2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid

Base Information

Chemical Name:2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid
CAS No.:1329167-73-8
Molecular Formula:C₂₇H₄₀N₄O₇Si
Molecular Weight:560.723
Hs Code.:

Synonyms:2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid

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Chemical Property of 2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid

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Technology Process of 2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid

There total 3 articles about 2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic 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:

: 124-38-9,18923-20-1
carbon dioxide

: 1329167-29-4
tert-butyl N-[(1S)-1-(4-{2-bromo-4-[(methoxycarbonyl)-amino]phenyl}-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazol-2-yl)but-3-en-1-yl]carbamate

: 1329167-73-8
2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid

Guidance literature:: tert-butyl N-[(1S)-1-(4-{2-bromo-4-[(methoxycarbonyl)-amino]phenyl}-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-imidazol-2-yl)but-3-en-1-yl]carbamate; With methyllithium; In tetrahydrofuran; at -78 ℃; for 0.5h; Inert atmosphere;

With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.5h;

carbon dioxide; at -78 ℃; for 0.5h;

Reference yield:

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

: 1329167-73-8
2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

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

2.1: methyllithium / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

2.2: 0.5 h / -78 °C

2.3: 0.5 h / -78 °C

With N-Methyldicyclohexylamine; methyllithium; In tetrahydrofuran;

Reference yield:

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

: 1329167-73-8
2-[2-((S)-1-tert-butoxycarbonylaminobut-3-enyl)-1-(2-trimethylsilanylethoxymethyl)-1H-imidazol-4-yl]-5-methoxycarbonylamino-benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

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

2.1: methyllithium / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

2.2: 0.5 h / -78 °C

2.3: 0.5 h / -78 °C

With N-Methyldicyclohexylamine; methyllithium; In tetrahydrofuran;