(E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

Base Information

Chemical Name:(E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid
CAS No.:1195961-03-5
Molecular Formula:C₂₃H₁₆BrClN₂O₃S₂
Molecular Weight:547.881
Hs Code.:

Synonyms:(E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

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Chemical Property of (E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

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Technology Process of (E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

There total 4 articles about (E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic 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: 81.0%

: 1195961-10-4
5-(4-bromo-3-chlorophenyl)thiophene-2-carbaldehyde

: 1195961-07-9
2-(5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

: 1195961-03-5
(E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

Guidance literature:: With acetic acid; 3-amino propanoic acid; at 170 ℃; for 0.5h; Microwave irradiation;

Reference yield:

: 1195961-09-1
2-(4-bromo-3-chlorophenyl)thiophene

: 1195961-03-5
(E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: trichlorophosphate / 1,2-dichloro-ethane / 0.33 h / 0 - 5 °C

1.2: 17 h / 10 °C / Reflux

2.1: acetic acid / 3-amino propanoic acid / 0.5 h / 170 °C / Microwave irradiation

With acetic acid; trichlorophosphate; 3-amino propanoic acid; In 1,2-dichloro-ethane; 2.1: Knoevenagel Condensation;

Reference yield:

: 721-66-4,104010-46-0
glycylphenylalanine

: 1195961-03-5
(E)-2-(4-((5-(4-bromo-3-chlorophenyl)thiophen-2-yl)methylene)-5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 16 h / Reflux

2: acetic acid / 3-amino propanoic acid / 0.5 h / 170 °C / Microwave irradiation

With acetic acid; N-ethyl-N,N-diisopropylamine; 3-amino propanoic acid; In tetrahydrofuran; 2: Knoevenagel Condensation;