N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide

Base Information

Chemical Name:N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide
CAS No.:1295567-55-3
Molecular Formula:C₂₀H₁₉F₂IN₄O₅S₂
Molecular Weight:624.428
Hs Code.:

Synonyms:N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide

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Chemical Property of N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide

Chemical Property:

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Technology Process of N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide

There total 7 articles about N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide 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:

: 1295567-67-7
N-(3-{2-amino-5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]phenoxy}phenyl)ethanesulfonamide

: 1295567-55-3
N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide

Guidance literature:: With sulphamoyl chloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 96h;

Reference yield:

: 29632-74-4
2-fluro-4-iodoaniline

: 1295567-55-3
N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 121 h / -10 - 0 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 72 h / 20 °C

2.2: 20 h / 20 °C / Inert atmosphere

2.3: 3 h / 50 °C

3.1: N-ethyl-N,N-diisopropylamine; sulphamoyl chloride / dichloromethane / 96 h / 20 °C

With sulphamoyl chloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 315-14-0
1,3,5-trifluoro-2-nitrobenzene

: 1295567-55-3
N-(3-{5-fluoro-3-[(2-fluoro-4-iodophenyl)amino]-2-(sulfamoylamino)phenoxy}phenyl)ethanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 121 h / -10 - 0 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 72 h / 20 °C

2.2: 20 h / 20 °C / Inert atmosphere

2.3: 3 h / 50 °C

3.1: N-ethyl-N,N-diisopropylamine; sulphamoyl chloride / dichloromethane / 96 h / 20 °C

With sulphamoyl chloride; potassium carbonate; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;