N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide

Base Information

Chemical Name:N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide
CAS No.:1616380-37-0
Molecular Formula:C₂₂H₂₂FN₅O₄
Molecular Weight:439.446
Hs Code.:

Synonyms:N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide

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Chemical Property of N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide

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Technology Process of N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide

There total 13 articles about N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide 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:

: 1616380-71-2
5-((4-((3-aminophenyl)amino)-5-fluoropyrimidin-2-yl)amino)-2-(2-methoxyethoxyl)phenol

: 814-68-6,25189-84-8
acryloyl chloride

: 1616380-37-0
N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide

Guidance literature:: In dichloromethane; at -30 ℃;

Reference yield:

: 1616380-60-9
2-(benzyloxy)-1-(2-methoxyethoxy)-4-nitrobenzene

: 1616380-37-0
N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 5 steps

1: ethanol; tin(ll) chloride / 3 h / 80 °C

2: acetic acid / ethanol / 24 h / Reflux

3: palladium on activated charcoal; hydrogen / ethanol / 50 h / 20 °C / 7240.26 Torr / Autoclave; Inert atmosphere

4: trifluoroacetic acid / dichloromethane / 0.75 h / 0 - 20 °C

5: dichloromethane / -30 °C

With ethanol; palladium on activated charcoal; hydrogen; acetic acid; trifluoroacetic acid; tin(ll) chloride; In ethanol; dichloromethane;

Reference yield:

: 1202759-89-4
tert-butyl (3-((2-chloro-5-fluoropyrimidin-4-yl)amino)phenyl)carbamate

: 1616380-37-0
N-(3-((5-fluoro-2-((3-hydroxy-4-(2-methoxyethoxyl)phenyl)amino)pyrimidin-4-yl)amino)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1: acetic acid / ethanol / 24 h / Reflux

2: palladium on activated charcoal; hydrogen / ethanol / 50 h / 20 °C / 7240.26 Torr / Autoclave; Inert atmosphere

3: trifluoroacetic acid / dichloromethane / 0.75 h / 0 - 20 °C

4: dichloromethane / -30 °C

With palladium on activated charcoal; hydrogen; acetic acid; trifluoroacetic acid; In ethanol; dichloromethane;