4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide

Base Information

Chemical Name:4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide
CAS No.:1446444-65-0
Molecular Formula:C₂₄H₂₄ClF₂N₃O₆S
Molecular Weight:555.987
Hs Code.:

Synonyms:4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide

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Chemical Property of 4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide

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Technology Process of 4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide

There total 6 articles about 4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide 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: 11.0%

: 1446444-66-1
4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluorobenzoic acid

: 15211-35-5
N-(4-methoxybenzyl)-N-methylsulfamide

: 1446444-65-0
4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 96h; Inert atmosphere;

Reference yield:

: 1355066-41-9
5-chloro-6-(1-propan-2-yloxy)-3-pyridinol

: 1446444-65-0
4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dimethyl sulfoxide / 18 h / 170 °C / Inert atmosphere

2: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 96 h / 20 °C / Inert atmosphere

With dmap; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; dimethyl sulfoxide;

Reference yield:

: 1344997-94-9
3-chloro-2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

: 1446444-65-0
4-((5-chloro-6-isopropoxypyridin-3-yl)oxy)-2,5-difluoro-N-(N-(4-methoxybenzyl)-N-methylsulfamoyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: peracetic acid; acetic acid / water / 4 h / 5 - 20 °C

2: potassium carbonate / dimethyl sulfoxide / 18 h / 170 °C / Inert atmosphere

3: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 96 h / 20 °C / Inert atmosphere

With peracetic acid; dmap; potassium carbonate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; water; dimethyl sulfoxide;