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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446796Generated: October 30, 2026

Potassium Carbonate → HCID 44537962, compound

https://huagongshe.com/reaction/446796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)quinolineHCID 20394—
Reactant3-(4-hydroxyphenyl)-4-(pyridin-4-yl)furan-2(5H)-oneHCID 136173335—
SolventDimethylformamideHCID 6228—
ProductHCID 44537962HCID 4453796219%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 3-(4-hydroxyphenyl)-4-(pyridin-4-yl)furan-2(5H)-one (700 mg, 2.76 mmol) in DMF (10 mL) was added K2CO3 (763.6 mg, 5.5 mmol) followed by 2-(chloromethyl)quinoline (711 mg, 3.32 mmol). The reaction mixture was then heated at 80° C. for 2 h, quenched with cold water, and extracted with EtOAc (2×25 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to obtain the crude product. The crude material was purified via silica gel column chromatography to afford 4-(pyridin-4-yl)-3-(4-(quinolin-2-ylmethoxy)phenyl) furan-2(5H)-one (190 mg, 19%) as a solid. 1H NMR (500 MHz, d6-DMSO): δ 8.61 (d, J=7.7 Hz, 2H), 8.42 (d, J=7.1 Hz, 1H), 8.04-7.96 (m, 2H), 7.81-7.76 (m, 1H), 7.65 (d, J=7.4 Hz, 1H), 7.60-7.54 (m, 1H), 7.44-7.36 (m, 4H), 7.11 (d, J=7.2 Hz, 2H), 5.40 (s, 2H), 5.34 (s, 2H). MS: M+H: m/z=395.1 and HPLC: 95%, (Condition-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481534B2
Source datasetuspto-grants-2013_07
ORD IDord-7a2a22d7a74c446e8d707c9d829c5722
Source noteuspto-grants-2013_07