5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide

Base Information

Chemical Name:5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide
CAS No.:1354786-45-0
Molecular Formula:C₂₄H₁₃ClF₄N₆O₃S₂
Molecular Weight:608.984
Hs Code.:

Synonyms:5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide

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Chemical Property of 5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide

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Technology Process of 5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide

There total 6 articles about 5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide 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: 16.0%

: 1354787-14-6
5-chloro-N-(2,4-dimethoxybenzyl)-2-fluoro-4-{2-pyridazin-4-yl-4-[2-(trifluoromethyl)-pyridine-4-yl]phenoxy}-N-1,3,4-thidiazol-2-ylbenzenesulfonamide

: 1354786-45-0
5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 20 ℃; for 5h;

Reference yield:

: 71597-85-8
(p-hydroxyphenyl)boronic acid

: 1354786-45-0
5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 18 h / 70 °C / Inert atmosphere

2: sulfuric acid; acetic acid; N-iodo-succinimide / dichloromethane / 18 h / 20 °C

3: cesium fluoride; copper(l) iodide / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / acetonitrile / 18 h / 50 °C / Inert atmosphere

4: potassium carbonate / dimethyl sulfoxide / 3 h / 20 °C

5: hydrogenchloride / 1,4-dioxane; methanol / 5 h / 20 °C

With hydrogenchloride; N-iodo-succinimide; copper(l) iodide; sulfuric acid; sodium carbonate; potassium carbonate; acetic acid; cesium fluoride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; methanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile; 1: Suzuki Coupling / 3: Stille Coupling;

Reference yield:

: 887583-90-6
4-bromo-2-(trifluoromethyl)pyridine

: 1354786-45-0
5-Chloro-2-fluoro-4-{2-(pyridazin-4-yl)-4-[2-(trifluoromethyl)pyridin-4-yl]phenoxy}-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 18 h / 70 °C / Inert atmosphere

2: sulfuric acid; acetic acid; N-iodo-succinimide / dichloromethane / 18 h / 20 °C

3: cesium fluoride; copper(l) iodide / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / acetonitrile / 18 h / 50 °C / Inert atmosphere

4: potassium carbonate / dimethyl sulfoxide / 3 h / 20 °C

5: hydrogenchloride / 1,4-dioxane; methanol / 5 h / 20 °C

With hydrogenchloride; N-iodo-succinimide; copper(l) iodide; sulfuric acid; sodium carbonate; potassium carbonate; acetic acid; cesium fluoride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; methanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile; 1: Suzuki Coupling / 3: Stille Coupling;