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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 539889Erstellt: 25. Oktober 2026

Potassium Carbonate → ethyl 1-(2-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/539889

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2,4-DichloropyrimidineHCID 77531—
EduktHCID 178469911HCID 178469911—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl 1-(2-chloropyrimidin-4-yl)-3-methyl-1H-pyrazole-4-carboxylateHCID 8669898152,5%

Reaktionsschritte

To a solution of ethyl 3-methyl-1H-pyrazole-4-carboxylate (6.0 g, 38.9 mmol) in 50 mL of anhydrous N,N-dimethylformamide (DMF) were added potassium carbonate (10.8 g, 77.8 mmol) and 2,4-dichloropyrimidine (5.8 g, 38.9 mmol) at room temperature. The resulting suspension was stirred for 8 hours with monitoring a reaction with LC-MS or thin layer chromatography (TLC). Volatiles were removed and the residue was extracted with dichloromethane. The collected organic layer was washed with brine, 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 1 as a white solid (5.45 g, 52%); MS (ESI) m/z 267 [M+H]+, 1H NMR (300 MHz, CDCl3) δ 8.99 (s, 1H), 8.68 (d, 1H, J=5.4 Hz), 7.86 (d, 1H, J=5.4 Hz), 4.35 (q, 2H, J=7.2 Hz), 2.57 (s, 3H), 1.40 (t, 3H, J=7.2 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08871778B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-27eb9ebd561c4291b9dfe716dd9a22f7
Quellennotizuspto-grants-2014_10