(Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)

Base Information

Chemical Name:(Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)
CAS No.:130437-05-7
Molecular Formula:C₁₉H₁₉N₃O₉
Molecular Weight:433.375
Hs Code.:

Synonyms:(Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)

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Chemical Property of (Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)

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Technology Process of (Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)

There total 4 articles about (Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide) 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: 69.0%

: 33524-89-9
3,5-diacetyltetrahydropyran-2,4,6-trione

: 116193-71-6
N-[3-Amino-5-(2-hydroxy-acetylamino)-phenyl]-2-hydroxy-acetamide

: 130437-05-7
(Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)

Guidance literature:: In methanol; for 1.5h; Heating;
DOI:10.1021/jm00105a060

Reference yield:

: 5042-55-7
5-nitrobenzene-1,3-diamine

: 130437-05-7
(Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)

Guidance literature:: Multi-step reaction with 4 steps

1: 78 percent / dicyclohexylcarbodiimide (DCC), pyridine / CH₂Cl₂ / 1.) 0 deg C, 1 h, 2.) 25 deg C, 2 h

2: 75 percent / CF₃CO₂H / CHCl₃; various solvent(s) / 17 h / Heating

3: 77 percent / H₂ / 10percent Pd/C / 20 h / 1551.4 Torr

4: 69 percent / methanol / 1.5 h / Heating

With pyridine; hydrogen; dicyclohexyl-carbodiimide; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; chloroform;
DOI:10.1021/jm00105a060

Reference yield:

: 116193-70-5
3,5-bis(2-hydroxyacetamido)nitrobenzene

: 130437-05-7
(Z)-N,N'-(5-{[1-(5-acetyl-4-hydroxy-2,6-dioxo-2H-pyran-3(6H)-ylidene)ethyl]amino}-1,3-phenylene)bis(2-hydroxyacetamide)

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / H₂ / 10percent Pd/C / 20 h / 1551.4 Torr

2: 69 percent / methanol / 1.5 h / Heating

With hydrogen; palladium on activated charcoal; In methanol;
DOI:10.1021/jm00105a060