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

Base Information

Chemical Name:1-<(benzyloxy)methyl>-3,4-dihydro-4-(<3-<<(benzyloxy)methyl>amino>-3-N,4-O-carbonyl-6-O-(4-methoxybenzyl)-2-O-<(pentafluorophenoxy)thiocarbonyl>-α-D-altropyranosyl>-1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dion
CAS No.:174290-92-7
Molecular Formula:C₆₄H₅₉F₅N₄O₁₂SSi
Molecular Weight:1231.34
Hs Code.:

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

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

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

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

There total 2 articles about 1-<(benzyloxy)methyl>-3,4-dihydro-4-(<3-<<(benzyloxy)methyl>amino>-3-N,4-O-carbonyl-6-O-(4-methoxybenzyl)-2-O-<(pentafluorophenoxy)thiocarbonyl>-α-D-altropyranosyl>-1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dion 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:

: 463-71-8
thiophosgene

: 771-61-9
2,3,4,5,6-pentafluorophenol

: 174290-90-5
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

: 174290-92-7
1-<(benzyloxy)methyl>-3,4-dihydro-4-(<3-<<(benzyloxy)methyl>amino>-3-N,4-O-carbonyl-6-O-(4-methoxybenzyl)-2-O-<(pentafluorophenoxy)thiocarbonyl>-α-D-altropyranosyl>-1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dion

Guidance literature:: With pyridine; dmap; Multistep reaction; 1.) CH₂Cl₂, reflux, 2.) CH₂Cl₂, reflux;
DOI:10.1021/ja00106a072

Reference yield:

: 463-71-8
thiophosgene

: 771-61-9
2,3,4,5,6-pentafluorophenol

: 1-Benzyloxymethyl-3-{1-[(3aS,4R,7aS)-1-benzyloxymethyl-7-hydroxy-4-(4-methoxy-benzyloxymethyl)-2-oxo-hexahydro-pyrano[4,3-d]oxazol-6-yl]-1H-indol-3-yl}-4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indol-3-yl]-pyrrole-2,5-dione

: 174290-92-7
1-<(benzyloxy)methyl>-3,4-dihydro-4-(<3-<<(benzyloxy)methyl>amino>-3-N,4-O-carbonyl-6-O-(4-methoxybenzyl)-2-O-<(pentafluorophenoxy)thiocarbonyl>-α-D-altropyranosyl>-1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dion

: 1-[(benzyloxy)methyl]-3,4-dihydro-4-[(3-{[(benzyloxy)methyl]amino}-3-N,4-O-carbonyl-6-O-(4-methoxybenzyl)-2-O-[(pentafluorophenoxy)thiocarbonyl]-β-D-allopyranoside)-1H-indol-3-yl]-3-{1-[2-(trimethylsilyl)ethoxymethyl]-1H-indol-3-yl}-1H-pyrrole-2,5-dion

Guidance literature:: With pyridine; dmap; Yield given. Multistep reaction. Yields of byproduct given; 1.) CH₂Cl₂, reflux, 4 h, 2.) CH₂Cl₂, reflux, 4 h;
DOI:10.1021/ja952907g