3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

Base Information

Chemical Name:3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide
CAS No.:318466-90-9
Molecular Formula:C₃₃H₄₃N₇O₁₄S₃
Molecular Weight:857.941
Hs Code.:

3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

Synonyms:3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

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Chemical Property of 3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

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Technology Process of 3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

There total 9 articles about 3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide 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: 99.0%

: 318466-89-6
3-[{3-[[5-(tert-butyldimethylsilanyloxy)pentyl](2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

: 318466-90-9
3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

Guidance literature:: With hydrogen fluoride; In acetonitrile; at 20 ℃; for 0.0333333h;

Reference yield:

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 318466-90-9
3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

Guidance literature:: Multi-step reaction with 5 steps

1: 87 percent / triethylamine / CH₂Cl₂ / 0.5 h / 20 °C

2: 49 percent / Ph₃P; DEAD / toluene / 0.17 h / 20 °C

3: 86 percent / pyrrolidine / Pd(PPh₃)4 / CH₂Cl₂ / 0.5 h / 20 °C

4: 74 percent / DCC / acetonitrile / 0.33 h / 20 °C

5: 50 mg / aqueous hydrofluoric acid / acetonitrile / 0.03 h / 0 °C

With pyrrolidine; hydrogen fluoride; triethylamine; dicyclohexyl-carbodiimide; triphenylphosphine; diethylazodicarboxylate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In dichloromethane; toluene; acetonitrile; 2: Mitsunobu reaction;
DOI:10.1016/S0040-4020(02)00626-9

Reference yield:

: 196214-23-0
N-(3-hydroxypropyl)-2-nitrobenzenesulfonamide

: 318466-90-9
3-[{3-[(5-hydroxypentyl)(2-nitrobenzenesulfonyl)amino]propyl}(2-nitrobenzenesulfonyl)amino]-N-[3-(2-nitrobenzenesulfonylamino)propyl]butyramide

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / cesium carbonate / acetonitrile / 15 h / 60 °C

2: 49 percent / Ph₃P; DEAD / toluene / 0.17 h / 20 °C

3: 86 percent / pyrrolidine / Pd(PPh₃)4 / CH₂Cl₂ / 0.5 h / 20 °C

4: 74 percent / DCC / acetonitrile / 0.33 h / 20 °C

5: 50 mg / aqueous hydrofluoric acid / acetonitrile / 0.03 h / 0 °C

With pyrrolidine; hydrogen fluoride; caesium carbonate; dicyclohexyl-carbodiimide; triphenylphosphine; diethylazodicarboxylate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In dichloromethane; toluene; acetonitrile; 2: Mitsunobu reaction;
DOI:10.1016/S0040-4020(02)00626-9