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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33875Generated: October 26, 2026

Potassium Carbonate → 2-[4-(5-Pyridin-4-yl-pyrazol-1-yl)-phenoxymethyl]-quinoline

https://huagongshe.com/reaction/33875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)quinolineHCID 20394—
Reactant4-(5-Pyridin-4-yl-pyrazol-1-yl)-phenolHCID 68576462—
SolventAcetoneHCID 180—
SolventSodium chloride; waterHCID 57417360—
Product2-[4-(5-Pyridin-4-yl-pyrazol-1-yl)-phenoxymethyl]-quinolineHCID 1166085769.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-(5-Pyridin-4-yl-pyrazol-1-yl)-phenol (82 mg) in acetone was added potassium carbonate (153 mg) and 2-Chloromethyl-quinoline (95 mg) and the reaction mixture heated at 60° C. for 18 h. The reaction mixture was poured into brine and extracted with ethyl acetate, dried magnesium sulfate, filtered and concentrated. Purification via combiflash MPLC provided the title compound (91 mg). 1H NMR (400 MHz, CDCl3) δ 8.51 (m, 2 H), 8.20 (d, J=8.7 Hz, 1 H), 8.06 (d, J=8.7 Hz, 1 H), 7.83 (d, J=7.1 Hz, 1H), 7.74 (m, 2H), 7.65 (d, J=8.7 Hz, 1 H), 7.57 (m, 1H), 7.20 (d, J=8.7 Hz, 2 H), 7.09 (d, J=5.8 Hz, 2H), 7.02 (d, J=9.1 Hz, 2H), 6.60 (d, J=1.7 Hz, 1H), 5.39 (s, 2H); MS: (M+H m/z=379.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429665B2
Source datasetuspto-grants-2008_09
ORD IDord-b53715596bbe47cb877f1ff216902a5e
Source noteuspto-grants-2008_09