3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine

Base Information

Chemical Name:3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine
CAS No.:1379946-06-1
Molecular Formula:C₂₃H₂₂ClN₅O
Molecular Weight:419.914
Hs Code.:

Synonyms:3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine

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Chemical Property of 3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine

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Technology Process of 3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine

There total 3 articles about 3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine 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:

: 1379946-64-1,801303-19-5
(Z)-N-hydroxy-2-(methylamino)nicotinimidamide

: 1105624-44-9
2-(3-chlorophenyl)-2-((3,4-dimethylphenyl)amino)acetic acid

: 1379946-06-1
3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine

Guidance literature:: With 1,1'-carbonyldiimidazole; In 1,2-dichloro-ethane; at 95 ℃; for 14h;

Reference yield:

: 1878-65-5
3-chlorophenylacetic acid

: 1379946-06-1
3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 5 h / Reflux

2.1: sulfuric acid / 3 h / Reflux

3.1: potassium carbonate / butanone / 14 h / 80 °C

3.2: 6 h / Reflux

4.1: 1,1'-carbonyldiimidazole / 1,2-dichloro-ethane / 14 h / 95 °C

With N-Bromosuccinimide; sulfuric acid; potassium carbonate; 1,1'-carbonyldiimidazole; dibenzoyl peroxide; In tetrachloromethane; 1,2-dichloro-ethane; butanone;

Reference yield:

: 3381-74-6
α-Bromo-(3-chlorophenyl)acetic acid

: 1379946-06-1
3-(5-((3-chlorophenyl)((3,4-dimethylphenyl)amino)methyl)-1,2,4-oxadiazol-3-yl)-N-methylpyridin-2-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: sulfuric acid / 3 h / Reflux

2.1: potassium carbonate / butanone / 14 h / 80 °C

2.2: 6 h / Reflux

3.1: 1,1'-carbonyldiimidazole / 1,2-dichloro-ethane / 14 h / 95 °C

With sulfuric acid; potassium carbonate; 1,1'-carbonyldiimidazole; In 1,2-dichloro-ethane; butanone;