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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925030Generated: October 26, 2026

5-Bromo-2,4-dimethoxypyrimidine → 2,4-bis-(methyloxy)-5-(1-methyl-1H-pyrazol-4-yl)pyrimidine

https://huagongshe.com/reaction/1925030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2,4-dimethoxypyrimidineHCID 255719—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2,4-bis-(methyloxy)-5-(1-methyl-1H-pyrazol-4-yl)pyrimidineHCID 59448365—

Reaction Steps

5-bromo-2,4-bis(methyloxy)pyrimidine (commercially available from Aldrich, 500 mg, 2.283 mmol) was dissolved in 1,2-Dimethoxyethane (DME) (5 ml). Pd(Ph3)4 (132 mg, 0.114 mmol) was added and the reaction mixture was stirred at room temperature for 15 min. 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (commercially available from Maybridge, 997 mg, 4.79 mmol) and 1M/H2O sol. of NaHCO3 (5 ml, 5.00 mmol) were added. After 2 h stirring at 90° C., the reaction mixture was cooled at room temperature, diluted with water (5 ml) and extracted with DCM (3×10 ml). The obtained residue was purified by flash chromatography first eluting with cyclohexane/EtOAc 4:1 then with 1:2 cyclohexane/EtOAc. 483.7 mg of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178549B2
Source datasetuspto-grants-2012_05
ORD IDord-3acba802381e4b178d38ae626f07c623
Source noteuspto-grants-2012_05