6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester

Base Information

Chemical Name:6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester
CAS No.:157977-16-7
Molecular Formula:C₃₀H₃₀ClNO₇S
Molecular Weight:584.09
Hs Code.:

Synonyms:6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester

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Chemical Property of 6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester

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Technology Process of 6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester

There total 3 articles about 6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester 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:

: 62655-56-5
2-(4'-methoxy-phenyl)-6-methoxy-indole

: 157977-16-7
6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 1.6M n-BuLi / 1.) THF, C₆H₁₄, -78 deg C, 3 h, 2.) THF, C₆H₁₄, -78 deg C to r.t., overnight

2: 55 percent / AlCl₃ / CH₂Cl₂ / 1 h

With n-butyllithium; aluminium trichloride; In dichloromethane;
DOI:10.1002/ardp.19943270602

Reference yield:

: 626-86-8
adipinic acid monoethyl ester

: 157977-16-7
6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 0.5 h / 100 °C

2: 55 percent / AlCl₃ / CH₂Cl₂ / 1 h

With aluminium trichloride; thionyl chloride; In dichloromethane;
DOI:10.1002/ardp.19943270602

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 157977-16-7
6-<3-Chlor-6-methoxy-2-(4-methoxyphenyl)-1-phenylsulfonyl-indol-5-yl>-6-oxohexansaeure-Ethylester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 1.6M n-BuLi / 1.) THF, C₆H₁₄, -78 deg C, 3 h, 2.) THF, C₆H₁₄, -78 deg C to r.t., overnight

2: 55 percent / AlCl₃ / CH₂Cl₂ / 1 h

With n-butyllithium; aluminium trichloride; In dichloromethane;
DOI:10.1002/ardp.19943270602