Benzenesulfonamide, N-[2-methoxy-6-[2-[7-methoxy-1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl] -1-[(1-methylethyl)thio]ethyl]phenyl]-4-methyl-

Base Information

Chemical Name:Benzenesulfonamide, N-[2-methoxy-6-[2-[7-methoxy-1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl] -1-[(1-methylethyl)thio]ethyl]phenyl]-4-methyl-
CAS No.:139717-78-5
Molecular Formula:C₃₅H₃₈N₂O₆S₃
Molecular Weight:678.895
Hs Code.:

Benzenesulfonamide,
N-[2-methoxy-6-[2-[7-methoxy-1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl]
-1-[(1-methylethyl)thio]ethyl]phenyl]-4-methyl-

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Chemical Property of Benzenesulfonamide, N-[2-methoxy-6-[2-[7-methoxy-1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl] -1-[(1-methylethyl)thio]ethyl]phenyl]-4-methyl-

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Technology Process of Benzenesulfonamide, N-[2-methoxy-6-[2-[7-methoxy-1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl] -1-[(1-methylethyl)thio]ethyl]phenyl]-4-methyl-

There total 4 articles about Benzenesulfonamide, N-[2-methoxy-6-[2-[7-methoxy-1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl] -1-[(1-methylethyl)thio]ethyl]phenyl]-4-methyl- 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: 18.0%

: 139717-62-7
N-tosyl-2-(2-acetoxy-1-isopropylthioethyl)-6-methoxyanilide

: 139717-63-8
N-tosyl-7-methoxyindole

: 139717-78-5
N-tosyl-3-<2-(-2-tosylamino-6-methoxyphenyl)-2-isopropylthioethyl>-7-methoxyindole

Guidance literature:: With propionic acid; for 48h; Heating;

Reference yield:

: 5862-49-7
2-(isopropylthio)ethyl acetate

: 139717-78-5
N-tosyl-3-<2-(-2-tosylamino-6-methoxyphenyl)-2-isopropylthioethyl>-7-methoxyindole

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) N-chlorosuccinimide, 2.) triethylamine / 1.) CH₂Cl₂, -30 deg C, 30 min, 2.) CH₂Cl₂, reflux, 2 h

2: 82 percent / CH₂Cl₂ / 2 h / Ambient temperature

3: 18 percent / propionic acid / 48 h / Heating

With N-chloro-succinimide; propionic acid; triethylamine; In dichloromethane;

Reference yield:

: 90-04-0
2-methoxy-phenylamine

: 139717-78-5
N-tosyl-3-<2-(-2-tosylamino-6-methoxyphenyl)-2-isopropylthioethyl>-7-methoxyindole

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) N-chlorosuccinimide, 2.) triethylamine / 1.) CH₂Cl₂, -30 deg C, 30 min, 2.) CH₂Cl₂, reflux, 2 h

2: 82 percent / CH₂Cl₂ / 2 h / Ambient temperature

3: 18 percent / propionic acid / 48 h / Heating

With N-chloro-succinimide; propionic acid; triethylamine; In dichloromethane;