(Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

Base Information

Chemical Name:(Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile
CAS No.:1329121-24-5
Molecular Formula:C₂₀H₁₁N₃O₂S₂
Molecular Weight:389.458
Hs Code.:

Synonyms:(Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

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Chemical Property of (Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

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Technology Process of (Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

There total 5 articles about (Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile 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: 91.0%

: 7269-72-9
3-indolylglyoxal

: 401604-21-5
4-(4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

: 1329121-24-5
(Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

Guidance literature:: With 2,2,6,6-tetramethyl-piperidine; In ethanol; at 90 ℃; for 0.25h; under 7757.43 Torr; diastereoselective reaction; Microwave irradiation;
DOI:10.1016/j.tetlet.2011.05.114

Reference yield: 91.0%

: 1329121-24-5
(Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

Guidance literature:: With 2,2,6,6-tetramethyl-piperidine; In ethanol; at 90 ℃; for 0.25h; under 7757.43 Torr; Microwave irradiation;

Reference yield:

: 22980-09-2
indolyl-3-glyoxylyl chloride

: 1329121-24-5
(Z)-4-(5-(2-(1H-indol-3-yl)-2-oxoethylidene)-4-oxo-2-thioxothiazolidin-3-yl)benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: tri-n-butyl-tin hydride / 0 - 20 °C

2: 2,2,6,6-tetramethyl-piperidine / ethanol / 0.25 h / 90 °C / 7757.43 Torr / Microwave irradiation

With 2,2,6,6-tetramethyl-piperidine; tri-n-butyl-tin hydride; In ethanol; 2: Knoevenagel condensation;
DOI:10.1016/j.tetlet.2011.05.114