ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate

Base Information

Chemical Name:ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate
CAS No.:1095274-49-9
Molecular Formula:C₁₇H₂₁ClN₄O₃
Molecular Weight:364.832
Hs Code.:

Synonyms:ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate

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Chemical Property of ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate

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Technology Process of ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate

There total 7 articles about ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate 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:

: 1095274-48-8
ethyl 3-(2-{[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]carbonyl}hydrazino)-3-oxopropanoate

: 1095274-49-9
ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate

Guidance literature:: With Burgess Reagent; In dichloromethane; at 100 ℃; for 0.166667h; Microwave irradition;

Reference yield:

: 896466-67-4
3-chloro-5-(4-methylpiperazin-1-yl)benzonitrile

: 1095274-49-9
ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide / ethanol; water / 2.5 h / Heating / reflux

2.1: sulfuric acid / 96 h / Heating / reflux

2.2: 20 °C / pH 7 - 8

3.1: hydrazine / ethanol / 4 h / Heating / reflux

4.1: tetrahydrofuran / 0.5 h / 20 °C

5.1: Burgess Reagent / dichloromethane / 0.17 h / 100 °C / Microwave irradition

With sodium hydroxide; Burgess Reagent; sulfuric acid; hydrazine; In tetrahydrofuran; ethanol; dichloromethane; water;

Reference yield:

: 327056-73-5
3-fluoro-5-chlorobenzonitrile

: 1095274-49-9
ethyl {5-[3-chloro-5-(4-methyl-1-piperazinyl)phenyl]-1,3,4-oxadiazol-2-yl}acetate

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / dimethyl sulfoxide / 20 - 80 °C

2.1: sodium hydroxide / ethanol; water / 2.5 h / Heating / reflux

3.1: sulfuric acid / 96 h / Heating / reflux

3.2: 20 °C / pH 7 - 8

4.1: hydrazine / ethanol / 4 h / Heating / reflux

5.1: tetrahydrofuran / 0.5 h / 20 °C

6.1: Burgess Reagent / dichloromethane / 0.17 h / 100 °C / Microwave irradition

With sodium hydroxide; Burgess Reagent; sulfuric acid; potassium carbonate; hydrazine; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide;