N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide

Base Information

• Chemical Name: N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide
• CAS No.: 136138-34-6
• Molecular Formula: C₂₁H₁₇FINO₄S
• Molecular Weight: 525.339
• Mol file: 136138-34-6.mol

Synonyms:N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide

Chemical Property of N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide

There total 1 articles about N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide 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:

2-Fluoro-N-(2-iodo-phenyl)-6-methoxy-benzamide (136138-49-3) + p-toluenesulfonyl chloride (98-59-9) → N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide (136138-34-6)

Guidance literature:

With sodium hydride; at -78 - 25 ℃;

DOI:10.1039/c39910001046

Reference yield: 83.0%

N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide (136138-34-6) → N-[2-(2-Fluoro-6-methoxy-benzoyl)-phenyl]-4-methyl-benzenesulfonamide (136138-38-0)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; diethyl ether; hexane; at -100 - -70 ℃; for 0.25h;

DOI:10.1039/c39910001046

Reference yield:

N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide (136138-34-6) → 1-methoxy-9-oxo-9,10-dihydroacridine (6950-01-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 83 percent / n-BuLi / tetrahydrofuran; diethyl ether; hexane / 0.25 h / -100 - -70 °C

2: Et₄NOH / tetrahydrofuran; methanol / Heating

With n-butyllithium; tetraethylammonium hydroxide; In tetrahydrofuran; methanol; diethyl ether; hexane;

DOI:10.1039/c39910001046

upstream raw materials:

2-Fluoro-N-(2-iodo-phenyl)-6-methoxy-benzamide

p-toluenesulfonyl chloride

Downstream raw materials:

N-[2-(2-Fluoro-6-methoxy-benzoyl)-phenyl]-4-methyl-benzenesulfonamide

1-methoxy-9-oxo-9,10-dihydroacridine