3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester

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Chemical Name:3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester
CAS No.:210470-13-6
Molecular Formula:C₃₁H₂₅N₃O₆S
Molecular Weight:567.622
Hs Code.:

Synonyms:3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester

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Chemical Property of 3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester

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Technology Process of 3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester

There total 4 articles about 3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester 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%

: 1-benzenesulfonyl-3-tributylstannyl-1H-indole

: 3-[1-cyano-2-ethoxycarbonyl-2-(trifluoro-methanesulfonyloxy)-vinyl]-indole-1-carboxylic acid ethyl ester

: 210470-13-6
3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester

Guidance literature:: With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; lithium chloride; In tetrahydrofuran; for 3.5h; Heating;
DOI:10.1016/S0040-4020(98)00372-X

Reference yield:

: 3-cyano-2-hydroxy-3-(1H-indol-3-yl)-acrylic acid ethyl ester

: 210470-13-6
3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / TEA / CH₂Cl₂ / 0.17 h / 0 °C

2: 78 percent / Me₂NH / CH₂Cl₂ / 0.17 h / Ambient temperature

3: 85 percent / iPr₂NEt / CH₂Cl₂ / 0.08 h / 0 °C

4: 89 percent / Pd(Ph₃P)4, CuI, LiCl / tetrahydrofuran / 3.5 h / Heating

With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; TEA; dimethyl amine; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(98)00372-X

Reference yield:

: 210470-11-4
3-(1-cyano-2-ethoxycarbonyl-2-hydroxy-vinyl)-indole-1-carboxylic acid ethyl ester

: 210470-13-6
3-[2-(1-benzenesulfonyl-1H-indol-3-yl)-1-cyano-2-ethoxycarbonyl-vinyl]-indole-1-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / iPr₂NEt / CH₂Cl₂ / 0.08 h / 0 °C

2: 89 percent / Pd(Ph₃P)4, CuI, LiCl / tetrahydrofuran / 3.5 h / Heating

With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(98)00372-X