2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide

Base Information

Chemical Name:2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide
CAS No.:332870-17-4
Molecular Formula:C₁₉H₁₇N₅O₂S
Molecular Weight:379.442
Hs Code.:

Synonyms:2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide

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Chemical Property of 2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide

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Technology Process of 2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide

There total 6 articles about 2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide 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: 71.0%

: 332128-57-1
5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazole-2-thiol

: 16634-82-5
N-(p-tolyl)-2-chloroacetamide

: 332870-17-4
2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide

Guidance literature:: With potassium carbonate; In acetone; Reflux;
DOI:10.1016/j.ejmech.2012.03.033

Reference yield:

: 106-49-0,12221-03-3
p-toluidine

: 332870-17-4
2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetone / Reflux

2: potassium carbonate / acetone / Reflux

With potassium carbonate; In acetone;
DOI:10.1016/j.ejmech.2012.03.033

Reference yield:

: 95-54-5
1,2-diamino-benzene

: 332870-17-4
2-(5-((1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazol-2-ylthio)-N-p-tolylacetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 2 h / 100 °C

1.2: 20 °C

2.1: sodium hydroxide / methanol / 0.5 h / Reflux

3.1: hydrazine hydrate / ethanol / Reflux

4.1: potassium hydroxide / ethanol / 0 °C / Reflux

5.1: potassium carbonate / acetone / Reflux

With potassium carbonate; hydrazine hydrate; potassium hydroxide; sodium hydroxide; In methanol; ethanol; acetone;
DOI:10.1016/j.ejmech.2012.03.033