Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500271Generated: October 29, 2026

Potassium Carbonate → tert-butyl[3-(2-aminopyrimidin-5-yl)-1H-pyrazol-1-yl]acetate

https://huagongshe.com/reaction/500271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant2-Amino-5-bromopyrimidineHCID 231310—
Reactant1H-Pyrazole-5-boronic acidHCID 11251979—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Producttert-butyl[3-(2-aminopyrimidin-5-yl)-1H-pyrazol-1-yl]acetateHCID 90849675—

Reaction Steps

To a solution of 1H-pyrazol-5-ylboronic acid (0.2 g, 2 mmol) in N,N-dimethylformamide (1.0 mL) were added 1,1-dimethylethyl bromoacetate (0.38 g, 2 mmol) and potassium carbonate (0.74 g, 0.0054 mol). The reaction mixture was stirred overnight at RT. To the reaction mixture was added 5-bromopyrimidin-2-amine (0.40 g, 2.3 mmol) and tetrakis(triphenylphosphine)palladium (0.1 g, 0.09 mmol). The resulting mixture was stirred at 100° C. for 2 h. After cooling to RT, the reaction mixture was extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated. The residue was purified by RP-HPLC to afford the desired product. LCMS: (M+H)=276.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-0f2b61a863b44e03adc46c6492ad2357
Source noteuspto-grants-2010_08