4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine

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Chemical Name:4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine
CAS No.:1018325-29-5
Molecular Formula:C₂₀H₂₃Cl₃F₃N₃O
Molecular Weight:484.776
Hs Code.:

Synonyms:4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine

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Chemical Property of 4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine

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Technology Process of 4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine

There total 6 articles about 4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine 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: 17.89%

: 235106-12-4
4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazole

: C₂₂H₂₇Cl₂NO₄S

: 1018325-29-5
4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 - 90 ℃; for 0.833333h;

Reference yield:

: 141060-29-9
tert-butyl 4-(1-ethoxy-1-oxopropan-2-yl)piperidine-1-carboxylate

: 1018325-29-5
4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

1.2: pH 9

2.1: 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 14 h / 112 °C

3.1: N-chloro-succinimide; acetic acid / water / 20 °C

3.2: pH 9

4.1: diisobutylaluminium hydride / tetrahydrofuran / 2.5 h / -10 - 20 °C

4.2: 20 °C / pH 6

5.1: pyridine / dichloromethane / 12.25 h / 0 - 20 °C

6.1: caesium carbonate / N,N-dimethyl-formamide / 0.83 h / 20 - 90 °C

With pyridine; hydrogenchloride; N-chloro-succinimide; diisobutylaluminium hydride; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; acetic acid; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 473837-03-5
tert-butyl 4-(1-ethoxy-1-oxopropan-2-ylidene)piperidine-1-carboxylate

: 1018325-29-5
4-(1-(4-chloro-5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)propan-2-yl)-1-(2,4-dichloro-5-methoxyphenyl)piperidine

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogen / platinum(IV) oxide / ethanol / 14 h

2.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

2.2: pH 9

3.1: 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 14 h / 112 °C

4.1: N-chloro-succinimide; acetic acid / water / 20 °C

4.2: pH 9

5.1: diisobutylaluminium hydride / tetrahydrofuran / 2.5 h / -10 - 20 °C

5.2: 20 °C / pH 6

6.1: pyridine / dichloromethane / 12.25 h / 0 - 20 °C

7.1: caesium carbonate / N,N-dimethyl-formamide / 0.83 h / 20 - 90 °C

With pyridine; hydrogenchloride; N-chloro-succinimide; hydrogen; diisobutylaluminium hydride; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; acetic acid; sodium t-butanolate; platinum(IV) oxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;