4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol

Base Information

Chemical Name:4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol
CAS No.:128721-44-8
Molecular Formula:C₂₄H₃₀N₂O₆S
Molecular Weight:474.578
Hs Code.:

Synonyms:4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol

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Chemical Property of 4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol

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Technology Process of 4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol

There total 7 articles about 4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol 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: 74.0%

: 67-56-1
methanol

: 128721-21-1
1-methyl-4-<2-<1-(4-methoxyphenylsulfonyl)-2-indolyl>-1,3-dithian-2-yl>-4-piperidinol

: 128721-44-8
4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol

Guidance literature:: With bis-[(trifluoroacetoxy)iodo]benzene; In water; for 0.75h; Ambient temperature;
DOI:10.3987/COM-89-5240

Reference yield:

: 120-72-9
indole

: 128721-44-8
4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 83 percent / tetrabutylammonium hydrogensulfate, 50percent aq. NaOH / benzene / 16 h / Ambient temperature

2: 1.) diisopropylamine, n-butyllithium / 1.) THF, 0 deg C, 30 min, 2.) RT, 5 h

3: 95 percent / p-toluenesulfonic acid / toluene / 15 h / Heating

4: 1.) n-butyllithium / 1.) THF, -40 deg C, 15 min, 2.) -40 deg C, 45 min

5: 74 percent / bis(trifluoroacetoxy)iodobenzene / H₂O / 0.75 h / Ambient temperature

With sodium hydroxide; n-butyllithium; tetra(n-butyl)ammonium hydrogensulfate; toluene-4-sulfonic acid; diisopropylamine; bis-[(trifluoroacetoxy)iodo]benzene; In water; toluene; benzene;
DOI:10.3987/COM-89-5240

Reference yield:

: 1445-73-4
1-Methyl-4-piperidone

: 128721-44-8
4-{Dimethoxy-[1-(4-methoxy-benzenesulfonyl)-1H-indol-2-yl]-methyl}-1-methyl-piperidin-4-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-butyllithium / 1.) THF, -40 deg C, 15 min, 2.) -40 deg C, 45 min

2: 74 percent / bis(trifluoroacetoxy)iodobenzene / H₂O / 0.75 h / Ambient temperature

With n-butyllithium; bis-[(trifluoroacetoxy)iodo]benzene; In water;
DOI:10.3987/COM-89-5240