3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione

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Chemical Name:3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
CAS No.:871667-65-1
Molecular Formula:C₂₅H₁₆BrClN₂O₃
Molecular Weight:507.771
Hs Code.:

Synonyms:3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione

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Chemical Property of 3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione

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Technology Process of 3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione

There total 2 articles about 3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione 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: 15.0%

: ethyl 4,5-dihydro-5-oxo-2-(p-chlorophenyl)pyrrole-3-carboxylate

: N-(p-methoxyphenyl)-p-bromobenzimidoyl chloride

: 871667-65-1
3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione

: ethyl 4-[1-p-bromophenyl-1-(p-methoxyphenylamino)methylidene]-2-chlorophenyl-4,5-dihydro-5-oxopyrrole-3-carboxylate

Guidance literature:: ethyl 4,5-dihydro-5-oxo-2-(p-chlorophenyl)pyrrole-3-carboxylate; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.5h;

N-(p-methoxyphenyl)-p-bromobenzimidoyl chloride; In tetrahydrofuran; at 20 ℃; for 48h;
DOI:10.1016/j.tet.2005.09.005

Reference yield:

: 49747-35-5
4-bromo-N-(4-methoxyphenyl)benzamide

: 871667-65-1
3-p-bromophenyl-6-p-chlorophenyl-2-p-methoxyphenyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride / 65 °C

2.1: sodium hydride / tetrahydrofuran / 0.5 h / 20 °C

2.2: 15 percent / tetrahydrofuran / 48 h / 20 °C

With thionyl chloride; sodium hydride; In tetrahydrofuran;
DOI:10.1016/j.tet.2005.09.005