2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine

Base Information

Chemical Name:2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine
CAS No.:1350880-97-5
Molecular Formula:C₂₄H₂₀F₃N₅O₂S
Molecular Weight:499.516
Hs Code.:

Synonyms:2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine

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Chemical Property of 2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine

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Technology Process of 2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine

There total 6 articles about 2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine 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:

: 1350881-12-7
2-[3-(4-fluorophenyl)-5-(piperidin-3-yl)-1H-pyrazoI-1-yl]pyrimidine

: 60230-36-6
2,6-difluorobenzene-1-sulfonyl chloride

: 1350880-97-5
2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 189442-78-2
(±)-tert-butyl 3-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate

: 1350880-97-5
2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1.1: methylmagnesium bromide / tetrahydrofuran / 1 h / 0 °C

1.2: 20 °C

2.1: hydrazine / ethanol / 3 h / 75 °C

3.1: caesium carbonate; 1,10-Phenanthroline / copper(l) iodide / toluene / 4 h / 120 °C / Inert atmosphere

4.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; 1,10-Phenanthroline; methylmagnesium bromide; caesium carbonate; N-ethyl-N,N-diisopropylamine; hydrazine; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 71381-75-4,88495-54-9,84358-12-3
N-(tert-butyloxycarbonyl)nipecotic acid

: 1350880-97-5
2-[5-{1-[(2,6-difluorophenyl)sulfonyl]piperidin-3-yl}-3-(4-fluorophenyl)-1H-pyrazol-1-yl]pyrimidine

Guidance literature:: Multi-step reaction with 6 steps

1.1: dmap; triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

2.1: methylmagnesium bromide / tetrahydrofuran / 1 h / 0 °C

2.2: 20 °C

3.1: hydrazine / ethanol / 3 h / 75 °C

4.1: caesium carbonate; 1,10-Phenanthroline / copper(l) iodide / toluene / 4 h / 120 °C / Inert atmosphere

5.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 20 °C

6.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; dmap; 1,10-Phenanthroline; methylmagnesium bromide; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; hydrazine; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;