{3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester

Base Information

Chemical Name:{3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester
CAS No.:1345042-07-0
Molecular Formula:C₂₁H₁₉ClN₄O₃
Molecular Weight:410.86
Hs Code.:

Synonyms:{3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester

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Chemical Property of {3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester

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Technology Process of {3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester

There total 7 articles about {3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester 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%

: 1345041-83-9
5-(4-chlorophenyl)-N-hydroxy-1-phenyl-4,5-dihydro-1H-pyrazole-3-carboxamidine

: 36239-09-5
ethyl chlorocarbonylacetate

: 1345042-07-0
{3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester

Guidance literature:: With pyridine; at 0 - 100 ℃; Inert atmosphere;
DOI:10.1016/j.bmcl.2011.08.061

Reference yield:

: 5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazole-3-carboxylic acid ethyl ester

: 1345042-07-0
{3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium hydroxide / tetrahydrofuran; water / 50 - 60 °C

2: oxalyl dichloride / N,N-dimethyl-formamide / 0.33 h / 0 °C

3: hydroxylamine hydrochloride; sodium carbonate / methanol / 6 h / 25 - 30 °C

4: pyridine / 0 - 100 °C / Inert atmosphere

With pyridine; oxalyl dichloride; hydroxylamine hydrochloride; sodium carbonate; ammonium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.08.061

Reference yield:

: 133678-11-2
ethyl 2-oxo-4-(p-chlorophenyl)but-3-enoate

: 1345042-07-0
{3-[5-(4-chlorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazol-3-yl]-[1,2,4]oxadiazol-5-yl}-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: ethanol / 2 h / 25 - 30 °C / Inert atmosphere

1.2: 10 h / Inert atmosphere; Reflux

2.1: ammonium hydroxide / tetrahydrofuran; water / 50 - 60 °C

3.1: oxalyl dichloride / N,N-dimethyl-formamide / 0.33 h / 0 °C

4.1: hydroxylamine hydrochloride; sodium carbonate / methanol / 6 h / 25 - 30 °C

5.1: pyridine / 0 - 100 °C / Inert atmosphere

With pyridine; oxalyl dichloride; hydroxylamine hydrochloride; sodium carbonate; ammonium hydroxide; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.08.061