1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

Base Information

Chemical Name:1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea
CAS No.:1401344-78-2
Molecular Formula:C₃₂H₄₁N₅O₅Si
Molecular Weight:603.794
Hs Code.:

Synonyms:1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

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Chemical Property of 1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

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Technology Process of 1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

There total 8 articles about 1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea 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: 39.0%

: 1401344-77-1
(S)-3-(3-isocyanatophenyl)-4-methyl-1-phenylimidazolidin-2-one

: 1401344-71-5
N-(1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-nitroaniline

: 1401344-78-2
1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; for 48h; Inert atmosphere;
DOI:10.1039/c2cc34791a

Reference yield:

: 1401344-70-4
(S)-2-((3-nitrophenyl)amino)propan-1-ol

: 1401344-78-2
1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; 1H-imidazole / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

2: dmap / dichloromethane / 48 h / 20 °C / Inert atmosphere

With 1H-imidazole; dmap; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c2cc34791a

Reference yield:

: (S)-1-(1-hydroxypropan-2-yl)-1-(3-nitrophenyl)-3-phenylurea

: 1401344-78-2
1-((S)-1-((tert-butyldimethylsilyl)oxy)propan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine; urea / tetrahydrofuran / 0.5 h / 20 °C

2: 5% Pd/C / ethanol / Inert atmosphere

3: sodium hydrogencarbonate / dichloromethane; water / Inert atmosphere

4: dmap / dichloromethane / 48 h / 20 °C / Inert atmosphere

With dmap; di-isopropyl azodicarboxylate; 5% Pd/C; sodium hydrogencarbonate; triphenylphosphine; urea; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1039/c2cc34791a