((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

Base Information

Chemical Name:((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate
CAS No.:1563184-94-0
Molecular Formula:C₁₅H₂₃N₃O₁₀S₂
Molecular Weight:469.494
Hs Code.:

Synonyms:((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

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Chemical Property of ((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

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Technology Process of ((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

There total 5 articles about ((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate 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: 75.0%

: 1563184-93-9
((4-nitro-2-((2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)carbamoyl)phenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

: 1563184-94-0
((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

Guidance literature:: With methanol; methanesulfonyl chloride; at 20 ℃; for 0.333333h;

Reference yield:

: 7304-32-7
2-fluoro-5-nitrobenzoic acid

: 1563184-94-0
((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1.1: thionyl chloride; N,N-dimethyl-formamide / 4 h / Reflux

1.2: 0.5 h / -10 - 20 °C

2.1: triethylamine / 1,4-dioxane / 55 °C

3.1: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

4.1: methanesulfonyl chloride; methanol / 0.33 h / 20 °C

With methanol; thionyl chloride; methanesulfonyl chloride; triethylamine; N,N-dimethyl-formamide; In 1,4-dioxane; dichloromethane;

Reference yield:

: 1563184-91-7
2-fluoro-5-nitro-N-(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)benzamide

: 1563184-94-0
((2-((2-hydroxyethyl)carbamoyl)-4-nitrophenyl)azanediyl)bis(ethane-2,1-diyl)dimethanesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / 1,4-dioxane / 55 °C

2: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

3: methanesulfonyl chloride; methanol / 0.33 h / 20 °C

With methanol; methanesulfonyl chloride; triethylamine; In 1,4-dioxane; dichloromethane;