(S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid

Base Information

Chemical Name:(S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid
CAS No.:374803-66-4
Molecular Formula:C₃₅H₃₉NO₆Si
Molecular Weight:597.783
Hs Code.:

Synonyms:(S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid

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Chemical Property of (S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid

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Technology Process of (S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid

There total 5 articles about (S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid 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: 50.0%

: 16652-64-5
O-benzyl-S-tyrosine

: 374803-65-3
{2-bromo-5-[2-(trimethylsilyl)ethoxymethoxy]phenyl}(phenyl)methanone

: 374803-66-4
(S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid

Guidance literature:: With copper(l) iodide; potassium carbonate; In N,N-dimethyl-formamide; at 90 ℃; for 72h;
DOI:10.1016/S0040-4020(01)00743-8

Reference yield:

: 60080-98-0
(2-bromo-5-methoxyphenyl)(phenyl)methanone

: 374803-66-4
(S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: BCl₃; nBu₄NI / CH₂Cl₂ / 14 h / -78 - 25 °C

2: 11.3 g / iPr₂NEt / CH₂Cl₂ / 18 h / 25 °C

3: 50 percent / K₂CO₃; CuI / dimethylformamide / 72 h / 90 °C

With copper(l) iodide; boron trichloride; tetra-(n-butyl)ammonium iodide; potassium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)00743-8

Reference yield:

: 35450-36-3
methyl 2-bromo-5-methoxybenzoate

: 374803-66-4
(S)-2-[2-Benzoyl-4-(2-trimethylsilanyl-ethoxymethoxy)-phenylamino]-3-(4-benzyloxy-phenyl)-propionic acid

Guidance literature:: Multi-step reaction with 5 steps

1: PhMgCl / tetrahydrofuran / 1 h / -5 °C

2: 37.4 g / tetrahydrofuran / 5 h / -10 - 25 °C

3: BCl₃; nBu₄NI / CH₂Cl₂ / 14 h / -78 - 25 °C

4: 11.3 g / iPr₂NEt / CH₂Cl₂ / 18 h / 25 °C

5: 50 percent / K₂CO₃; CuI / dimethylformamide / 72 h / 90 °C

With copper(l) iodide; phenylmagnesium chloride; boron trichloride; tetra-(n-butyl)ammonium iodide; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)00743-8