1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid

Base Information

Chemical Name:1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid
CAS No.:1030617-01-6
Molecular Formula:C₁₅H₁₄N₂O₇S
Molecular Weight:366.351
Hs Code.:

Synonyms:1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid

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Chemical Property of 1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid

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Technology Process of 1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid

There total 2 articles about 1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic 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: 94.53%

: 1206465-47-5
2-[4-(3-carboxypropionylamino)benzenesulphonylamino]pentanedioic acid

: 1030617-01-6
1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid

Guidance literature:: With acetyl chloride; In benzene; at 100 ℃; for 4h;

Reference yield:

: 40686-14-4
4-(2,5-dioxopyrrolidin-1-yl)benzenesulphonyl chloride

: 1030617-01-6
1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; sodium carbonate / 2 h

2: acetyl chloride / benzene / 4 h / 100 °C

With dmap; sodium carbonate; acetyl chloride; In benzene;

Reference yield:

: 1030617-01-6
1-[4-(2,5-dioxo pyrrolidin-1-yl)benzenesulphonyl]-5-oxopyrrolidin-2-carboxylic acid

: 1370006-35-1
1-[4-(2,5-dioxopyrrolidin-1-yl)]-5-oxo-pyrrolidine-2-carboxylic acid ethyl amide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 2 h / 20 °C / Inert atmosphere

2: dmap / benzene / Inert atmosphere

With dmap; thionyl chloride; In benzene;