8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one

Base Information

Chemical Name:8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one
CAS No.:1620583-22-3
Molecular Formula:C₂₂H₂₁BrCl₂N₄O
Molecular Weight:508.245
Hs Code.:

Synonyms:8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one

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Chemical Property of 8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one

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Technology Process of 8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one

There total 8 articles about 8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-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: 42.0%

: 1448869-75-7
2-bromo-5-((4-chloro-2-methylphenyl)(5-chloro-2-methylphenylamino)methyl)-1-isopropyl-1H-imidazole-4-carboxylic acid

: 1620583-22-3
8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one

Guidance literature:: With diphenyl phosphoryl azide; triethylamine; In 1,2-dimethoxyethane; at 85 ℃; for 2h;

Reference yield:

: 40137-29-9
2-methyl-4-chlorobenzaldehyde

: 1620583-22-3
8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 1.5 h / -78 °C

1.2: 1 h / -73 °C

2.1: triethylamine / dichloromethane / 16 h / 20 °C

3.1: triethylamine / dichloromethane / 19 h / 4 - 20 °C

4.1: lithium hydroxide monohydrate; water / 1,4-dioxane / 40 h / 20 °C

5.1: diphenyl phosphoryl azide; triethylamine / 1,2-dimethoxyethane / 2 h / 85 °C

With lithium hydroxide monohydrate; diphenyl phosphoryl azide; water; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane;

Reference yield:

: 1620583-23-4
ethyl 2-bromo-5-((4-chloro-2-methylphenyl)(methylsulfonyloxy)methyl)-1-isopropyl-1H-imidazole-4-carboxylate

: 1620583-22-3
8-bromo-6-(4-chloro-2-methylphenyl)-1-(5-chloro-2-methylphenyl)-7-isopropyl-6,7-dihydro-1H-purin-2(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 19 h / 4 - 20 °C

2: lithium hydroxide monohydrate; water / 1,4-dioxane / 40 h / 20 °C

3: diphenyl phosphoryl azide; triethylamine / 1,2-dimethoxyethane / 2 h / 85 °C

With lithium hydroxide monohydrate; diphenyl phosphoryl azide; water; triethylamine; In 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane;