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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245231Generated: October 26, 2026

Acetonitrile → Isobutyl 4-(2-(2-hydroxyphenyl)pyridin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2245231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734622—
ReactantIsobutyl 4-(2-chloropyridin-4-yl)piperazine-1-carboxylateHCID 58853192—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductIsobutyl 4-(2-(2-hydroxyphenyl)pyridin-4-yl)piperazine-1-carboxylateHCID 135547506—

Reaction Conditions

Temperature120 °C

Reaction Steps

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-phenol (25/μL, 120 μmol), 3a (30 mg, 100 μmol), Pd(Ph3P)4 (12 mg, 10 μmol), K2CO3 (28 mg, 200 μmol), CH3CN (900 μL), and H2O (100 μL) were sealed in a microwave vessel and heated by microwave irradiation at 120° C. for 15 minutes. The reaction was filtered and purified by reverse phase HPLC to give compound 1. (10%-99% CH3CN/H2O), (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA). LCMS: m/z 356.1 (M+H)+ at 2.24 minutes (10%-99% CH3CN/H2O), (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683065B2
Source datasetuspto-grants-2010_03
ORD IDord-f70556166651423a8db3cdd77edd78e8
Source noteuspto-grants-2010_03