(S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one

Base Information

Chemical Name:(S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one
CAS No.:1401344-80-6
Molecular Formula:C₂₆H₂₅N₅O₄
Molecular Weight:471.516
Hs Code.:

Synonyms:(S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one

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Chemical Property of (S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one

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Technology Process of (S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one

There total 7 articles about (S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one 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%

: 1401344-79-3
1-((S)-1-hydroxypropan-2-yl)-3-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-1-(3-nitrophenyl)urea

: 1401344-80-6
(S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; urea; In tetrahydrofuran; at 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1039/c2cc34791a

Reference yield:

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

: 1401344-80-6
(S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

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

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

3: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 20 °C

4: di-isopropyl azodicarboxylate; triphenylphosphine; urea / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

With 1H-imidazole; dmap; di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; acetic acid; triphenylphosphine; urea; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c2cc34791a

Reference yield:

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

: 1401344-80-6
(S)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)-3-(3-nitrophenyl)imidazolidin-2-one

Guidance literature:: Multi-step reaction with 6 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

5: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 20 °C

6: di-isopropyl azodicarboxylate; triphenylphosphine; urea / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

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