4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide

Base Information

Chemical Name:4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide
CAS No.:1480838-52-5
Molecular Formula:C₂₂H₂₁N₃O₄
Molecular Weight:391.426
Hs Code.:

Synonyms:4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide

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Chemical Property of 4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide

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Technology Process of 4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide

There total 7 articles about 4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide 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: 56.0%

: 1478592-87-8
C₂₉H₂₇N₃O₄

: 1480838-52-5
4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide

Guidance literature:: With boron trichloride; In dichloromethane; at -10 ℃; for 1h;
DOI:10.1021/cb400067g

Reference yield:

: 728878-27-1
4-[(4'-aminophenyl)buta-1,3-diyn-1-yl]benzoic acid

: 1480838-52-5
4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: dicyclohexyl-carbodiimide; dmap / tetrahydrofuran / 12 h / 20 °C

2: triethylamine / N,N-dimethyl-formamide / 12 h / 20 °C

3: boron trichloride / dichloromethane / 1 h / -10 °C

With dmap; boron trichloride; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/cb400067g

Reference yield:

: 1139694-89-5
methyl (2R,3S,7R,7aS)-7-methoxy-2,3,7,7a-tetramethyl-5-oxotetrahydro-2H-oxazolo[4,3-b]oxazole-3-carboxylate

: 1480838-52-5
4-((4-aminophenyl)buta-1,3-diynyl)-N-(3-hydroxy-1-(hydroxyamino)-2-methyl-1-oxobutan-2-yl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

2: hydrogenchloride / water; methanol / 12 h / 20 °C / Reflux

3: triethylamine / N,N-dimethyl-formamide / 12 h / 20 °C

4: boron trichloride / dichloromethane / 1 h / -10 °C

With hydrogenchloride; boron trichloride; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/cb400067g