N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea

Base Information

Chemical Name:N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea
CAS No.:1383480-12-3
Molecular Formula:C₂₈H₃₀F₃N₇O
Molecular Weight:537.588
Hs Code.:

Synonyms:N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea

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Chemical Property of N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea

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Technology Process of N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea

There total 10 articles about N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea 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:

: N-{3-[5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-1H-benzimidazol-1-yl]phenyl}-N'-(2,2,2-trifluoroethyl)urea hydrochloride

: 1489-69-6
Cyclopropanecarboxaldehyde

: 1383480-12-3
N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea

Guidance literature:: N-{3-[5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-1H-benzimidazol-1-yl]phenyl}-N'-(2,2,2-trifluoroethyl)urea hydrochloride; Cyclopropanecarboxaldehyde; With triethylamine; In ethanol; 1,2-dichloro-ethane; at 20 ℃; for 1h;

With sodium tris(acetoxy)borohydride; In ethanol; 1,2-dichloro-ethane; at 20 ℃;

Reference yield:

: 364-73-8
4-Bromo-1-fluoro-2-nitrobenzene

: 1383480-12-3
N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea

Guidance literature:: Multi-step reaction with 7 steps

1.1: 1-methyl-pyrrolidin-2-one / 150 °C

2.1: ethanol; tin(ll) chloride / 100 °C

3.1: hydrogenchloride / water / 150 °C

3.2: 2 h / 100 °C

4.1: dmap; triethylamine / tetrahydrofuran / 1 h / 20 °C

4.2: 20 °C

5.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 120 °C / Inert atmosphere

6.1: hydrogenchloride / ethyl acetate; 1,4-dioxane / 2 h / 20 °C

7.1: triethylamine / ethanol; 1,2-dichloro-ethane / 1 h / 20 °C

7.2: 20 °C

With hydrogenchloride; dmap; ethanol; sodium carbonate; triethylamine; tin(ll) chloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethanol; water; ethyl acetate; 1,2-dichloro-ethane; 5.1: Suzuki Coupling;

Reference yield:

: 877399-74-1
tert-butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate

: 1383480-12-3
N-[3-(5-{1-[1-(Cyclopropylmethyl)piperidin-4-yl]-1H-pyrazol-4-yl}-1H-benzimidazol-1-yl)phenyl]-N'-(2,2,2-trifluoroethyl)urea

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 120 °C / Inert atmosphere

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

3.1: triethylamine / ethanol; 1,2-dichloro-ethane / 1 h / 20 °C

3.2: 20 °C

With hydrogenchloride; sodium carbonate; triethylamine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; ethanol; water; ethyl acetate; 1,2-dichloro-ethane; 1.1: Suzuki Coupling;