Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

Base Information

Chemical Name:Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester
CAS No.:182176-21-2
Molecular Formula:C₃₅H₄₁N₃O₅
Molecular Weight:583.728
Hs Code.:

Synonyms:Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

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Chemical Property of Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

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Technology Process of Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

There total 3 articles about Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-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:

: 17186-53-7,92698-80-1
L-phenylalanine cyclohexylamide

: 182176-21-2
Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / Et(i-Pr)2N / various solvent(s) / 30 h / 100 °C / in N-methylpyrrolidin-2-one (NMP)

2: 1.) 2 N HCl 2.) Et(i-Pr)2N / 1.) dioxane, r.t., 3 h; 2.) NMP, r.t., 2.5 h

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In various solvent(s);
DOI:10.1002/hlca.19960790508

Reference yield:

: 182176-14-3
rac-4-(iodomethyl)-4-isopropyl-2-phenyloxazol-5(4H)-one

: 182176-21-2
Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / Et(i-Pr)2N / various solvent(s) / 30 h / 100 °C / in N-methylpyrrolidin-2-one (NMP)

2: 1.) 2 N HCl 2.) Et(i-Pr)2N / 1.) dioxane, r.t., 3 h; 2.) NMP, r.t., 2.5 h

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In various solvent(s);
DOI:10.1002/hlca.19960790508

Reference yield:

: 98-88-4
benzoyl chloride

: 4-Isopropyl-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid ((S)-1-cyclohexylcarbamoyl-2-phenyl-ethyl)-amide

: 182176-22-3
Benzoic acid (S)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

: 182176-21-2
Benzoic acid (R)-2-benzoylamino-2-((S)-1-cyclohexylcarbamoyl-2-phenyl-ethylcarbamoyl)-3-methyl-butyl ester

Guidance literature:: With hydrogenchloride; N-ethyl-N,N-diisopropylamine; Yield given. Multistep reaction. Yields of byproduct given; 1.) dioxane, r.t., 3 h; 2.) NMP, r.t., 2.5 h;
DOI:10.1002/hlca.19960790508