3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine

Base Information

Chemical Name:3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine
CAS No.:83055-24-7
Molecular Formula:C₆H₁₃N*C₃₂H₃₂ClNO₆
Molecular Weight:661.238
Hs Code.:

3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine

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Chemical Property of 3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine

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Technology Process of 3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine

There total 6 articles about 3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine 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:

: 15649-02-2
ethyl p-isobutylphenyl acetate

: 83055-24-7
3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine

Guidance literature:: Multi-step reaction with 4 steps

1: sodium ethylate / ethanol; dimethylsulfoxide / 0.5 h / Ambient temperature

2: 38 percent / aq. NaOH / ethanol / 1) reflux, 5 min, 2) R_.T_., 3 h

3: 57 percent

With sodium hydroxide; sodium ethanolate; In ethanol; dimethyl sulfoxide;

Reference yield:

: 109134-99-8
ethyl ester of p-isobutyl-2-phenyl-3-hydroxypropane acid

: 83055-24-7
3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-isobutyl-phenyl)-propionic acid; compound with cyclohexylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / aq. NaOH / ethanol / 1) reflux, 5 min, 2) R_.T_., 3 h

2: 57 percent

With sodium hydroxide; In ethanol;