ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate

Base Information

Chemical Name:ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate
CAS No.:1352428-24-0
Molecular Formula:C₁₉H₁₆N₄O₆
Molecular Weight:396.359
Hs Code.:

Synonyms:ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate

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Chemical Property of ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate

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Technology Process of ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate

There total 3 articles about ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate 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:

: C₂₁H₂₂N₄O₇

: 1352428-24-0
ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate

Guidance literature:: With sodium hydroxide; In ethanol; water; toluene; at 20 ℃; for 48h;
DOI:10.1016/j.tet.2011.11.013

Reference yield:

: 1352428-12-6
diethyl 1-(1-(dimethylamino)-3-oxo-3-phenylprop-1-en-2-yl)hydrazine-1,2-dicarboxylate

: 1352428-24-0
ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / ethanol; water; toluene / 24 h / 20 °C

2: sodium hydroxide / ethanol; water; toluene / 48 h / 20 °C

With hydrogenchloride; sodium hydroxide; In ethanol; water; toluene;
DOI:10.1016/j.tet.2011.11.013

Reference yield:

: 1131-80-2,1201-93-0,31919-75-2
(E)-3-(N,N-dimethylamino)-1-phenyl-2-propen-1-one

: 1352428-24-0
ethyl (5-benzoyl-3-(4-nitrophenyl)-2-oxo-2,3-dihydro-1H-imidazol-1-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: toluene; acetonitrile / 24 h / 20 °C

2: hydrogenchloride / ethanol; water; toluene / 24 h / 20 °C

3: sodium hydroxide / ethanol; water; toluene / 48 h / 20 °C

With hydrogenchloride; sodium hydroxide; In ethanol; water; toluene; acetonitrile; 1: Michael addition;
DOI:10.1016/j.tet.2011.11.013