HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Acrylamidophenylboronic acid → N-(3-(2-chloro-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Acrylamidophenylboronic acid | HCID 10321331 | — |
| Reactant | 2,4-dichloro-N-(3-fluorophenyl)pyrimidin-5-amine | HCID 86677517 | — |
| Reactant | N-(3-(2-((4-(3-fluoro-5-hydroxy-4-methylpiperazin-1-yl)phenyl)amino)-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamide | HCID 118591002 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | N-(3-(2-chloro-5-((3-fluorophenyl)amino)pyrimidin-4-yl)phenyl)acrylamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296703B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-2d8d4790749e42ee892afd5e3b97c983 |
| Source note | uspto-grants-2016_03 |