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

Base Information

Chemical Name:(S)-3-(3-aminophenyl)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)imidazolidin-2-one
CAS No.:1401344-81-7
Molecular Formula:C₂₆H₂₇N₅O₂
Molecular Weight:441.533
Hs Code.:

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

Suppliers and Price of (S)-3-(3-aminophenyl)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)imidazolidin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

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

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

There total 7 articles about (S)-3-(3-aminophenyl)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)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: 89.0%

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

: 1401344-81-7
(S)-3-(3-aminophenyl)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)imidazolidin-2-one

Guidance literature:: With 5% Pd/C; acetic acid; In ethanol; toluene; for 3h; Inert atmosphere;
DOI:10.1039/c2cc34791a

Reference yield:

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

: 1401344-81-7
(S)-3-(3-aminophenyl)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)imidazolidin-2-one

Guidance literature:: Multi-step reaction with 10 steps

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

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

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

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

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

6: sodium hydrogencarbonate / dichloromethane; water / Inert atmosphere

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

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

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

10: acetic acid; 5% Pd/C / ethanol; toluene / 3 h / Inert atmosphere

With 1H-imidazole; dmap; di-isopropyl azodicarboxylate; 5% Pd/C; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; acetic acid; triphenylphosphine; urea; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;
DOI:10.1039/c2cc34791a

Reference yield:

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

: 1401344-81-7
(S)-3-(3-aminophenyl)-4-methyl-1-(3-((S)-5-methyl-2-oxo-3-phenylimidazolidin-1-yl)phenyl)imidazolidin-2-one

Guidance literature:: Multi-step reaction with 7 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

7: acetic acid; 5% Pd/C / ethanol; toluene / 3 h / Inert atmosphere

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