4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine

Base Information

Chemical Name:4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine
CAS No.:1428253-01-3
Molecular Formula:C₂₀H₂₃F₅N₄
Molecular Weight:414.421
Hs Code.:

Synonyms:4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine

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Chemical Property of 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine

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Technology Process of 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine

There total 4 articles about 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)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: 91.3%

: 1428253-15-9
benzyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine-1-carboxylate

: 1428253-01-3
4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine

Guidance literature:: With palladium 10% on activated carbon; ammonium formate; In methanol; at 20 ℃; for 1h;

Reference yield:

: 1428252-98-5
benzyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1H-imidazol-2-yl)piperidine-1-carboxylate

: 1428253-01-3
4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -20 - 20 °C

1.2: 0.08 h / 20 °C

1.3: 2 h / 100 °C / Microwave irradiation

2.1: toluene-4-sulfonic acid / water; acetone / 168 h / 50 °C

3.1: N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 0.17 h / 20 °C

3.2: 20 °C

4.1: palladium 10% on activated carbon; ammonium formate / methanol / 1 h / 20 °C

With palladium 10% on activated carbon; ammonium formate; sodium hexamethyldisilazane; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water; 1,2-dichloro-ethane; acetone;

Reference yield:

: 1428252-99-6
benzyl 4-(1-((1,3-dioxolan-2-yl)methyl)-4-(4-fluoro-3-(trifluoromethyl)phenyl)-1H-imidazol-2-yl)piperidine-1-carboxylate

: 1428253-01-3
4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-(3-fluoroazetidin-1-yl)ethyl)-1H-imidazol-2-yl)piperidine

Guidance literature:: Multi-step reaction with 3 steps

1.1: toluene-4-sulfonic acid / water; acetone / 168 h / 50 °C

2.1: N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 0.17 h / 20 °C

2.2: 20 °C

3.1: palladium 10% on activated carbon; ammonium formate / methanol / 1 h / 20 °C

With palladium 10% on activated carbon; ammonium formate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In methanol; water; 1,2-dichloro-ethane; acetone;