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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539890Generated: October 26, 2026

Potassium Carbonate → 1-(2-Chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/539890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant1-ethyl-3-methyl-1H-pyrazole-4-carbaldehydeHCID 573203—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(2-Chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carbaldehydeHCID 7301231542.4%

Reaction Steps

To a solution of ethyl 3-methyl-1H-pyrazole-4-carbaldehyde (6.4 g, 58.0 mmol) in 60 mL of anhydrous N,N-dimethylformamide were added potassium carbonate (10.8 g, 77.8 mmol) and 2,4-dichloropyrimidine (8.64 g, 58.0 mmol) at room temperature. The resulting suspension was stirred for 14 hours at room temperature with monitoring a reaction with LC-MS or thin layer chromatography (TLC). The reaction mixture was diluted with ethyl acetate and washed with brine (×2). The collected organic layer was dried over anhydrous sodium sulfate and then concentrated in vacuo. The resulting residue was purified by silica gel chromatography using a mixture of heptanes and ethyl acetate to afford the desired intermediate 2 as a white solid (5.47 g, 42%); MS (ESI) m/z 223 [M+H]+, 1H NMR (300 MHz, CDCl3) δ 10.06 (s, 1H), 9.04 (s, 1H), 8.70 (d, 1H, J=5.4 Hz), 7.87 (1H, d, J=5.4 Hz), 2.59 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871778B2
Source datasetuspto-grants-2014_10
ORD IDord-d9c3f87b6352464680f0a2cf2c07943f
Source noteuspto-grants-2014_10