N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

Base Information

Chemical Name:N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide
CAS No.:1404059-61-5
Molecular Formula:C₂₂H₂₃F₂N₃O₅S
Molecular Weight:479.505
Hs Code.:

Synonyms:N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

Suppliers and Price of N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

There total 6 articles about N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene 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: 70.0%

: 2905-21-7
2-fluorobenzenesulfonyl chloride

: 1404059-57-9
8-amino-3-[2-(4-fluorophenoxy)ethyl]-1,3-diazaspiro[4.5]decane-2,4-dione

: 1404059-61-5
N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1007/s00044-012-0265-x

Reference yield:

: 1404059-56-8
tert-butyl {3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}carbamate

: 1404059-61-5
N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / 1,4-dioxane / 4 h / 0 - 20 °C

2: triethylamine / dichloromethane / 16 h / 20 °C

With hydrogenchloride; triethylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1007/s00044-012-0265-x

Reference yield:

: 224309-64-2
tert-butyl N-(4-hydroxycyclohexyl)carbamate

: 1404059-61-5
N-{3-[2-(4-fluorophenoxy)ethyl]-2,4-dioxo-1,3-diazaspiro[4.5]dec-8-yl}-2-fluobenzene sulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: dimethyl sulfoxide; oxalyl dichloride / dichloromethane / 2 h / -78 °C

2: sodium cyanide / ethanol; water / 48 h / -78 - 50 °C

3: potassium carbonate / acetonitrile / 6 h / Reflux

4: hydrogenchloride / 1,4-dioxane / 4 h / 0 - 20 °C

5: triethylamine / dichloromethane / 16 h / 20 °C

With hydrogenchloride; sodium cyanide; oxalyl dichloride; potassium carbonate; dimethyl sulfoxide; triethylamine; In 1,4-dioxane; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1007/s00044-012-0265-x