(E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide

Base Information

Chemical Name:(E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide
CAS No.:1312711-40-2
Molecular Formula:C₃₁H₂₉F₅N₆O₂
Molecular Weight:612.602
Hs Code.:

Synonyms:(E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide

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Chemical Property of (E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide

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Technology Process of (E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide

There total 5 articles about (E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide 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: 71.0%

: 140-10-3
(E)-3-phenylacrylic acid

: 1312711-11-7
1-(1H-1,2,4-triazol-1-yl)-2-(2,4-difluorophenyl)-3-[4-(4-amino-2-(trifluoromethyl)phenyl)piperazin-1-yl]-propan-2-ol

: 1312711-40-2
(E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/j.ejmech.2011.04.022

Reference yield:

: 381242-61-1
1-[4-nitro-2-(trifluoromethyl)phenyl]piperazine

: 1312711-40-2
(E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / ethanol / 5 h / 70 - 80 °C

2: hydrazine hydrate / ethanol / 3 h / 70 - 80 °C

3: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0 - 20 °C

With dmap; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In ethanol; dichloromethane;
DOI:10.1016/j.ejmech.2011.04.022

Reference yield:

: 777-37-7
4-chloro-3-(trifluoromethyl)nitrobenzene

: 1312711-40-2
(E)-N-(4-(4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)-propyl]-piperazin-1-yl)-3-(trifluoromethyl)-phenyl)-cinnamamide

Guidance literature:: Multi-step reaction with 4 steps

1: acetonitrile / 10 h / Reflux

2: triethylamine / ethanol / 5 h / 70 - 80 °C

3: hydrazine hydrate / ethanol / 3 h / 70 - 80 °C

4: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0 - 20 °C

With dmap; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In ethanol; dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2011.04.022