?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide

Base Information

Chemical Name:?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide
CAS No.:1429303-04-7
Molecular Formula:C₂₂H₁₉N₃O₅S
Molecular Weight:437.476
Hs Code.:

Synonyms:?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide

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Chemical Property of ?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide

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Technology Process of ?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide

There total 4 articles about ?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide 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: 84.0%

: 69321-32-0
2-(2-(4-methyl-2-oxo-2H-chromen-7-yloxy)acetyl)-N-p-tolylhydrazinecarbothioamide

: 105-36-2
ethyl bromoacetate

: 1429303-04-7
?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide

Guidance literature:: With sodium acetate; In ethanol; for 9h; Reflux;
DOI:10.1016/j.foodchem.2013.01.027

Reference yield:

: 90-33-5,79566-13-5
7-hydroxy-4-methyl-chromen-2-one

: 1429303-04-7
?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / acetone

2: hydrazine

3: ethanol / 3 h / Reflux

4: sodium acetate / ethanol / 9 h / Reflux

With sodium acetate; potassium carbonate; hydrazine; In ethanol; acetone;
DOI:10.1016/j.foodchem.2013.01.027

Reference yield:

: 5614-82-4
ethyl 2-(4-methyl-2-oxo-2-coumarin-7-yloxy)acetate

: 1429303-04-7
?(Z)-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N-(4-oxo-2-(p-tolylimino)thiazolidin-3-yl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine

2: ethanol / 3 h / Reflux

3: sodium acetate / ethanol / 9 h / Reflux

With sodium acetate; hydrazine; In ethanol;
DOI:10.1016/j.foodchem.2013.01.027