4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide

Base Information

Chemical Name:4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide
CAS No.:1360627-29-7
Molecular Formula:C₃₃H₃₈Cl₂N₄O₄
Molecular Weight:625.595
Hs Code.:

Synonyms:4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide

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Chemical Property of 4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide

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Technology Process of 4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide

There total 8 articles about 4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide 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: 76.0%

: 1360627-19-5
(2S)-2-(4,5-bis(4-chlorophenyl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydro-1H-imidazole-1-carboxamido)propanoic acid

: 109-89-7
diethylamine

: 1360627-29-7
4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide

Guidance literature:: (2S)-2-(4,5-bis(4-chlorophenyl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydro-1H-imidazole-1-carboxamido)propanoic acid; With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In dichloromethane; for 0.5h; Inert atmosphere;

diethylamine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1016/j.bmc.2012.01.003

Reference yield:

: 673-22-3
2-Hydroxy-4-methoxybenzaldehyde

: 1360627-29-7
4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / acetone / 5 h / 40 °C

2.1: N-Bromosuccinimide / dichloromethane / 24 h / 20 °C

3.1: triethylamine / dichloromethane / 0.5 h / 0 °C

3.2: 0.25 h / 20 °C

4.1: hydrogenchloride; water / 1 h / 110 °C

4.2: 20 °C

5.1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / dichloromethane / 0.5 h / Inert atmosphere

5.2: 3 h / 20 °C

With hydrogenchloride; N-Bromosuccinimide; water; potassium carbonate; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In dichloromethane; acetone;
DOI:10.1016/j.bmc.2012.01.003

Reference yield:

: 115294-32-1,120375-16-8
4-chloro-benzoic acid-[erythro-4,4'-dichloro-α'-(4-chloro-benzylidenamino)-bibenzyl-α-ylamide]

: 1360627-29-7
4,5-bis(4-chlorophenyl)-N-((S)-1-(diethylamino)-1-oxopropan-2-yl)-2-(2-isopropoxy-4-methoxyphenyl)-4,5-dihydroimidazole-1-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sulfuric acid / 3 h / 120 °C

2.1: N-Bromosuccinimide / dichloromethane / 24 h / 20 °C

3.1: triethylamine / dichloromethane / 0.5 h / 0 °C

3.2: 0.25 h / 20 °C

4.1: hydrogenchloride; water / 1 h / 110 °C

4.2: 20 °C

5.1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / dichloromethane / 0.5 h / Inert atmosphere

5.2: 3 h / 20 °C

With hydrogenchloride; N-Bromosuccinimide; sulfuric acid; water; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1016/j.bmc.2012.01.003