4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide

Base Information

• Chemical Name: 4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide
• CAS No.: 1262779-13-4
• Molecular Formula: C₁₇H₁₈N₂O₂S
• Molecular Weight: 314.408
• Mol file: 1262779-13-4.mol

Synonyms:4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide

Chemical Property of 4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide

There total 8 articles about 4-methyl-N-((1-methyl-1H-indol-2-yl)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: 87.0%

1-methyl-1H-indole-2-carboxaldehyde (27421-51-8) + toluene-4-sulfonamide (70-55-3) → 4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide (1262779-13-4)

Guidance literature:

1-methyl-1H-indole-2-carboxaldehyde; toluene-4-sulfonamide; With titanium(IV) tetraethanolate; In dichloromethane; Reflux;

With sodium tetrahydroborate; In methanol; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1002/adsc.202101126

Reference yield:

4-methyl-N-(1-methyl-1H-indol-2-ylmethylene)benzenesulfonamide (865714-25-6) → 4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide (1262779-13-4)

Guidance literature:

With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 - 20 ℃;

DOI:10.1016/j.jorganchem.2010.09.065

Reference yield:

indole (120-72-9) → 4-methyl-N-((1-methyl-1H-indol-2-yl)methyl)benzenesulfonamide (1262779-13-4)

Guidance literature:

Multi-step reaction with 4 steps

1.1: potassium hydroxide / N,N-dimethyl-formamide / 0.33 h / 0 °C

1.2: 1 h / 0 - 20 °C

2.1: n-butyllithium / diethyl ether / 3 h / 20 °C / Reflux

2.2: 3 h / Reflux

3.1: titanium(IV) tetraethanolate / toluene / 4 h / Reflux

4.1: sodium tetrahydroborate / methanol; tetrahydrofuran / 4 h / 0 - 20 °C

With titanium(IV) tetraethanolate; sodium tetrahydroborate; n-butyllithium; potassium hydroxide; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide; toluene;

DOI:10.1016/j.tet.2013.11.084

upstream raw materials:

4-methyl-N-(1-methyl-1H-indol-2-ylmethylene)benzenesulfonamide

indole

1-methylindole

ethyl N-methylindole-2-carboxylate

Downstream raw materials:

4',9-dimethyl-1',2-ditosyl-1,1',2,3,5',9-hexahydrospiro-[pyrido[3,4-b]indole-4,2'-pyrrole]

4-methyl-N-(3-(2-methyl-1-tosylaziridin-2-yl)prop-2-ynyl)-N-((1-methyl-1H-indol-2-yl)-methyl)benzenesulfonamide

N-((3-(3,3-bis(4-methoxyphenyl)-1-phenylprop-1,2-dienyl)-1-methyl-1H-indol-2-yl)methyl)-4-methylbenzenesulfonamide