(Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

Base Information

Chemical Name:(Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester
CAS No.:205063-90-7
Molecular Formula:C₃₁H₄₂N₂O₈Si
Molecular Weight:598.769
Hs Code.:

(Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

Synonyms:(Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

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Chemical Property of (Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

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Technology Process of (Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

There total 4 articles about (Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl 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: 72.0%

: 130247-01-7
methyl 2-({[2-(trimethylsilyl)ethoxy]carbonyl}amino)acrylate

: 129150-58-9
benzyl Boc-4-iodophenylalanine

: 205063-90-7
(Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

Guidance literature:: With palladium diacetate; tetrabutyl-ammonium chloride; sodium hydrogencarbonate; hydroquinone; In N,N-dimethyl-formamide; at 85 - 90 ℃; for 18h;
DOI:10.1016/S0957-4166(98)00014-7

Reference yield:

: 103882-09-3,62129-44-6
N-Boc-4-I-Phe-OH

: 205063-90-7
(Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: dimethylformamide / 8 h / 60 °C

2: 72 percent / Pd(OAc)2, Bu₄NCl, NaHCO₃, hydroquinone / dimethylformamide / 18 h / 85 - 90 °C

With palladium diacetate; tetrabutyl-ammonium chloride; sodium hydrogencarbonate; hydroquinone; In N,N-dimethyl-formamide;
DOI:10.1016/S0957-4166(98)00014-7

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 205063-90-7
(Z)-3-[4-((S)-2-Benzyloxycarbonyl-2-tert-butoxycarbonylamino-ethyl)-phenyl]-2-(2-trimethylsilanyl-ethoxycarbonylamino)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: KHCO₃ / dioxane; H₂O / Ambient temperature

2: dimethylformamide / 8 h / 60 °C

3: 72 percent / Pd(OAc)2, Bu₄NCl, NaHCO₃, hydroquinone / dimethylformamide / 18 h / 85 - 90 °C

With palladium diacetate; tetrabutyl-ammonium chloride; sodium hydrogencarbonate; potassium hydrogencarbonate; hydroquinone; In 1,4-dioxane; water; N,N-dimethyl-formamide;
DOI:10.1016/S0957-4166(98)00014-7