N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide

Base Information

Chemical Name:N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide
CAS No.:1448682-55-0
Molecular Formula:C₁₉H₂₉F₃N₂O₂S
Molecular Weight:406.513
Hs Code.:

Synonyms:N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide

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Chemical Property of N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide

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Technology Process of N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide

There total 6 articles about N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide 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: 61.9%

: 69682-13-9
4-(tert-butyl)piperidine hydrochloride

: 1448682-02-7
N-[(1S)-2,2,2-trifluoro-1-(4-formylphenyl)ethyl]methanesulfonamide

: 1448682-55-0
N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; triethylamine; In dichloromethane; at 22 ℃; for 15h;

Reference yield:

: 1448682-01-6
N-[(1S)-1-(4-bromophenyl)-2,2,2-trifluoro-ethyl]methanesulfonamide

: 1448682-55-0
N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: palladium diacetate; catacxium A; N,N,N,N,-tetramethylethylenediamine; hydrogen / toluene / 16 h / 95 °C / 3878.71 Torr

2: sodium tris(acetoxy)borohydride; acetic acid; triethylamine / dichloromethane / 15 h / 22 °C

With N,N,N,N,-tetramethylethylenediamine; hydrogen; palladium diacetate; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; catacxium A; In dichloromethane; toluene;

Reference yield:

: 1122-91-4
4-bromo-benzaldehyde

: 1448682-55-0
N-[(1S)-1-{4-[(4-tert-butylpiperidin-1-yl)methyl]phenyl}-2,2,2-trifluoroethyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1: sodium hydroxide / toluene / 12 h / 20 °C

2: tetrabutylammonium acetate / N,N-dimethyl-formamide / 1.5 h / 0 - 5 °C

3: hydrogenchloride / 1,4-dioxane; methanol / 1 h / 20 °C

4: dmap; 2,6-dimethylpyridine / dichloromethane / 20 h / 0 - 20 °C

5: palladium diacetate; catacxium A; N,N,N,N,-tetramethylethylenediamine; hydrogen / toluene / 16 h / 95 °C / 3878.71 Torr

6: sodium tris(acetoxy)borohydride; acetic acid; triethylamine / dichloromethane / 15 h / 22 °C

With 2,6-dimethylpyridine; hydrogenchloride; dmap; N,N,N,N,-tetramethylethylenediamine; hydrogen; tetrabutylammonium acetate; palladium diacetate; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; sodium hydroxide; catacxium A; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; toluene;