{2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester

Base Information

Chemical Name:{2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester
CAS No.:1571842-04-0
Molecular Formula:C₂₀H₁₈N₂O₆S
Molecular Weight:414.439
Hs Code.:

Synonyms:{2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester

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Chemical Property of {2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester

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Technology Process of {2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester

There total 3 articles about {2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl 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: 68.0%

: 1571841-86-5
[2-(1H-indol-3-yl)-2-oxo-acetylamino]acetic acid methyl ester

: 98-59-9
p-toluenesulfonyl chloride

: 1571842-04-0
{2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester

Guidance literature:: With sodium hydride; In acetonitrile; at 0 - 5 ℃; for 0.5h;
DOI:10.1016/j.bmc.2014.01.027

Reference yield:

: 120-72-9
indole

: 1571842-04-0
{2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: diethyl ether / 0 °C

2: potassium carbonate / acetonitrile / 0 - 5 °C

3: sodium hydride / acetonitrile / 0.5 h / 0 - 5 °C

With sodium hydride; potassium carbonate; In diethyl ether; acetonitrile;
DOI:10.1016/j.bmc.2014.01.027

Reference yield:

: 22980-09-2
indolyl-3-glyoxylyl chloride

: 1571842-04-0
{2-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]acetylamino}acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 0 - 5 °C

2: sodium hydride / acetonitrile / 0.5 h / 0 - 5 °C

With sodium hydride; potassium carbonate; In acetonitrile;
DOI:10.1016/j.bmc.2014.01.027