1H-imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-[2-(1-methyl-1-fenylethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl

Base Information

Chemical Name:1H-imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-[2-(1-methyl-1-fenylethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl
CAS No.:852357-73-4
Molecular Formula:C₃₃H₃₆N₆O₃
Molecular Weight:564.687
Hs Code.:

Synonyms:1H-imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-[2-(1-methyl-1-fenylethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl

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Chemical Property of 1H-imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-[2-(1-methyl-1-fenylethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl

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Technology Process of 1H-imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-[2-(1-methyl-1-fenylethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl

There total 1 articles about 1H-imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-[2-(1-methyl-1-fenylethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl 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: 77.0%

: 1014987-69-9
5-(1-hydroxy-1-methyl-ethyl)-3-{2'-[2-(1-methyl-1-phenyl-ethyl)-2H-tetrazol-5-yl]-biphenyl-4-yl-methyl}-2-propyl-3H-imidazol-4-carboxylic acid ethyl ester

: 852357-73-4
1H-imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[2'-[2-(1-methyl-1-fenylethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl

Guidance literature:: 5-(1-hydroxy-1-methyl-ethyl)-3-{2'-[2-(1-methyl-1-phenyl-ethyl)-2H-tetrazol-5-yl]-biphenyl-4-yl-methyl}-2-propyl-3H-imidazol-4-carboxylic acid ethyl ester; With sodium hydroxide; water; In tetrahydrofuran; Heating / reflux;

With water; acetic acid; for 0.25h; Product distribution / selectivity;