(Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide

Base Information

Chemical Name:(Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide
CAS No.:1235459-01-4
Molecular Formula:C₂₈H₂₅Cl₂N₃O₅S
Molecular Weight:586.496
Hs Code.:

Synonyms:(Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide

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Chemical Property of (Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide

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Technology Process of (Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide

There total 4 articles about (Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide 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: 85.0%

: 1235458-26-0
(Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]-methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)propanoic acid

: 74-89-5
methylamine

: 1235459-01-4
(Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide

Guidance literature:: (Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]-methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)propanoic acid; With 1,1'-carbonyldiimidazole; In dichloromethane; at 20 ℃; for 3h;

methylamine; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1039/c4ra08720h

Reference yield:

: 477573-39-0
5-[(2,6-dichlorobenzyl)sulfonyl]-1,3-dihydro-2H-indol-2-one

: 1235459-01-4
(Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: piperidine / ethanol / 12 h / Reflux

2.1: 1,1'-carbonyldiimidazole / dichloromethane / 3 h / 20 °C

2.2: 12 h / 20 °C

With piperidine; 1,1'-carbonyldiimidazole; In ethanol; dichloromethane;
DOI:10.1039/c4ra08720h

Reference yield:

: C₁₂H₁₃NO₄

: 1235459-01-4
(Z)-3-(2-{[5-(2,6-dichlorobenzylsulfonyl)-2-oxoindolin-3-ylidene]methyl}-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-N-methylpropanamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: piperidine / ethanol / 12 h / Reflux

2.1: 1,1'-carbonyldiimidazole / dichloromethane / 3 h / 20 °C

2.2: 12 h / 20 °C

With piperidine; 1,1'-carbonyldiimidazole; In ethanol; dichloromethane;
DOI:10.1039/c4ra08720h