{2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

Base Information

Chemical Name:{2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester
CAS No.:148613-93-8
Molecular Formula:C₂₃H₂₅Cl₃N₂O₆S
Molecular Weight:563.886
Hs Code.:

Synonyms:{2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

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Chemical Property of {2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

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Technology Process of {2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

There total 5 articles about {2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester 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: 76.0%

: 148613-92-7
Benzyl-{2-[6,7-dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-amine

: 17341-93-4
2,2,2-Trichloroethyl chloroformate

: 148613-93-8
{2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

Guidance literature:: In acetonitrile; at 0 ℃; for 0.5h;
DOI:10.1016/S0040-4039(00)60427-6

Reference yield:

: 31165-13-6
6,7-dimethoxy-1H-indole

: 148613-93-8
{2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / diethyl ether / 1 h / 0 °C

2: 96 percent / H₂O / 3 h / 25 °C

3: 96 percent / LiAlH₄ / tetrahydrofuran; diethyl ether / 4 h / Heating

4: 90 percent / NaOH / CTAB / CH₂Cl₂ / 12 h / 25 °C

5: 76 percent / acetonitrile / 0.5 h / 0 °C

With sodium hydroxide; lithium aluminium tetrahydride; cetyltrimethylammonim bromide; In tetrahydrofuran; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4039(00)60427-6

Reference yield:

: 75909-70-5
cloruro dell'acido 6,7-dimetossindol-3-gliossilico

: 148613-93-8
{2-[6,7-Dimethoxy-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-ethyl}-methyl-carbamic acid 2,2,2-trichloro-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / H₂O / 3 h / 25 °C

2: 96 percent / LiAlH₄ / tetrahydrofuran; diethyl ether / 4 h / Heating

3: 90 percent / NaOH / CTAB / CH₂Cl₂ / 12 h / 25 °C

4: 76 percent / acetonitrile / 0.5 h / 0 °C

With sodium hydroxide; lithium aluminium tetrahydride; cetyltrimethylammonim bromide; In tetrahydrofuran; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4039(00)60427-6