Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929689Generated: October 30, 2026

Potassium Carbonate → N-(3-(6-((3-Hydroxy-4-Morpholinophenyl)Amino)-1-(Tetrahydro-2H-Pyran-2-Yl)-1H-Pyrazolo[3,4-D]Pyrimidin-4-Yl)Phenyl)Acrylamide

https://huagongshe.com/reaction/929689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant5-Amino-2-morpholinophenolHCID 53905968—
ReactantN-(3-(6-chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)phenyl)acrylamideHCID 86677518—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solventtert-ButanolHCID 6386—
ProductN-(3-(6-((3-Hydroxy-4-Morpholinophenyl)Amino)-1-(Tetrahydro-2H-Pyran-2-Yl)-1H-Pyrazolo[3,4-D]Pyrimidin-4-Yl)Phenyl)AcrylamideHCID 11859100128.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

N-(3-(6-chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)phenyl)acrylamide (50 mg, 0.130 mmol), 5-amino-2-morpholinophenol (25.3 mg, 0.130 mmol) and potassium carbonate (45.0 mg, 0.326 mmol) were dissolved in t-BuOH (80 mL). 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene (3.01 mg, 5.21 μmol) and Pd2dba3 (2.386 mg, 2.61 μmol) were then added to the solution. The reaction mixture was refluxed at 100° C. for 12 h, and the reaction was monitored by TLC. Following completion of the reaction, the reaction mixture was allowed to cool, and the solvent was removed in vacuo. The resulting crude material was purified by flash chromatography (2% methanol/DCM) to yield the title compound (20 mg, 0.037 mmol, 28.3% yield) as yellow solid. Crude material was used without further purification and used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296703B2
Source datasetuspto-grants-2016_03
ORD IDord-5c9115cd0345448f86c1c1a82b351344
Source noteuspto-grants-2016_03