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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257818Generated: October 27, 2026

Sodium Carbonate → Tert-butyl 4-(2-aminopyrimidin-5-yl)benzoate

https://huagongshe.com/reaction/1257818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-bromopyrimidineHCID 231310—
Reactant(4-((Tert-butoxy)carbonyl)phenyl)boronic acidHCID 2773301—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(2-aminopyrimidin-5-yl)benzoateHCID 6722525186.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

Sodium carbonate (0.636 g, 6.0 mmol) in water (2.0 mL) was added to a mixture of 5-bromopyrimidin-2-amine (0.348 g, 2.0 mmol), [4-(tert-butoxycarbonyl)phenyl]boronic acid (0.533 g, 2.4 mmol) and tetrakis(triphenylphosphine)palladium (69 mg, 0.06 mmol) in ethanol (3 mL) and toluene (3 mL). The mixture was heated at 120° C. for 3 h. After cooling to RT, the mixture was diluted with EtOAc and washed with water and brine. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to afford the desired product (470 mg, 86.6%) which was directly used in next step. LCMS: (M+H)=272.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-8cdfd873ee8a44ecaacbb4a34b35256d
Source noteuspto-grants-2013_06