[1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester

Base Information

• Chemical Name: [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester
• CAS No.: 926291-40-9
• Molecular Formula: C₂₂H₁₉BrN₂O₄
• Molecular Weight: 455.308

Synonyms:[1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester

Chemical Property of [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester

Chemical Property:

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Technology Process of [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester

There total 2 articles about [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester 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: 72.0%

(2,3-dihydroindol-3-yl)acetic acid methyl ester (85676-99-9) + N-benzyl-2,3-dibromo-maleimide (91026-00-5) → [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester (926291-40-9)

Guidance literature:

With triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

DOI:10.1007/s11094-006-0147-y

Reference yield:

Indole-3-acetic acid methyl ester (1912-33-0) → [1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester (926291-40-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 70 percent / NaBH₃CN / acetic acid

2: 72 percent / Et₃N / dimethylformamide / 12 h / 20 °C

With sodium cyanoborohydride; triethylamine; In acetic acid; N,N-dimethyl-formamide;

DOI:10.1007/s11094-006-0147-y

Reference yield:

[1-(1-benzyl-4-bromo-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-2,3-dihydro-1H-indol-3-yl]acetic acid methyl ester (926291-40-9) → {1-[1-benzyl-4-(2,3-dihydro-1H-indol-1-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl]-1H-indol-3-yl}acetic acid methyl ester (926291-42-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 72 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / toluene / 1 h / Heating

2: 70 percent / Et₃N / dimethylformamide / 24 h / 20 °C

With triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In N,N-dimethyl-formamide; toluene;

DOI:10.1007/s11094-006-0147-y

upstream raw materials:

(2,3-dihydroindol-3-yl)acetic acid methyl ester

N-benzyl-2,3-dibromo-maleimide

Indole-3-acetic acid methyl ester

Downstream raw materials:

{1-[1-benzyl-4-(2,3-dihydro-1H-indol-1-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl]-1H-indol-3-yl}acetic acid methyl ester

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