percent / K₂CO₃ / acetone / 48 h / Heating

2: 97 percent / LiOH*H₂O / ethanol; H₂O / 0.5 h / Heating

3: 89 percent / NaH / tetrahydrofuran / 16 h / 20 °C

With lithium hydroxide; sodium hydride; potassium carbonate; In tetrahydrofuran; ethanol; water; acetone;

DOI:10.1016/j.tet.2004.07.069

Reference yield:

ethyl 5-hydroxy-2-(4-methoxybenzyl)-10-methyl-1-oxo-1,2,3,10-tetrahydroazepino[3,4-b]indole-4-carboxylate (794547-72-1) → 4-allyl-2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione (794547-85-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 59 percent / K₂CO₃ / acetone / 48 h / Heating

2: 97 percent / LiOH*H₂O / ethanol; H₂O / 0.5 h / Heating

3: 89 percent / NaH / tetrahydrofuran / 16 h / 20 °C

With lithium hydroxide; sodium hydride; potassium carbonate; In tetrahydrofuran; ethanol; water; acetone;

DOI:10.1016/j.tet.2004.07.069

upstream raw materials:

allyl bromide

2-(4-methoxybenzyl)-10-methyl-4-(4-pentenyl)-3,4-dihydroazepino[3,4-b]indole-1,5(2H,10H)-1,5-dione

bromopentene

ethyl 5-hydroxy-2-(4-methoxybenzyl)-10-methyl-1-oxo-1,2,3,10-tetrahydroazepino[3,4-b]indole-4-carboxylate

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