(S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid

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Chemical Name:(S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid
CAS No.:1393891-50-3
Molecular Formula:C₂₉H₂₂N₂O₅S₂
Molecular Weight:542.636
Hs Code.:

Synonyms:(S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid

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Chemical Property of (S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid

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Technology Process of (S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid

There total 2 articles about (S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid 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: 54.0%

: (S)-3-(1H-indol-3-yl)-2-(4-oxo-2-thioxothiazolidin-3-yl)propanoic acid

: 139484-40-5
ω-(4-formylphenoxy)acetophenone

: 1393891-50-3
(S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid

Guidance literature:: With piperidine; acetic acid; In ethanol; for 4h; Reflux;
DOI:10.1016/j.ejmech.2012.05.023

Reference yield:

: 70-11-1
α-bromoacetophenone

: 1393891-50-3
(S,Z)-3-(1H-indol-3-yl)-2-(4-oxo-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-3-yl)propanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 20 °C

2: piperidine; acetic acid / ethanol / 4 h / Reflux

With piperidine; acetic acid; In ethanol; acetone; 2: Knoevenagel condensation;
DOI:10.1016/j.ejmech.2012.05.023