N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide

Base Information

• Chemical Name: N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide
• CAS No.: 1579269-31-0
• Molecular Formula: C₃₂H₃₂N₂O₆S₂
• Molecular Weight: 604.748

Synonyms:N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide

Chemical Property of N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide

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Technology Process of N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide

There total 1 articles about N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide 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: 85.0%

2-iodo-N-Ts-indole (1257657-62-7) + N-(4-Methoxy-benzyl)-4-methyl-N-(2-oxo-ethyl)-benzenesulfonamide (54879-58-2) → N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide (1579269-31-0)

Guidance literature:

2-iodo-N-Ts-indole; With isopropylmagnesium chloride; In tetrahydrofuran; at 0 ℃; for 0.25h;

N-(4-Methoxy-benzyl)-4-methyl-N-(2-oxo-ethyl)-benzenesulfonamide; In tetrahydrofuran; at 0 ℃; for 1.5h;

DOI:10.1016/j.tet.2014.01.074

Reference yield: 47.0%

N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide (1579269-31-0) → 4-(4-methoxyphenyl)-2,5-ditosyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (1579269-36-5) + N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-4-methylbenzenesulfonamide (1579269-40-1)

Guidance literature:

With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1.5h;

DOI:10.1016/j.tet.2014.01.074

upstream raw materials:

2-iodo-N-Ts-indole

N-(4-Methoxy-benzyl)-4-methyl-N-(2-oxo-ethyl)-benzenesulfonamide

Downstream raw materials:

4-(4-methoxyphenyl)-2,5-ditosyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

N-(2-hydroxy-2-(1-tosyl-1H-indol-2-yl)ethyl)-4-methylbenzenesulfonamide

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