N-[(2S,3R)-4-(4-chlorophenyl)-3-(3-cyanophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-yl]-2-methyl-2-[5-(trifluoromethyl)pyridin-2-yloxy]propanamide

Base Information

Chemical Name:N-[(2S,3R)-4-(4-chlorophenyl)-3-(3-cyanophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-yl]-2-methyl-2-[5-(trifluoromethyl)pyridin-2-yloxy]propanamide
CAS No.:1092698-93-5
Molecular Formula:C₂₉H₂₆ClF₃N₆O₂
Molecular Weight:583.013
Hs Code.:

Synonyms:N-[(2S,3R)-4-(4-chlorophenyl)-3-(3-cyanophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-yl]-2-methyl-2-[5-(trifluoromethyl)pyridin-2-yloxy]propanamide

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Chemical Property of N-[(2S,3R)-4-(4-chlorophenyl)-3-(3-cyanophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-yl]-2-methyl-2-[5-(trifluoromethyl)pyridin-2-yloxy]propanamide

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Technology Process of N-[(2S,3R)-4-(4-chlorophenyl)-3-(3-cyanophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-yl]-2-methyl-2-[5-(trifluoromethyl)pyridin-2-yloxy]propanamide

There total 1 articles about N-[(2S,3R)-4-(4-chlorophenyl)-3-(3-cyanophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-yl]-2-methyl-2-[5-(trifluoromethyl)pyridin-2-yloxy]propanamide 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: 63.0%

: 605680-62-4
2-methyl-2-{[5-(trifluoromethyl)pyridin-2-yl]oxy}propanoic acid

: 1092698-92-4
3-[(2S,3R)-3-amino-1-(4-chlorophenyl)-4-(1H-1,2,4-triazol-1-yl)butan-2-yl]benzonitrile

: 1092698-93-5
N-[(2S,3R)-4-(4-chlorophenyl)-3-(3-cyanophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-yl]-2-methyl-2-[5-(trifluoromethyl)pyridin-2-yloxy]propanamide

Guidance literature:: With 1,3,5-trichloro-2,4,6-triazine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In acetonitrile; at 20 ℃;
DOI:10.1016/j.tet.2008.09.057