4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one

Base Information

Chemical Name:4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one
CAS No.:1357181-56-6
Molecular Formula:C₃₀H₂₈N₂O₇S₂
Molecular Weight:592.694
Hs Code.:

Synonyms:4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one

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Chemical Property of 4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one

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Technology Process of 4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one

There total 8 articles about 4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one 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: 78.0%

: 1357181-46-4
(2E,4E)-3-ethoxycarbonyl-5-(n-p-toluenesulfonyl-3-indolyl)-N-(p-toluenesulfonyl)-2,4-pentadienamide

: 1357181-56-6
4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 1,2-bis-(diphenylphosphino)ethane; In toluene; at 100 ℃; for 1h; Inert atmosphere;
DOI:10.1021/ol300737t

Reference yield:

: 1357181-62-4
(Z)-4-ethoxy-3-iodo-4-oxobut-2-enoic acid

: 1357181-56-6
4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 4-methyl-morpholine / tetrahydrofuran / 0.17 h / 0 °C

1.2: 0.25 h / 0 °C

2.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h / 0 °C

2.2: 2 h / 0 - 20 °C

3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / 1 h / 80 °C

4.1: o-xylene / 3 h / 130 °C

With 4-methyl-morpholine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium hydride; In tetrahydrofuran; 1,4-dioxane; o-xylene; mineral oil; 3.1: Migita-Stille coupling;
DOI:10.1016/j.tetlet.2011.12.014

Reference yield:

: 1373869-69-2
C₁₁H₁₅IO₆

: 1357181-56-6
4-ethoxycarbonyl-6-(n-p-toluenesulfonyl-3-indolyl)-1-(p-toluenesulfonyl)-1,6-dihydropyridin-2(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.17 h / 0 °C

1.2: 2 h / 0 - 20 °C

2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / 1 h / 80 °C

3.1: o-xylene / 3 h / 130 °C

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium hydride; In tetrahydrofuran; 1,4-dioxane; o-xylene; mineral oil; 2.1: Migita-Stille coupling;
DOI:10.1016/j.tetlet.2011.12.014