N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide

Base Information

Chemical Name:N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide
CAS No.:1357597-97-7
Molecular Formula:C₂₆H₁₉N₅O₃S
Molecular Weight:481.535
Hs Code.:

Synonyms:N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide

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Chemical Property of N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide

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Technology Process of N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide

There total 4 articles about N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-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: 74.0%

: C₁₈H₁₃N₅O₂S

: 532-27-4,108321-66-0,164322-25-2
1-chloroacetophenone

: 1357597-97-7
N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide

Guidance literature:: With triethylamine; In ethanol; for 2h; Reflux;
DOI:10.1016/j.ejmech.2011.12.013

Reference yield:

: 1357598-10-7
N-(5-(cyanomethyl)-1,3,4-oxadiazol-2-yl)benzamide

: 1357597-97-7
N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / N,N-dimethyl-formamide / 6 h

1.2: Cooling with ice

2.1: triethylamine / ethanol / 2 h / Reflux

With triethylamine; potassium hydroxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.12.013

Reference yield:

: 103-72-0
phenyl isothiocyanate

: 1357597-97-7
N-(5-(4-amino-5-benzoyl-2-(phenylamino)thiophen-3-yl)1,3,4-oxadiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / N,N-dimethyl-formamide / 6 h

1.2: Cooling with ice

2.1: triethylamine / ethanol / 2 h / Reflux

With triethylamine; potassium hydroxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.12.013