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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424282Generated: November 2, 2026

3-Aminoquinoline → Ethyl (+/-)-4-(4,4,4-trifluoro-1-(quinolin-3-ylamino)butyl)benzoate

https://huagongshe.com/reaction/1424282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminoquinolineHCID 11375—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantEthyl(+/-)-4-(4,4,4-trifluoro-1-((methylsulfonyl)oxy)butyl)benzoateHCID 86718838—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductEthyl (+/-)-4-(4,4,4-trifluoro-1-(quinolin-3-ylamino)butyl)benzoateHCID 86718839—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl(+/−)-4-(4,4,4-trifluoro-1-((methylsulfonyl)oxy)butyl)benzoate (123 mg, 0.347 mmol) in acetonitrile (1.74 mL) was added 3-amino quinoline (60.6 mg, 0.416 mmol), followed by potassium phosphate (155 mg, 0.694 mmol). The resulting mixture was heated to 60° C. for 20 hours. The reaction mixture was cooled to room temperature, diluted with water (20 mL), and extracted with ethyl acetate (3×20 mL). The combined organic layers were dried over Na2SO4 and filtered, and the filtrate was concentrated under reduced pressure. Purification by silica gel flash chromatography (ethyl acetate/heptane) gave ethyl(+/−)-4-(4,4,4-trifluoro-1-(quinolin-3-ylamino)butyl)benzoate. 1H NMR (400 MHz, CDCl3) δ 8.51 (d, J=2.5 Hz, 1H), 8.06 (d, J=8.4 Hz, 2H), 7.92 (d, J=7.8 Hz, 1H), 7.50-7.44 (m, 3H), 7.44-7.35 (m, 2H), 6.81 (d, J=2.5 Hz, 1H), 4.62-4.54 (m, 1H), 4.44-4.33 (m, 3H), 2.36-2.10 (m, 4H), 1.38 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927577B2
Source datasetuspto-grants-2015_01
ORD IDord-2b6913464ea645cca9366577a949a9ae
Source noteuspto-grants-2015_01