4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester

Base Information

Chemical Name:4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester
CAS No.:1073543-67-5
Molecular Formula:C₃₅H₄₆ClN₃O₄S
Molecular Weight:640.287
Hs Code.:

4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester

Synonyms:4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester

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Chemical Property of 4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester

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Technology Process of 4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester

There total 1 articles about 4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester 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:

: 632333-34-7
(S)-2-acetylsulfanylmethyl-4-methylpentanoic acid

: 1073543-62-0
4’-(5-aminomethyl-2-butyl-4-chloroimidazol-1-ylmethyl)biphenyl-2-carboxylic acid t-butyl ester

: 1073543-67-5
4'-5-[((S)-2-acetylsulfanylmethyl-4-methylpentanoylamino)methyl]-2-butyl-4-chloroimidazol-1-ylmethylbiphenyl-2-carboxylic acid t-butyl ester

Guidance literature:: (S)-2-acetylsulfanylmethyl-4-methylpentanoic acid; With HATU; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 1h;

4’-(5-aminomethyl-2-butyl-4-chloroimidazol-1-ylmethyl)biphenyl-2-carboxylic acid t-butyl ester; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 4h;