1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-

Base Information

• Chemical Name: 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-
• CAS No.: 160256-37-1
• Molecular Formula: C34H35N3O4Si
• Molecular Weight: 577.755
• Mol file: 160256-37-1.mol

Synonyms:

Chemical Property of 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-

There total 6 articles about 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]- 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: 75.0%

1-<(benzyloxy)methyl>-4-bromo-3,4-dihydro-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione (160256-36-0) → 1-<(benzyloxy)methyl>-3,4-dihydro-4-(1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione (160256-37-1)

Guidance literature:

In benzene; at 0 - 20 ℃;

DOI:10.1021/ja00106a072

Reference yield:

indole (120-72-9) → 1-<(benzyloxy)methyl>-3,4-dihydro-4-(1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione (160256-37-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 1.) MeMgI / 1.) benzene, Et₂O, 1 h, 2.) benzene, Et₂O, RT, overnight

2: 1.) NaH / 1.) THF, RT, 20 min, 2.) THF, 1 h

3: 1.) MeMgI / 1.) C₆H₆, Et₂O, RT, 1 h, 2.) C₆H₆, Et₂O, RT, overnight

With methyl magnesium iodide; sodium hydride;

DOI:10.1021/ja952907g

Reference yield:

(2-trimethylethylsilylethoxy)methyl chloride (76513-69-4) → 1-<(benzyloxy)methyl>-3,4-dihydro-4-(1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione (160256-37-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) NaH / 1.) THF, RT, 20 min, 2.) THF, 1 h

2: 1.) MeMgI / 1.) C₆H₆, Et₂O, RT, 1 h, 2.) C₆H₆, Et₂O, RT, overnight

With methyl magnesium iodide; sodium hydride;

DOI:10.1021/ja952907g

upstream raw materials:

indole

1-<(benzyloxy)methyl>-4-bromo-3,4-dihydro-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione

(2-trimethylethylsilylethoxy)methyl chloride

N-benzyloxymethyl-3,4-dibromomaleimide

Downstream raw materials:

1-<(benzyloxy)methyl>-3,4-dihydro-4-(<3-<<(benzyloxy)methyl>amino>-3-N,4-O-carbonyl-6-O-(4-methoxybenzyl)-α-D-altropyranosyl>-1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione

C₂₇H₂₄N₄O₃

staurosporine