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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852954Generated: November 2, 2026

Potassium Phosphate, Tribasic → 7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidin-5(6H)-one

https://huagongshe.com/reaction/1852954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant7-Chloroimidazo[1,2-c]pyrimidin-5-olHCID 21320102—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventIsopropanolHCID 3776—
Product7-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-c]pyrimidin-5(6H)-oneHCID 6745193976%

Reaction Steps

To a mixture of 7-chloroimidazo[1,2-c]pyrimidin-5(6H)-one (Preparation H, 10.0 g, 59.0 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (19.0 g, 88.5 mmol) and XPHOS (2.81 g, 5.90 mmol) in isopropyl alcohol (400 mL) was added 2M K3PO4 (88.5 mL, 177 mmol). The mixture was purged with N2 for 15 minutes with vigorous mixing and Pd2dba3 (2.70 g, 2.95 mmol) was added. The mixture was heated at reflux under a N2 atmosphere for 20 hours. The mixture was charged additional 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (6.00 g) and Pd2dba3 (1.00 g) and heated at reflux for an additional 20 hours. The mixture was cooled to ambient temperature and concentrated to an aqueous syrup. The syrup was partitioned into H2O (500 mL) and 50% EtOAc-hexanes (250 mL) and mixed. The mixture was filtered through filter paper and the orange organic layer was removed. The aqueous layer was washed with 50% EtOAc/hexanes and was cooled on an ice bath. The solution was treated with concentrated HCl to pH 6 with stirring and the resulting fine precipitate was collected, washed with H2O and Et2O and dried under vacuum to provide the title compound (9.65 g, 76% yield) as faint grey solid. MS (apci) m/z=216.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962596B2
Source datasetuspto-grants-2015_02
ORD IDord-3b6affd909b54a9fbf3f5c661ef97018
Source noteuspto-grants-2015_02