3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid

Base Information

• Chemical Name: 3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid
• CAS No.: 910239-65-5
• Molecular Formula: C₃₀H₂₈N₂O₈
• Molecular Weight: 544.561

Synonyms:3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid

Chemical Property of 3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid

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Technology Process of 3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid

There total 3 articles about 3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid 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: 89.0%

3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid ethyl ester → 3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid (910239-65-5)

Guidance literature:

With potassium hydroxide; In ethanol; water; for 24h; Heating;

DOI:10.1016/j.tet.2006.06.047

Reference yield:

3-iodo-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid ethyl ester (848757-53-9) → 3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid (910239-65-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / 1,8-diazabicyclo[5.4.0]undec-7-ene; Pd(OAc)2 / tetrahydrofuran / 0.67 h / 10 °C / microwave irradiation

2: 89 percent / KOH / ethanol; H₂O / 24 h / Heating

With palladium diacetate; potassium hydroxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; ethanol; water;

DOI:10.1016/j.tet.2006.06.047

Reference yield:

2,4-Dimethoxybenzylamine (20781-20-8) → 3-((2,4-dimethoxybenzyl)carbamoyl)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid (910239-65-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / 1,8-diazabicyclo[5.4.0]undec-7-ene; Pd(OAc)2 / tetrahydrofuran / 0.67 h / 10 °C / microwave irradiation

2: 89 percent / KOH / ethanol; H₂O / 24 h / Heating

With palladium diacetate; potassium hydroxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; ethanol; water;

DOI:10.1016/j.tet.2006.06.047

upstream raw materials:

3-iodo-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid ethyl ester

2,4-Dimethoxybenzylamine

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