1-(4-Methoxybenzene-1-sulfonyl)-2-methyl-1H-indole-3-carbaldehyde

Base Information

• Chemical Name: 1-(4-Methoxybenzene-1-sulfonyl)-2-methyl-1H-indole-3-carbaldehyde
• CAS No.: 80664-26-2
• Molecular Formula: C17H15NO4S
• Molecular Weight: 329.376
• DSSTox Substance ID: DTXSID20539569
• Wikidata: Q82415347

Synonyms:80664-26-2;1-((4-Methoxyphenyl)sulfonyl)-2-methyl-1H-indole-3-carbaldehyde;DTXSID20539569;1-(4-Methoxybenzene-1-sulfonyl)-2-methyl-1H-indole-3-carbaldehyde

Chemical Property of 1-(4-Methoxybenzene-1-sulfonyl)-2-methyl-1H-indole-3-carbaldehyde

Chemical Property:

• XLogP3: 3.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 329.07217913
• Heavy Atom Count: 23
• Complexity: 521

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C2=CC=CC=C2N1S(=O)(=O)C3=CC=C(C=C3)OC)C=O

Technology Process of 1-(4-Methoxybenzene-1-sulfonyl)-2-methyl-1H-indole-3-carbaldehyde

There total 9 articles about 1-(4-Methoxybenzene-1-sulfonyl)-2-methyl-1H-indole-3-carbaldehyde 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: 53.0%

N-<<(4-methoxybenzenesulfonyl)-1H-indol-3-yl>methylene>-2-methyl-2-propanamine (81816-16-2) + trimethylsilylmethoxytris(dimethylamino) phosphonium trifluoromethanesulfonate → N-<<(4-methoxybenzenesulfonyl)-2-methyl-1H-indol-3-yl>methylene>-2-methyl-2-propanamine (81816-17-3) + tert-Butyl-[1-[1-(4-methoxy-benzenesulfonyl)-2-trimethylsilanylmethyl-1H-indol-3-yl]-meth-(E)-ylidene]-amine + N-<(4-methoxyphenyl)sulfonyl>-2-methylindole-3-carboxaldehyde (80664-26-2)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; hexane; -78 deg C, 4 h. then room temp.;

DOI:10.1016/S0040-4020(01)93262-4

Reference yield: 51.0%

chloro-trimethyl-silane (75-77-4) + N-<<(4-methoxybenzenesulfonyl)-2-methyl-1H-indol-3-yl>methylene>-2-methyl-2-propanamine (81816-17-3) → tert-Butyl-[1-[1-(4-methoxy-2-trimethylsilanyl-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-meth-(E)-ylidene]-amine + N-<(4-methoxyphenyl)sulfonyl>-2-methylindole-3-carboxaldehyde (80664-26-2)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; hexane; -78 deg C then room temp.;

DOI:10.1016/S0040-4020(01)93262-4

Reference yield: 45.0%

2-methyl-1H-indole-3-carbaldehyde (5416-80-8) + 4-methoxy-phenyl-sulphonyl chloride (98-68-0) → N-<(4-methoxyphenyl)sulfonyl>-2-methylindole-3-carboxaldehyde (80664-26-2)

Guidance literature:

With 1H-imidazole; sodium hydride;

DOI:10.1016/S0040-4020(01)93262-4

upstream raw materials:

chloro-trimethyl-silane

N-<<(4-methoxybenzenesulfonyl)-2-methyl-1H-indol-3-yl>methylene>-2-methyl-2-propanamine

2-methyl-1H-indole-3-carbaldehyde

4-methoxy-phenyl-sulphonyl chloride

Downstream raw materials:

But-3-enyl-[1-[1-(4-methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-meth-(E)-ylidene]-amine

N-<<(4-methoxybenzenesulfonyl)-2-methyl-1H-indol-3-yl>methylene>-4-pentenylamine

[1-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-meth-(E)-ylidene]-(2-phenylsulfanyl-ethyl)-amine

(E)-1-<(p-methoxyphenyl)sulfonyl>-2-methyl-3-indole

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