2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole

Base Information

Chemical Name:2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole
CAS No.:1610601-58-5
Molecular Formula:C₂₄H₁₇ClN₄O₂
Molecular Weight:428.878
Hs Code.:

Synonyms:2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole

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Chemical Property of 2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole

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Technology Process of 2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole

There total 7 articles about 2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole 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: 59.0%

: 351468-84-3
C₂₄H₁₉ClN₄O₂

: 1610601-58-5
2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole

Guidance literature:: With [bis(acetoxy)iodo]benzene; In dichloromethane; at 20 ℃;
DOI:10.1016/j.ejmech.2014.04.045

Reference yield:

: 1126-46-1
Methyl 4-chlorobenzoate

: 1610601-58-5
2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / ethanol / 16 h / Reflux

2: acetic acid / ethanol / 4 h / Reflux

3: [bis(acetoxy)iodo]benzene / dichloromethane / 20 °C

With [bis(acetoxy)iodo]benzene; hydrazine hydrate; acetic acid; In ethanol; dichloromethane;
DOI:10.1016/j.ejmech.2014.04.045

Reference yield:

: 74-11-3
para-chlorobenzoic acid

: 1610601-58-5
2-(4-chlorophenyl)-5-(3-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid / 12 h / Reflux

2: hydrazine hydrate / ethanol / 16 h / Reflux

3: acetic acid / ethanol / 4 h / Reflux

4: [bis(acetoxy)iodo]benzene / dichloromethane / 20 °C

With [bis(acetoxy)iodo]benzene; sulfuric acid; hydrazine hydrate; acetic acid; In ethanol; dichloromethane;
DOI:10.1016/j.ejmech.2014.04.045