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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714888Generated: October 30, 2026

Potassium Carbonate → (3R)-3-ethyl-1-(2-((2-methyl-1,3-thiazol-5-yl)amino)pyrimidin-4-yl)-2-oxopyrrolidine-3-carbonitrile hydrochloride

https://huagongshe.com/reaction/714888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant2-Methyl-1,3-thiazol-5-amineHCID 20829880—
Reactant(3R)-1-(2-chloropyrimidin-4-yl)-3-ethyl-2-oxopyrrolidine-3-carbonitrileHCID 117840665—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solventtert-ButanolHCID 6386—
Product(3R)-3-ethyl-1-(2-((2-methyl-1,3-thiazol-5-yl)amino)pyrimidin-4-yl)-2-oxopyrrolidine-3-carbonitrile hydrochlorideHCID 11784089310.3%

Reaction Steps

To a mixture of (3R)-1-(2-chloropyrimidin-4-yl)-3-ethyl-2-oxopyrrolidine-3-carbonitrile (100 mg) obtained in Step A of Example 8, 2-methyl-1,3-thiazol-5-amine (56 mg), potassium carbonate (110 mg) and dicyclohexyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2-yl)phosphine (58 mg) in tert-butanol (1.0 mL) was added tris(dibenzylideneacetone)dipalladium(0) (22 mg), and the mixture was stirred for 5 hr with heated under reflux. The insoluble substance was removed by filtration through Celite, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate). To a solution of the obtained compound (26 mg) in ethanol (2.0 mL) was added 1 M hydrochloric acid (80 μL), and the mixture was stirred at room temperature for 5 min. The solvent was evaporated under reduced pressure, and the residue was recrystallized (ethanol) to give the title compound (15 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187453B2
Source datasetuspto-grants-2015_11
ORD IDord-1d052eeb7c8e491db6e905342eba5eea
Source noteuspto-grants-2015_11