tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate
CAS No.:1082950-60-4
Molecular Formula:C₂₁H₂₅F₄N₃O₂
Molecular Weight:427.442
Hs Code.:

Synonyms:tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

There total 9 articles about tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate 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: 86.0%

: 1082950-48-8
tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1H-imidazol-2-yl)piperidine-1-carboxylate

: 74-88-4
methyl iodide

: 1082950-60-4
tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

Guidance literature:: With potassium hydroxide; In dimethyl sulfoxide; at 25 - 30 ℃;
DOI:10.1021/op200351g

Reference yield: 75.3%

: 1370337-77-1
tert-butyl 4-((2-(4-fluoro-3-(trifluoromethyl)phenyl)-2-oxoethyl)(methyl)carbamoyl)piperidine-1-carboxylate

: 1082950-60-4
tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

Guidance literature:: With ammonium acetate; acetic acid; In methanol; at 140 ℃; Inert atmosphere; Large scale reaction;
DOI:10.1021/op200351g

Reference yield:

: 1370337-76-0
1-(4-fluoro-3-(trifluoromethyl)phenyl)-2-(methylamino)ethanone hydrochloride

: 1082950-60-4
tert-butyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 4-methyl-morpholine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / tetrahydrofuran; ethyl acetate / 0.42 h / 0 - 5 °C

2: ammonium acetate; acetic acid / ethanol

With 4-methyl-morpholine; ammonium acetate; acetic acid; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; In tetrahydrofuran; ethanol; ethyl acetate;
DOI:10.1021/op200351g