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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929682Generated: October 30, 2026

3-Acrylamidophenylboronic acid → N-(3-(2-chloro-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamide

https://huagongshe.com/reaction/929682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Acrylamidophenylboronic acidHCID 10321331—
Reactant2,4-dichloro-N-(3-fluorophenyl)pyrimidin-5-amineHCID 86677517—
ReactantN-(3-(2-((4-(3-fluoro-5-hydroxy-4-methylpiperazin-1-yl)phenyl)amino)-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamideHCID 118591002—
CatalystPalladiumHCID 23938—
ProductN-(3-(2-chloro-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamideHCID 71469247—

Reaction Steps

As an example, N-(3-(2-((4-(3-fluoro-5-hydroxy-4-methylpiperazin-1-yl)phenyl)amino)-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamide can be prepared according to Route I. Beginning with 2,4-dichloro-N-(3-fluorophenyl)pyrimidin-5-amine, a palladium catalyzed coupling reaction with (3-acrylamidophenyl)boronic acid provides N-(3-(2-chloro-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamide under mild conditions. Reaction of this product with 4-(4-aminophenyl)-6-fluoro-1-methylpiperazin-2-ol under palladium catalyzed aminolysis conditions can yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296703B2
Source datasetuspto-grants-2016_03
ORD IDord-2d8d4790749e42ee892afd5e3b97c983
Source noteuspto-grants-2016_03