4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid

Base Information

Chemical Name:4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid
CAS No.:128477-47-4
Molecular Formula:C₁₈H₁₈N₄O₈S
Molecular Weight:450.429
Hs Code.:

Synonyms:4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid

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Chemical Property of 4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid

Chemical Property:

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Technology Process of 4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid

There total 3 articles about 4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric 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: 84.7%

: 127605-21-4
1-<4'-(4''-nitrobenzoyl)aminobenzenesulphonyl>-5-oxo-pyrrolidine-2-carboxylic acid

: 128477-47-4
4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid

Guidance literature:: With ammonia; In water;

Reference yield:

: 62595-79-3,64598-89-6
4-acetamido benzenesulphonyl-(L)-(+)-glutamic acid

: 128477-47-4
4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid

Guidance literature:: Multi-step reaction with 4 steps

1: 1. 2 N HCl 2. NH₃

2: 77 percent / benzene; diethyl ether / 2.5 h / Heating

3: 79 percent / acetyl chloride / 2 h / Heating

4: 84.7 percent / NH₃ / H₂O

With hydrogenchloride; ammonia; acetyl chloride; In diethyl ether; water; benzene;

Reference yield:

: 127605-17-8
4-(4'-nitrobenzoyl)aminobenzenesulphonyl-L-(+)-glutamic acid

: 128477-47-4
4-Carbamoyl-2-[4-(4-nitro-benzoylamino)-benzenesulfonylamino]-butyric acid

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / acetyl chloride / 2 h / Heating

2: 84.7 percent / NH₃ / H₂O

With ammonia; acetyl chloride; In water;