N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide

Base Information

• Chemical Name: N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide
• CAS No.: 1447159-66-1
• Molecular Formula: C₂₂H₁₈IN₃O₄S₂
• Molecular Weight: 579.439
• Mol file: 1447159-66-1.mol

Synonyms:N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide

Chemical Property of N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide

There total 1 articles about N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide 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: 43.0%

N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide (1404202-56-7) + 5-nitro-1-(prop-1-en-1-yl)-1H-indole (146852-16-6) → N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide (1447159-66-1)

Guidance literature:

With iodine; caesium carbonate; In acetonitrile; at 20 ℃; for 4h; Inert atmosphere;

DOI:10.1039/c3cc42309c

Reference yield: 73.0%

N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide (1447159-66-1) → N-(4-methyl-2-(7-nitro-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)phenyl)thiophene-2-sulfonamide (1447159-88-7)

Guidance literature:

N-(1-allyl-5-nitro-1H-indol-2-yl)-N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide; With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; triethylamine; In N,N-dimethyl-formamide; at 130 ℃; for 7h; Inert atmosphere;

DOI:10.1039/c3cc42309c

upstream raw materials:

N-(2-iodo-4-methylphenyl)thiophene-2-sulfonamide

5-nitro-1-(prop-1-en-1-yl)-1H-indole

Downstream raw materials:

N-(4-methyl-2-(7-nitro-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)phenyl)thiophene-2-sulfonamide