5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide

Base Information

Chemical Name:5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide
CAS No.:1354787-43-1
Molecular Formula:C₁₉H₁₆ClF₂N₃O₄S
Molecular Weight:455.87
Hs Code.:

Synonyms:5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide

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Chemical Property of 5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide

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Technology Process of 5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide

There total 5 articles about 5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-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: 89.7%

: 1354787-44-2
N-[(2,4-dimethoxyphenyl)methyl]pyrimidin-4-amine

: 13656-57-0
5-chloro-2,4-difluorobenzene-1-sulfonyl chloride

: 1354787-43-1
5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; In ethyl acetate; at 20 - 30 ℃; for 1.5h;

Reference yield: 26.0%

: 1354787-43-1
5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; In acetonitrile; at 20 ℃; for 1h; Cooling with ice;

Reference yield:

: 20781-20-8
2,4-Dimethoxybenzylamine

: 1354787-43-1
5-chloro-N-[(2,4-dimethoxyphenyl)methyl]-2,4-difluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / butan-1-ol / 2 h / 100 °C

2: ammonium formate / palladium 10% on activated carbon / ethanol / 2 h / 80 °C

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 18 h / 20 °C

With ammonium formate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In ethanol; acetonitrile; butan-1-ol;