2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid

Base Information

Chemical Name:2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid
CAS No.:214843-55-7
Molecular Formula:C₁₉H₂₀N₄O₅S₃
Molecular Weight:480.59
Hs Code.:

Synonyms:2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid

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Chemical Property of 2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid

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Technology Process of 2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid

There total 4 articles about 2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid 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: 98.0%

: 214843-36-4
2-[2-(4-Cyano-benzenesulfonylamino)-acetylamino]-3-(4-cyano-phenyl)-propionic acid

: 214843-55-7
2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid

Guidance literature:: With pyridine; hydrogen sulfide; triethylamine; for 120h;
DOI:10.1021/jm980227t

Reference yield:

: 49584-26-1
p-cyanobenzenesulfonyl chloride

: 214843-55-7
2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / 1 M NaOH / diethyl ether / 20 h / Ambient temperature

2: 91 percent / DCCl / dioxane / 4 °C

3: 75 percent / Et₃N / dimethylformamide / 96 h

4: 98 percent / H₂S, Et₃N, pyridine / 120 h

With pyridine; sodium hydroxide; hydrogen sulfide; triethylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/jm980227t

Reference yield:

: 214841-99-3
((4-cyanophenyl)sulfonyl)glycine

: 214843-55-7
2-[2-(4-Thiocarbamoyl-benzenesulfonylamino)-acetylamino]-3-(4-thiocarbamoyl-phenyl)-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / DCCl / dioxane / 4 °C

2: 75 percent / Et₃N / dimethylformamide / 96 h

3: 98 percent / H₂S, Et₃N, pyridine / 120 h

With pyridine; hydrogen sulfide; triethylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/jm980227t