[4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

Base Information

Chemical Name:[4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester
CAS No.:1329167-41-0
Molecular Formula:C₂₉H₄₅N₅O₇SSi
Molecular Weight:635.857
Hs Code.:

[4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

Synonyms:[4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

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Chemical Property of [4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

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Technology Process of [4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

There total 4 articles about [4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic 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: 58.0%

: 14418-84-9
allylsulfonyl chloride

: 1329167-30-7
tert-butyl N-[(1S)-1-(4-{2-amino-4-[(methoxycarbonyl)-amino]phenyl}-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazol-2-yl)but-3-en-1-yl]carbamate

: 1329167-41-0
[4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃;

Reference yield:

: 76513-69-4
(2-trimethylethylsilylethoxy)methyl chloride

: 1329167-41-0
[4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: N-Methyldicyclohexylamine / tetrahydrofuran / 20 h / 0 - 20 °C

2: potassium carbonate; ammonium hydroxide; L-proline; copper(l) iodide / dimethyl sulfoxide / 20 h / 85 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 °C

With ammonium hydroxide; copper(l) iodide; N-Methyldicyclohexylamine; potassium carbonate; N-ethyl-N,N-diisopropylamine; L-proline; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 1329167-28-3
{3-bromo-4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-3H-imidazol-4-yl]phenyl}carbamic acid methyl ester

: 1329167-41-0
[4-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-3-(prop-2-ene-1-sulfonylamino)phenyl]carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: N-Methyldicyclohexylamine / tetrahydrofuran / 20 h / 0 - 20 °C

2: potassium carbonate; ammonium hydroxide; L-proline; copper(l) iodide / dimethyl sulfoxide / 20 h / 85 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 °C

With ammonium hydroxide; copper(l) iodide; N-Methyldicyclohexylamine; potassium carbonate; N-ethyl-N,N-diisopropylamine; L-proline; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;