3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione

Base Information

• Chemical Name: 3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione
• CAS No.: 1020475-54-0
• Molecular Formula: C₂₆H₁₈ClN₃O₂S
• Molecular Weight: 471.967
• Mol file: 1020475-54-0.mol

Synonyms:3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione

Chemical Property of 3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione

There total 3 articles about 3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione 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: 82.0%

3-benzylthiazolin-2,4-dione (37868-80-7) + 1-phenyl-3-(4-chlorophenyl)-4-pyrazolecarboxaldehyde (36663-00-0) → 3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione (1020475-54-0)

Guidance literature:

With piperidine; acetic acid; In toluene; for 20h; Reflux;

DOI:10.1016/j.bmc.2010.01.021

Reference yield:

phenylhydrazine (100-63-0) → 3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione (1020475-54-0)

Guidance literature:

Multi-step reaction with 3 steps

1: acetic acid / ethanol

2: trichlorophosphate

3: acetic acid; piperidine / ethanol / Reflux

With piperidine; acetic acid; trichlorophosphate; In ethanol; 2: |Vilsmeier-Haack Formylation / 3: |Knoevenagel Condensation;

DOI:10.1016/j.bioorg.2019.103271

Reference yield:

para-chloroacetophenone (99-91-2) → 3-benzyl-5-((3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-dione (1020475-54-0)

Guidance literature:

Multi-step reaction with 3 steps

1: acetic acid / ethanol

2: trichlorophosphate

3: acetic acid; piperidine / ethanol / Reflux

With piperidine; acetic acid; trichlorophosphate; In ethanol; 2: |Vilsmeier-Haack Formylation / 3: |Knoevenagel Condensation;

DOI:10.1016/j.bioorg.2019.103271

upstream raw materials:

3-benzylthiazolin-2,4-dione

1-phenyl-3-(4-chlorophenyl)-4-pyrazolecarboxaldehyde

phenylhydrazine

para-chloroacetophenone