N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide

Base Information

Chemical Name:N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide
CAS No.:1349807-51-7
Molecular Formula:C₂₄H₂₂N₄O₆S
Molecular Weight:494.528
Hs Code.:

Synonyms:N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide

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Chemical Property of N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide

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Technology Process of N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide

There total 5 articles about N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide 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: 49.8%

: 1349808-14-5
1-(4-amino-3-methylphenylsulfonyl)-5-methyl-4-phenylimidazolidin-2-one

: 122-04-3
4-nitro-benzoyl chloride

: 1349807-51-7
N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃;
DOI:10.1016/j.bmcl.2011.09.025

Reference yield:

: 1349808-06-5
2,2,2-trifluoro-N-(4-(2-methoxy-5-methyl-4-phenyl-4,5-dihydroimidazol-1-ylsulfonyl)-2-methylphenyl)acetamide

: 1349807-51-7
N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / ethanol / 0 °C

2: hydrogenchloride / diethyl ether / 3 h / 20 °C

3: pyridine / dichloromethane / 20 °C

With pyridine; hydrogenchloride; sodium hydroxide; In diethyl ether; ethanol; dichloromethane;
DOI:10.1016/j.bmcl.2011.09.025

Reference yield:

: 1349808-34-9
C₁₁H₁₄N₂O

: 1349807-51-7
N-(2-methyl-4-((4S)-5-methyl-2-oxo-4-phenylimidazolidin-1-ylsulfonyl)phenyl)-4-nitrobenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydrogencarbonate / water; acetone

2: sodium hydroxide / ethanol / 0 °C

3: hydrogenchloride / diethyl ether / 3 h / 20 °C

4: pyridine / dichloromethane / 20 °C

With pyridine; hydrogenchloride; sodium hydrogencarbonate; sodium hydroxide; In diethyl ether; ethanol; dichloromethane; water; acetone;
DOI:10.1016/j.bmcl.2011.09.025