2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde

Base Information

Chemical Name:2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde
CAS No.:1442652-32-5
Molecular Formula:C₁₉H₁₆FNO₃S
Molecular Weight:357.405
Hs Code.:

Synonyms:2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde

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Chemical Property of 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde

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Technology Process of 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde

There total 4 articles about 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde 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: 95.0%

: 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-(fluoro)phenyl]-1H-pyrrole

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 1442652-32-5
2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde

Guidance literature:: With trichlorophosphate; In dichloromethane; at 0 ℃; for 1.05h; regioselective reaction; Reflux;
DOI:10.1016/j.bmc.2013.04.031

Reference yield:

: 3446-89-7
4-(Methylthio)benzaldehyde

: 1442652-32-5
2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide / 0.25 h / 70 °C / 7757.43 Torr / Microwave irradiation

2: oxone / methanol; water / 2.08 h / 25 °C

3: toluene-4-sulfonic acid / ethanol / 0.75 h / 160 °C / 7757.43 Torr / Microwave irradiation

4: trichlorophosphate / dichloromethane / 1.05 h / 0 °C / Reflux

With oxone; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; toluene-4-sulfonic acid; triethylamine; trichlorophosphate; In methanol; ethanol; dichloromethane; water; 1: |Stetter 1,4-Dicarbonyl Synthesis / 3: |Paal-Knorr Pyrrole Synthesis;
DOI:10.1016/j.bmc.2013.04.031

Reference yield:

: 189501-34-6
1-[4-(methylsulfonyl)phenyl]pentane-1,4-dione

: 1442652-32-5
2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3-fluorophenyl]-1H-pyrrole-3-carboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / ethanol / 0.75 h / 160 °C / 7757.43 Torr / Microwave irradiation

2: trichlorophosphate / dichloromethane / 1.05 h / 0 °C / Reflux

With toluene-4-sulfonic acid; trichlorophosphate; In ethanol; dichloromethane; 1: |Paal-Knorr Pyrrole Synthesis;
DOI:10.1016/j.bmc.2013.04.031