(Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide

Base Information

Chemical Name:(Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide
CAS No.:1438409-29-0
Molecular Formula:C₂₁H₁₉N₃O₅S₂
Molecular Weight:457.531
Hs Code.:

Synonyms:(Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide

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Technology Process of (Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide

There total 4 articles about (Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide 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: 92.0%

: 1438408-95-7
(Z)-3-(2-aminoethyl)-5-(4-ethoxybenzylidene)thiazolidine-2,4-dione trifluoroacetate

: 49584-26-1
p-cyanobenzenesulfonyl chloride

: 1438409-29-0
(Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃;
DOI:10.1039/c3ob40199e

Reference yield:

: (Z)-5-(4-ethoxybenzylidene)thiazolidine-2,4-dione

: 1438409-29-0
(Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: triphenylphosphine / tetrahydrofuran / 0.08 h / 20 °C

1.2: 45 °C

2.1: dichloromethane / 0.5 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

With N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane;
DOI:10.1039/c3ob40199e

Reference yield:

: 1438408-80-0
C₃₃H₃₀N₂O₃S

: 1438409-29-0
(Z)-4-cyano-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 0.5 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

With N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1039/c3ob40199e