5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one

Base Information

Chemical Name:5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one
CAS No.:321721-24-8
Molecular Formula:C₂₂H₂₁BrCl₂N₄O₃S
Molecular Weight:572.31
Hs Code.:

5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1<i>H</i>-imidazo[1,2-<i>a</i>]imidazol-2-one

Synonyms:5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one

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Chemical Property of 5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one

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Technology Process of 5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one

There total 5 articles about 5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-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: 66.5%

: 796872-01-0
(R)-methanesulfonic acid 3-[5-(4-bromobenzyl)-7-(3,5-dichlorophenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-α]imidazolyl-3-sulfonyl]propyl ester

: 321721-24-8
5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one

Guidance literature:: With ammonia; In ethanol; at 80 ℃;
DOI:10.1021/jm049657b

Reference yield:

: 321656-73-9
(R)-3-(4-bromobenzyl)-1-(3,5-dichlorophenyl)-5-iodo-3-methyl-1H-imidazo[1,2-α]imidazol-2-one

: 321721-24-8
5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: cyclopentylmagnesium bromide / tetrahydrofuran / 0.67 h / -40 °C

1.2: SO₂ / tetrahydrofuran / 1.25 h / -40 - 20 °C

1.3: potassium carbonate / dimethylformamide / 70 - 80 °C

2.1: 31 percent / HBr / acetic acid; methanol / 20 °C

3.1: triethylamine / CH₂Cl₂ / 3 h / 20 °C

4.1: 66.5 percent / NH₃ / ethanol / 80 °C

With ammonia; hydrogen bromide; triethylamine; cyclopentylmagnesium bromide; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetic acid;
DOI:10.1021/jm049657b

Reference yield:

: 321656-72-8
(R)-3-(4-bromobenzyl)-1-(3,5-dichlorophenyl)-3-methyl-1-hydroimidazo[1,2-a]imidazol-2-one

: 321721-24-8
5-(3-amino-propane-1-sulfonyl)-3-(4-bromo-benzyl)-1-(3,5-dichloro-phenyl)-3-methyl-1H-imidazo[1,2-a]imidazol-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-iodosuccinimide; pyridinium p-toluenesulfonate / CH₂Cl₂ / 0 °C

2.1: cyclopentylmagnesium bromide / tetrahydrofuran / 0.67 h / -40 °C

2.2: SO₂ / tetrahydrofuran / 1.25 h / -40 - 20 °C

2.3: potassium carbonate / dimethylformamide / 70 - 80 °C

3.1: 31 percent / HBr / acetic acid; methanol / 20 °C

4.1: triethylamine / CH₂Cl₂ / 3 h / 20 °C

5.1: 66.5 percent / NH₃ / ethanol / 80 °C

With N-iodo-succinimide; ammonia; hydrogen bromide; pyridinium p-toluenesulfonate; triethylamine; cyclopentylmagnesium bromide; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetic acid;
DOI:10.1021/jm049657b