(E)-N-(4-{4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propyl]piperazin-1-yl}-3-fluorophenyl)-3-(2-fluorophenyl)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-fluorophenyl)-3-(2-fluorophenyl)cinnamamide
CAS No.:1268242-65-4
Molecular Formula:C₃₀H₂₈F₄N₆O₂
Molecular Weight:580.585
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-fluorophenyl)-3-(2-fluorophenyl)cinnamamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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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-fluorophenyl)-3-(2-fluorophenyl)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-fluorophenyl)-3-(2-fluorophenyl)cinnamamide

There total 1 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-fluorophenyl)-3-(2-fluorophenyl)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:

: 950821-44-0
2-(2,4-difluorophenyl)-1-[4-(2-fluoro-4-amino-phenyl)-piperazin-1-yl]-3-(1H-1,2,4-triazol-1-yl)-propan-2-ol

: 18944-77-9
2-fluorocinnamic acid

: 1268242-65-4
(E)-N-(4-{4-[2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propyl]piperazin-1-yl}-3-fluorophenyl)-3-(2-fluorophenyl)cinnamamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 ℃; for 8h;
DOI:10.1016/j.bmcl.2010.12.006