(4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one

Base Information

Chemical Name:(4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one
CAS No.:1276021-58-9
Molecular Formula:C₁₉H₂₂N₂O₃
Molecular Weight:326.395
Hs Code.:

Synonyms:(4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one

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Chemical Property of (4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one

Chemical Property:

Purity/Quality:

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Technology Process of (4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one

There total 7 articles about (4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-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:

: 1276021-57-8
(1S,2R)-N₂-(4-methoxybenzyl)-1-(4-methoxyphenyl)propane-1,2-diamine

: 530-62-1
1,1'-carbonyldiimidazole

: 1276021-58-9
(4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one

Guidance literature:: With triethylamine; In dichloromethane; for 1h; Reflux;

Reference yield:

: 4180-23-8,25086-72-0,63589-56-0
E-1-(4'-methoxyphenyl)prop-1-ene

: 1276021-58-9
(4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydroxide / water; propan-1-ol / 0.08 h / 20 °C

1.2: 0.17 h / 20 °C

1.3: 0 °C

2.1: triethylamine / dichloromethane / 18 h / 0 - 20 °C

3.1: sodium azide / N,N-dimethyl-formamide / 2 h / 70 °C

4.1: hydrogen / palladium 10% on activated carbon / ethanol / 24 h / 20 °C / 3000.3 Torr / Inert atmosphere

5.1: ethanol / 4 h / 20 °C

5.2: 14 h / 0 - 20 °C

6.1: trifluoroacetic acid / dichloromethane / 20 °C

7.1: triethylamine / dichloromethane / 1 h / Reflux

With sodium azide; hydrogen; triethylamine; trifluoroacetic acid; sodium hydroxide; palladium 10% on activated carbon; In propan-1-ol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1276021-53-4
tert-butyl (1S,2S)-2-hydroxy-1-(4-methoxyphenyl)propylcarbamate

: 1276021-58-9
(4S,5R)-1-(4-methoxybenzyl)-4-(4-methoxyphenyl)-5-methylimidazolidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 18 h / 0 - 20 °C

2.1: sodium azide / N,N-dimethyl-formamide / 2 h / 70 °C

3.1: hydrogen / palladium 10% on activated carbon / ethanol / 24 h / 20 °C / 3000.3 Torr / Inert atmosphere

4.1: ethanol / 4 h / 20 °C

4.2: 14 h / 0 - 20 °C

5.1: trifluoroacetic acid / dichloromethane / 20 °C

6.1: triethylamine / dichloromethane / 1 h / Reflux

With sodium azide; hydrogen; triethylamine; trifluoroacetic acid; palladium 10% on activated carbon; In ethanol; dichloromethane; N,N-dimethyl-formamide;