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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295589Generated: October 27, 2026

Diisopropylethylamine → 7-{1-[2-(2-Methylquinolin-5-yloxy)ethyl]piperidin-4-yloxy}-3,4-dihydro-1H-quinolin-2-one

https://huagongshe.com/reaction/1295589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-(2-Bromoethoxy)-2-methylquinolineHCID 11737192—
Reactant7-(Piperidin-4-yloxy)-3,4-dihydroquinolin-2(1H)-oneHCID 17965144—
SolventIsopropanolHCID 3776—
Product7-{1-[2-(2-Methylquinolin-5-yloxy)ethyl]piperidin-4-yloxy}-3,4-dihydro-1H-quinolin-2-oneHCID 1796514346.3%

Reaction Steps

7-(Piperidin-4-yloxy)-3,4-dihydro-1H-quinolin-2-one (0.064 g, 0.25 mmol) and 5-(2-bromoethoxy)-2-methylquinoline (0.069 g, 0.25 mmol) were mixed together in propan-2-ol (20 mL), N,N-diisopropylethylamine (0.336 g, 2.6 mmol) added and the mixture heated at reflux for 48 h. The volatiles were removed by evaporation to dryness under reduced pressure and the residue partitioned between ethyl acetate and saturated NaHCO3 aq. The phases were separated, the organic phase washed with water, dried (MgSO4) and evaporated to dryness under reduced pressure. Chromatography on SiO2, eluting with a gradient of ethyl acetate in 60–80° C. petroleum ether, gave the title compound (0.05 g, 45%) as a white solid, after trituration under 60–80° C. petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244726B2
Source datasetuspto-grants-2007_07
ORD IDord-8b0f2b21fd8348bfb79de6df7d1f2fdb
Source noteuspto-grants-2007_07