(R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

Base Information

Chemical Name:(R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate
CAS No.:1329170-35-5
Molecular Formula:C₃₂H₄₉N₅O₇Si
Molecular Weight:643.856
Hs Code.:

(R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

Synonyms:(R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

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Chemical Property of (R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

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Technology Process of (R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

There total 6 articles about (R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate 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: 71.0%

: 1329170-34-4
(R)-2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoic acid

: 74-88-4
methyl iodide

: 1329170-35-5
(R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2020.126949

Reference yield:

: 54594-06-8
D-allylglycine

: 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

: 1329170-35-5
(R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; copper(l) iodide / dimethyl sulfoxide / 18 h / 90 °C / Sealed tube; Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C

With copper(l) iodide; potassium carbonate; In dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

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

: 1329170-35-5
(R)-methyl 2-(2-(2-((S)-1-(tert-butoxycarbonylamino)but-3-en-1-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-4-yl)-5-(methoxycarbonylamino)phenylamino)pent-4-enoate

Guidance literature:: Multi-step reaction with 3 steps

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

2: potassium carbonate; copper(l) iodide / dimethyl sulfoxide / 18 h / 90 °C / Inert atmosphere

3: potassium carbonate / N,N-dimethyl-formamide / 20 h / 20 °C

With copper(l) iodide; N-Methyldicyclohexylamine; potassium carbonate; In tetrahydrofuran; dimethyl sulfoxide; N,N-dimethyl-formamide;