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

Base Information

• Chemical Name: 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-difluorophenyl]-1H-pyrrole-3-carboxaldehyde
• CAS No.: 1442652-33-6
• Molecular Formula: C₁₉H₁₅F₂NO₃S
• Molecular Weight: 375.396
• Mol file: 1442652-33-6.mol

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

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

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

There total 4 articles about 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-difluorophenyl]-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%

N,N-dimethyl-formamide (68-12-2,33513-42-7) + 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-(difluoro)phenyl]-1H-pyrrole (189500-98-9) → 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-difluorophenyl]-1H-pyrrole-3-carboxaldehyde (1442652-33-6)

Guidance literature:

With trichlorophosphate; In dichloromethane; at 0 ℃; for 1.05h; regioselective reaction; Reflux;

DOI:10.1016/j.bmc.2013.04.031

Reference yield:

4-(Methylthio)benzaldehyde (3446-89-7) → 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-difluorophenyl]-1H-pyrrole-3-carboxaldehyde (1442652-33-6)

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:

1-[4-(methylsulfonyl)phenyl]pentane-1,4-dione (189501-34-6) → 2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-difluorophenyl]-1H-pyrrole-3-carboxaldehyde (1442652-33-6)

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

upstream raw materials:

4-(Methylthio)benzaldehyde

N,N-dimethyl-formamide

2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-(difluoro)phenyl]-1H-pyrrole

1-[4-(methylthio)phenyl]pentane-1,4-dione

Downstream raw materials:

2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-difluorophenyl]-1H-pyrrole-3-carboxime

2-methyl-5-[4-(methylsulfonyl)phenyl]-1-[3,4-difluorophenyl]-1H-pyrrole-3-carbonitrile