5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one

Base Information

Chemical Name:5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one
CAS No.:1186634-25-2
Molecular Formula:C₁₂H₁₂N₄O₄S₂
Molecular Weight:340.384
Hs Code.:

Synonyms:5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one

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Chemical Property of 5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one

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Technology Process of 5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one

There total 6 articles about 5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one 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: 57.0%

: 1186634-24-1
((4-((3-methyl-4-oxo-1,3-thiazolidin-2-ylidene)amino)phenyl)(sulfamoyl)amino)acetic acid ethyl ester

: 1186634-25-2
5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one

Guidance literature:: With sodium hydroxide; In ethanol; water; for 1h;

Reference yield:

: 63500-84-5
3-methyl-2-(4-nitro-phenylimino)-thiazolidin-4-one

: 1186634-25-2
5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: iron; acetic acid / 5 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 20 - 60 °C

3.1: dichloromethane / 0.25 h / 0 °C

3.2: 1 h / 0 °C

4.1: trifluoroacetic acid / dichloromethane / 0 - 20 °C

5.1: sodium hydroxide / ethanol; water / 1 h

With iron; potassium carbonate; acetic acid; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1186634-21-8
2-(4-aminophenylimino)-3-methylthiazolidin-4-one

: 1186634-25-2
5-(4-(3-methyl-4-oxo-1,3-thiazolidin-2-ylideneamino)phenyl)-1,1-dioxo-1λ6-[1,2,5]thiadiazolidin-3-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 20 - 60 °C

2.1: dichloromethane / 0.25 h / 0 °C

2.2: 1 h / 0 °C

3.1: trifluoroacetic acid / dichloromethane / 0 - 20 °C

4.1: sodium hydroxide / ethanol; water / 1 h

With potassium carbonate; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;