(Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

Base Information

Chemical Name:(Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide
CAS No.:1438409-30-3
Molecular Formula:C₁₈H₂₀N₄O₅S₂
Molecular Weight:436.513
Hs Code.:

Synonyms:(Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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Chemical Property of (Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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Technology Process of (Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

There total 4 articles about (Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide 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: 98.0%

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

: 137049-00-4
1-methyl-1H-imidazole-4-sulfonyl chloride

: 1438409-30-3
(Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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

: 1438409-30-3
(Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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

: 1438409-30-3
(Z)-N-(2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)-1-methyl-1H-imidazole-4-sulfonamide

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