Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266956Generated: November 3, 2026

Water → Isobutyl 4-(4-(2-(difluoromethyl)phenyl)pyrimidin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2266956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantIsobutyl 1-(4-chloropyrimidin-2-yl)piperazine-4-carboxylateHCID 58857071—
Reactant2-[2-(Difluoromethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 59264588—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
ProductIsobutyl 4-(4-(2-(difluoromethyl)phenyl)pyrimidin-2-yl)piperazine-1-carboxylateHCID 16097306—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of the isobutyl 4-(4-chloropyrimidin-2-yl)piperazine-1-carboxylate 8a and 2-(2-(difluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 11a (1.2 eq) in acetonitrile was added Pd(PPh3)4 (0.10 eq), K2CO3 (2 eq) and water. The vial was sealed and heated by microwave irradiation at 120° C. for 15 minutes. The solvent was evaporated and the residue was dissolved in DMF and purified by reverse phase HPLC (using 10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA) to give 24. m/z 391.1 (M+1), r.t: 3.59 (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858786B2
Source datasetuspto-grants-2010_12
ORD IDord-6d0acf4e72944227b563d2a4c7a3fd83
Source noteuspto-grants-2010_12