4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide

Base Information

Chemical Name:4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide
CAS No.:855249-00-2
Molecular Formula:C₂₉H₂₇FN₂O₃
Molecular Weight:470.543
Hs Code.:

Synonyms:4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide

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Chemical Property of 4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide

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Technology Process of 4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide

There total 10 articles about 4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide 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:

: 1027039-32-2
C₂₁H₁₇ClFNO₂

: 2393-23-9
4-methoxy-benzylamine

: 855249-00-2
4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1016/j.tet.2007.06.005

Reference yield:

: 855231-02-6
4-(4-fluoro-phenyl)-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid ethyl ester

: 855249-00-2
4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide

Guidance literature:: Multi-step reaction with 4 steps

1: POCl₃ / 1,2-dichloro-ethane / 3 h / 80 °C

2: 100 percent / NaOH / methanol / 2 h / 60 °C

3: SOCl₂ / 80 °C

4: Et₃N / tetrahydrofuran / 12 h / 25 °C

With sodium hydroxide; thionyl chloride; triethylamine; trichlorophosphate; In tetrahydrofuran; methanol; 1,2-dichloro-ethane; 1: Vilsmeir-Haack reaction;
DOI:10.1016/j.bmcl.2007.05.096

Reference yield:

: 855231-04-8
4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid ethyl ester

: 855249-00-2
4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid 4-methoxybenzylamide

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / NaOH / methanol / 2 h / 60 °C

2: SOCl₂ / 80 °C

3: Et₃N / tetrahydrofuran / 12 h / 25 °C

With sodium hydroxide; thionyl chloride; triethylamine; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2007.05.096