5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid

Base Information

Chemical Name:5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid
CAS No.:952019-87-3
Molecular Formula:C₂₅H₂₆ClN₃O₄
Molecular Weight:467.952
Hs Code.:

Synonyms:5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid

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Chemical Property of 5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid

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Technology Process of 5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid

There total 7 articles about 5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-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: 87.0%

: 952019-86-2
5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid ethyl ester

: 952019-87-3
5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: With sodium hydroxide; In ethanol; for 18h; Heating;
DOI:10.1080/00397910701481237

Reference yield:

: 952019-77-1
2-(4-chlorophenyl)-1-(4-methoxyphenyl)-5-methyl-1H-pyrrole-3,4-dicarboxylic acid 3-tert-butyl ester 4-ethyl ester

: 952019-87-3
5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 3 h / 20 °C

2: 56 percent / Et₃N; BOP / CH₂Cl₂ / 18 h / 20 °C

3: 87 percent / aq. NaOH / ethanol / 18 h / Heating

With sodium hydroxide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; trifluoroacetic acid; In ethanol; dichloromethane;
DOI:10.1080/00397910701481237

Reference yield:

: 952019-72-6
2-acetyl-3-(4-chlorobenzoyl)succinic acid 4-tert-butyl ester 1-ethyl ester

: 952019-87-3
5-(4-chlorophenyl)-1-(4-methoxyphenyl)-2-methyl-4-(piperidin-1-ylcarbamoyl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 48 percent / AcOH / 24 h / Heating

2: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 3 h / 20 °C

3: 56 percent / Et₃N; BOP / CH₂Cl₂ / 18 h / 20 °C

4: 87 percent / aq. NaOH / ethanol / 18 h / Heating

With sodium hydroxide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; acetic acid; triethylamine; trifluoroacetic acid; In ethanol; dichloromethane; 1: Paal-Knorr cyclization;
DOI:10.1080/00397910701481237