4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid

Base Information

Chemical Name:4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid
CAS No.:1026398-68-4
Molecular Formula:C₁₈H₂₀N₂O₅
Molecular Weight:344.367
Hs Code.:

Synonyms:4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid

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Chemical Property of 4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid

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Technology Process of 4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid

There total 6 articles about 4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-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:

: 1-(3-Ethoxycarbonyl-propyl)-4-(4-nitro-benzoyl)-1H-pyrrole-3-carboxylic acid

: 1026398-68-4
4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 0.5h; under 1471.02 Torr;
DOI:10.1248/cpb.45.1767

Reference yield:

: 2969-81-5
Ethyl 4-bromobutyrate

: 1026398-68-4
4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaH / 1.) DMF, RT, 10 min, 2.) DMF, RT, 1.5 h

2: H₂ / 10percent Pd/C / ethanol / 0.5 h / 1471.02 Torr

With hydrogen; sodium hydride; palladium on activated charcoal; In ethanol;
DOI:10.1248/cpb.45.1767

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 1026398-68-4
4-(4-Amino-benzoyl)-1-(3-ethoxycarbonyl-propyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) AlCl₃ / 1.) CH₂Cl₂, RT, 10 min, 2.) CH₂Cl₂, RT, 2.5 h

2: 5 N aq. NaOH / dioxane / 17 h / Ambient temperature

3: 1.) NaH / 1.) DMF, RT, 10 min, 2.) DMF, RT, 1.5 h

4: H₂ / 10percent Pd/C / ethanol / 0.5 h / 1471.02 Torr

With sodium hydroxide; aluminium trichloride; hydrogen; sodium hydride; palladium on activated charcoal; In 1,4-dioxane; ethanol;
DOI:10.1248/cpb.45.1767