1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

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Chemical Name:1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine
CAS No.:1227159-14-9
Molecular Formula:C₂₉H₃₀F₃N₇O
Molecular Weight:549.599
Hs Code.:

Synonyms:1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

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Chemical Property of 1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

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Technology Process of 1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

There total 4 articles about 1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine 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: 42.0%

: 27374-25-0
[(1-Ethoxycyclopropyl)oxy]trimethylsilane

: 1227159-13-8
1-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

: 1227159-14-9
1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

Guidance literature:: [(1-Ethoxycyclopropyl)oxy]trimethylsilane; 1-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine; With acetic acid; In methanol; at 20 ℃; for 0.166667h; Inert atmosphere; Molecular sieve;

With sodium cyanoborohydride; In methanol; for 2h; Reflux;

Reference yield:

: 101990-73-2
2-chloro-pyridin-4-ylmethyl chloride

: 1227159-14-9
1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium tert-butylate / tetrahydrofuran / Reflux

2.1: water; ethyl acetate / 150 °C / Inert atmosphere

3.1: acetic acid / methanol / 0.17 h / 20 °C / Inert atmosphere; Molecular sieve

3.2: 2 h / Reflux

With potassium tert-butylate; acetic acid; In tetrahydrofuran; methanol; water; ethyl acetate;

Reference yield:

: 100704-10-7
(2-chloropyridin-4-yl)methanol

: 1227159-14-9
1-cyclopropyl-4-(4-{[5-methyl-3-(3-{4-[1-(trifluoromethyl)cyclopropyl]phenyl}-1,2,4-oxadiazol-5-yl)-1H-pyrazol-1-yl]methyl}pyridin-2-yl)piperazine

Guidance literature:: Multi-step reaction with 4 steps

1.1: thionyl chloride / dichloromethane / 20 °C

2.1: potassium tert-butylate / tetrahydrofuran / Reflux

3.1: water; ethyl acetate / 150 °C / Inert atmosphere

4.1: acetic acid / methanol / 0.17 h / 20 °C / Inert atmosphere; Molecular sieve

4.2: 2 h / Reflux

With thionyl chloride; potassium tert-butylate; acetic acid; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate;