N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide

Base Information

Chemical Name:N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide
CAS No.:1425486-29-8
Molecular Formula:C₂₁H₂₀F₃N₃O₅S₂
Molecular Weight:515.534
Hs Code.:

Synonyms:N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide

Chemical Property:

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Technology Process of N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide

There total 6 articles about N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide 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: 33.0%

: 10147-36-1
n-propanesulfonyl chloride

: 1425487-57-5
(3-amino-2,5,6-trifluorophenyl)(quinoxalin-6-yl)methanone

: 1425486-29-8
N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide

Guidance literature:: With triethylamine; In 1,4-dioxane; dichloromethane; at 20 ℃; for 1h;

Reference yield:

: 367-34-0
2,4,5-trifluoroaniline

: 1425486-29-8
N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydrogencarbonate / 1,4-dioxane; water / 20 °C

2.1: n-butyllithium / tetrahydrofuran / 0.5 h / -78 °C

2.2: 1 h / -78 °C

3.1: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C

4.1: triethylamine / 1,4-dioxane; dichloromethane / 1 h / 20 °C

With hydrogenchloride; n-butyllithium; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

Reference yield:

: 875558-38-6
N-methoxy-N-methylquinoxaline-6-carboxamide

: 1425486-29-8
N-(propylsulfonyl)-N-(2,4,5-trifluoro-3-(quinoxaline-6-carbonyl)phenyl)propane-1-sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran / 0.5 h / -78 °C

1.2: 1 h / -78 °C

2.1: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C

3.1: triethylamine / 1,4-dioxane; dichloromethane / 1 h / 20 °C

With hydrogenchloride; n-butyllithium; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;