(R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

Base Information

Chemical Name:(R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline
CAS No.:1383456-24-3
Molecular Formula:C₃₁H₂₆N₂O₂S
Molecular Weight:490.626
Hs Code.:

Synonyms:(R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

Suppliers and Price of (R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

There total 4 articles about (R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline 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:

: 120-72-9
indole

: 1383456-17-4
4-methyl-N-(4-methyl-2-(phenylethynyl)benzylidene)benzenesulfonamide

: (S)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

: 1383456-24-3
(R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

Guidance literature:: With Ag⁽¹⁺⁾*C₅₂H₆₀O₄P^(1-); In toluene; at 40 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere; Darkness;
DOI:10.1016/j.tet.2012.02.058

Reference yield:

: 824-54-4
2-bromo-4-methylbenzaldehyde

: (S)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

: 1383456-24-3
(R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 4 h / 50 °C / Inert atmosphere

2: titanium(IV) tetraethanolate / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

3: Ag⁽¹⁺⁾*C₅₂H₆₀O₄P^(1-) / toluene / 40 °C / Inert atmosphere; Darkness

With bis-triphenylphosphine-palladium(II) chloride; titanium(IV) tetraethanolate; copper(l) iodide; Ag⁽¹⁺⁾*C₅₂H₆₀O₄P^(1-); triethylamine; In tetrahydrofuran; toluene; 3: Friedel Crafts alkylation;
DOI:10.1016/j.tet.2012.02.058

Reference yield:

: 536-74-3
phenylacetylene

: (S)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

: 1383456-24-3
(R)-1-(1H-indol-3-yl)-6-methyl-3-phenyl-2-tosyl-1,2-dihydroisoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 4 h / 50 °C / Inert atmosphere

2: titanium(IV) tetraethanolate / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere

3: Ag⁽¹⁺⁾*C₅₂H₆₀O₄P^(1-) / toluene / 40 °C / Inert atmosphere; Darkness

With bis-triphenylphosphine-palladium(II) chloride; titanium(IV) tetraethanolate; copper(l) iodide; Ag⁽¹⁺⁾*C₅₂H₆₀O₄P^(1-); triethylamine; In tetrahydrofuran; toluene; 3: Friedel Crafts alkylation;
DOI:10.1016/j.tet.2012.02.058